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Postdoc & PhD Jobs

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Latest Postdoctoral Jobs
1015912| Atlantic Counseling & Consultation, Inc.| LICSW / LMHC / PhD.| Company Description:

Multidisciplinary practice established in 1982.

Job Description:

Two licensed Clinicians, adult and child, 3 years post license experience wanted to join our well established, 17 clinician multidisciplinary group practice located in South Weymouth. Interesting case loads, great administrative and billing support, inclusion on our insurance panels, plentiful referrals and beautifully decorated offices.

Let us manage the headaches of the practice while you focus on the clinical work. Compensation to be discussed at interview.

Come and join our team.

Saturdays available.

P/T and F/T available.
1013645| FYZICAL Therapy & Balance Centers| Project Management Specialist| Company Description:

FYZICAL West Palm Beach is Palm Beach County's leading provider of physical therapy, rehabilitation, and sports medicine services.

We are a values driven organization seeking to provide the highest caliber of rehabilitative services possible. Our team of physical therapists strives to return patients to an optimal level of health and well-being, in addition to helping them resume a more fruitful lifestyle. FYZICAL embraces a patient-centric philosophy of care. The patient is our primary concern, from respecting your time, to providing you with a professional, friendly, and inviting atmosphere.

We take great pride in providing a responsiveness to our patients' needs that is unparalleled in the community.

Job Description:

Physical Therapy - Opportunity of A Lifetime

Join a world class team of experts and help reshape the landscape of outpatient physical therapy in the United States. As a Project Manager, you will use your therapy skills and expertise as a tool to change the lives of therapists and their patients throughout the United States. Must be proficient with writing skills, be analytical and have the ability to concisely articulate thoughts, ideas and concepts in writing. Proficiency with word, excel,&power point a plus. PTA's, PT's (MPT, DPT, PhD) and other professionals welcome to apply. Culture and values are the driving force behind our organization so If you are a team player who is detail oriented, hard working, pleasant and fun to be around, call us today. Enjoy tremendous opportunity for advancement!
1016336| Northrop Grumman| Engineer Systems Analyst 4 Engineer / 14-626A-AAT| The MET-I program is currently seeking a Systems Engineer/Analyst 4 to be located in Huntsville, AL. Northrop Grumman Information Systems (NGIS) was selected by the U.S. Missile Defense Agency to participate on the Missile Defense National Team. This team was chartered to develop a Ballistic Missile Defense System for the United States. Air&Missile Defense Systems (A&MDS) serves as Northrop Grumman Information Systems' focal point for all activities associated with missile defense, including Command, Control, Battle Management and Communications (C2BMC), simulation&modeling, systems engineering, and target discrimination.

- Individual will perform end-to-end analysis of the Ballistic Missile Defense System (BMDS) supporting the systems
engineering process for the Missile Defense Agency (MDA).
- Individual will perform BMDS performance analyses utilizing large-scale complex BMDS modeling and simulation tools
and utilize the results to support system engineering products for MDA.
- Individual will also perform development, updates, and benchmarking/anchoring of BMDS M&S tools, as necessary
to support system analysis tasks. Individual will coordinate analysis activities and products with functional group leads,
senior management, and government personnel responsible for executing analysis tasks.
- The individual will document analysis results in reports and briefings to be presented to the Missile Defense Agency Engineering Team - Industry (MET-I) and Missile Defense Agency (MDA) representatives.
- Individual may perform as a principal investigator.
- Individual may lead analysis teams.
""ERAPIAMD""


Qualifications:
Basic Qualifications:Typical Minimum Education / Experience: 9 Years with Bachelors in in an engineering classification, mathematics or physics or 7 Years with Masters; 4 Years with PhD. Individual must have a technical background in numerical modeling and simulation, using a high level programming language such as MATLAB, Python, FORTRAN, or similar language environment, and any of the following: EO/IR sensors, RF/Radar sensors, missiles/interceptors, threats, discrimination, detection/tracking, or Command and Control (e.g., C3I, C4I, etc.). Individual must possess good communication skills. Capable of working both independently and in a team environment. Individual must have some demonstrated team leadership experience.

Preferred Qualifications:Demonstrated discrimination experience using BMDS EO/IR assets ( e.g ., PTSS, Halo, SM-3, EKV, etc .) and/or BMDS radar assets (e.g., AN/TPY-2, SBX, SPY-1, etc). Experience in some or all of Ballistic missile defense system, Aegis Weapons Systems, Ground-based Midcourse Defense (GMD), Fire Control (FOM, GFC), C2BMC, BMDS sensors (EO/IR/RF), kill vehicles, interceptors, countermeasures, counter-countermeasures, or threats. Systems engineering experience with large, complex systems. Candidates with active TS clearance preferred; if candidate has SECRET clearance, reinvestigation date less than 5 years old is preferred and candidate must be able to obtain a TS clearance.

Northrop Grumman Corporation is a leading global security company providing innovative systems, products, and solutions in unmanned systems, cybersecurity, C4ISR, and logistics and modernization to government and commercial customers worldwide.

Northrop Grumman is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action-Employer, making decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected class. For our complete EEO/AA statement, please visit


Connect with our Talent Community:



Company Description:

Northrop Grumman is a leading global security company providing innovative systems, products and solutions in unmanned systems, cyber, C4ISR, and logistics and modernization to government and commercial customers worldwide. Please visit for more information.

© 2014 Northrop Grumman is committed to hiring and retaining a diverse workforce. We are an Equal Opportunity/Affirmative Action Employer. U.S. Citizenship is required for most positions. For our complete EEO/Diversity statement, please visit

1015688| NBS Enterprises, LLC| ESW06: Software Engineer - Principal II ... S3| Company Description:

NBS Enterprises creates competitive advantages. We isolate and overcome constraints to deliver performance value for all involved: you, your customer, and your employees. We break current market staffing trends with price-sensitive strategies solutions.

Our goal is to work in partnership with you, our client, become a trusted advisor and teammate to establish a relationship that provides you and your team with a competitive advantage at both the contract and at the task order levels. NBS' innovative 'Triangle' approach to staffing support provides you, your customer, and your future employee a risk mitigation solution that is second to none.

Job Description:

ESW06: Software Engineer - Principal II

Ten (10) or more years of software development experience required. [A Master's degree in a related discipline may substitute for two (2) years of experience. A PhD may substitute for four (4) years of experience.]

Bachelor's degree in Software Engineering, Computer Science or a related discipline is required.

Additional Requirements:
Experience leading multiple software development teams. Experience developing system performance, availability, scalability, manageability and security requirements for mid- to large-scale programs.

Experience with cloud computing, multimedia storage, knowledge databases and data-mining analytics

Agile development methodology experience required.

Certifications:
Agile software development methodology certification (e.g. SCRUM Master) highly desired.

-----------------------------------------------------------

Clearance Requirements: TS/SCI Cleared

-----------------------------------------------------------

All levels of Software Engineer will have the skills listed below. Each level may have additional education, skill and/or experience requirements.

The Software Engineer develops, maintains, and enhances complex and diverse software systems (e.g., processing-intensive analytics, novel algorithm development, manipulation of extremely large data sets, real-time systems, and business management information systems) based upon documented requirements.

Software Engineering tasks include:

Design and develop new software.

Maintain existing software and resolves software problem reports.

Modify existing software to add new features.

Perform individually and as part of a team.

Utilize software development and software design methodologies appropriate to the development environment and in compliance with customer and industry lifecycle development approaches.

Develop, execute and document software testing, including test cases.

Perform software requirement analysis, derivation and allocation.

Provide input to the software components of system design to include hardware/software trade-offs, software reuse, application security, and use of Commercial Off-the-shelf (COTS)/Government Off-the-shelf (GOTS) in place of new development.

Provide input to hardware (COTS/GOTS/capacity/etc.) recommendations.

Prepare software documentation, including user guides.

Required skills include:

Active Top Secret/Sensitive Compartmented Information (TS/SCI) security clearance required.

U.S. Citizenship required.

Demonstrated experience and/or familiarity with one of more of the following: Java, Perl, Ruby, Python, HTML, C, C++, .NET, ColdFusion, Adobe, etc.

Demonstrated experience and/or familiarity with one of more of the following: SQL, Oracle, MySQL, JBDC, etc.

Demonstrated experience and/or familiarity with one of more of the following: Windows, Linux, Apache, TomCat, Ozone Widgets, Spring, Struts, JUnit, Hibernate, etc.

Desired skills include:

Experience with Agile development methodology.

Experience with software configuration management and control tools (e.g., CVS, Eclipse, ClearCase, etc.)

Experience with automated testing tools (e.g., RSpec, Cucumber, etc.)

Certifications:

DoD 8570.1-M Compliance at IAT Level I (e.g., Certified Information Systems Security Professional (CISSP)) certification highly desired
1016664| Cranleigh Scientific| Bioinformatics Specialist-Oracle-Drug Discovery-c.£50k-Cambs.| Bioinformatics Specialist-Oracle-Drug Discovery-c.£50k-Cambs.-T-SQL-ActivityBase-VBA-ChemFinder

A leading pharmaceutical company are expanding and require an experienced Bioinformatics Specialist to join their team. You will be responsible for the development, implementation and maintenance of chemical/biological information systems within Research and to provide hands on support for key scientific information systems. You will have significant experience both in database management and biology.

The Role

This full time role is responsible for the development, implementation and maintenance of chemical/biological information systems within Research and provides hands on support for key scientific information systems. Ideally suited to a scientist with drug discovery experience and expertise in using database applications to manage and analyse chemical and biological data.

Responsibilities

? Maintain and develop discovery research databases
? Collaborate with key scientific personnel to optimise and develop new scientific
information systems and reporting tools.
? Maintain protocols within ActivityBase; provide and implement updates, new
studies and protocols in accordance with end user requirements.
? Implement improvements in template design and design new templates for use in
assays and HTS screening through liaison with end users in Chemistry and
Biology.
? Provide reporting templates; enhance existing formatting tools and develop new
formatting tools for use in Chemistry and Biology within ActivityBase.
? Support the development and rollout phases of new information systems.
? Train users on existing and/or new information systems.
? Liaise with IT team to ensure availability of research reporting tools and
applications to aid workflows.
? Extract and manage data from a variety of sources e.g. legacy data, commercial
chemical libraries etc. and incorporate into ActvityBase and other systems
? General administration of scientific database systems e.g. data dictionary upkeep
and database purging.

Skills&Experience

Education/Work Experience

? Minimum qualification: BSc/MSc in a relevant scientific discipline. Ideally
candidates should hold a PhD or other post graduate qualification.
? > 5 years post graduate experience (significant industry experience is highly
preferred)
? Strong relational database development skills (Oracle preferred) e.g.: schema
design, PL/SQL, T-SQL, data warehousing, ETL in a scientific environment
? Management of biological assay data, preferably with experience of ActivityBase
? Experience of providing .Net and/or VBA data reporting tools within a MS Office
environment
? Familiarity with the drug discovery process and experience with drug discovery
research tools such as ActivityBase, ChemFinder or ISISBasePersonal Competencies
? Confident communication and presentation skills
? Maintains an active awareness of new and developing technologies
? Works both independently and in collaboration within others
? Plans ahead and is proactive in identifying and troubleshooting potential
obstacles.
? Meticulous with excellent analytical and organisational skills.
? Can deal with tight deadlines and changing priorities
? A team player with the ability to work in a multi-disciplinary environment
? Reliable, professional and conscientious attitude

Other Information

This is a full time (37.5 hours a week), permanent position.

Bioinformatics Specialist-Oracle-Drug Discovery-c.£50k-Cambs.

1016665| Reed Scientific (NEW)| Senior Scientist - Prenatal Testing| Senior Scientist
Cambridge
Competitive salary and benefits
Permanent&Full Time

My client are a leading provider of translational genomics research tools and they are looking for an experienced Molecular Biologist to help create innovative molecular diagnostic products.

The role will involve leading a new company initiative related to prenatal testing. You will be involved with the technical realisation of new product ideas, and will then take an active part in the early concept design and development of these ideas for future products and services. Additional duties will also include creating product related protocols and SOPs, working closely with the commercial team to develop product development strategy and completing scientific understanding of the prenatal testing field to progress innovative product ideas.

The ideal candidate will be educated to PhD level and possess between 3-7 years post-doc work experience. You must have a solid understanding of NGS technology, as well as a strong Bioinformatics knowledge, particularly with NGS pipelines. You will possess an array of experience with different Molecular Biology techniques including digital PCR, qPCR and with DNA/RNA. Previous product development and any prenatal testing experience would be highly desirable.

If this sounds like a role that you are interested in and would like more details then please get in touch on Phone number removed or via email at

Reed Specialist Recruitment Limited is an employment agency and employment business.
1013837| Northrop Grumman| Software Defined Radio Engineer 3| Northrop Grumman Information Systems sector is seeking Electrical/Software Engineers to join our team to perform leading-edge research, development, and integration of real-time Software Define Radio (SDR) and Wireless Protocols to
solve the most complex communication and radio navigation (GPS) receiver technical challenges. The candidate will be part of the development team operating in a dynamic, fast paced environment located in Beavercreek, OH.

• The qualified applicant will be involved in the full life cycle of GPS Signal Processing Algorithms integration (Design, Development, Implementation, and Testing). Key responsibilities include: implementing GPS and waveform algorithms
in embedded signal processors / FPGA's including simulation, coding, optimization and testing system and subsystem requirements analysis, definition, and validation; systems and subsystems design architecture, integration and verification testing; leading or supporting technical collaboration among systems, hardware and software design functions; resolution of technical problems that cross functional domain areas of hardware/software and development of systems related documentation. Candidate will apply the appropriate standards, processes, procedures and tools throughout the system development life cycle to support the generation of such engineering applications and products. Also he/she will be
expected to interface with customers, suppliers, application users and other technical support personnel.

Roles and Responsibilities:
• Develop and document requirements and design.
• Code and Unit Test software.
• Integrate software radio techniques onto hardware platform.
• Develop Integration and Test procedures.
• Configuration control in a LINUX and VxWorks environments.
• Support for preparation and presentation of formal technical reviews.

Qualifications:
Basic Qualifications:
• Bachelors Degree in Electrical Engineering and/or Computer Engineering plus 5 years of experience. Masters Degree
and 3 years of experience or PhD and 1 years of experience.
• The candidate must have design experience of software defined tactical radios
• Design experience with Signal Processing, DSP design, and algorithmic code development and the integration of SDR
functions to digital hardware, preferably Xilinx System-on-a-Chip FPGAs.
• Must be able to develop and document designs, simulations, analysis and test results.
• Must be able to work independently in a lab and perform initial hardware check-out and debug.
• Experience with RTL code development using Verilog or VHDL is required
• Programming language experience to include: C, C and scripting
• Develop in LINUX and VxWorks environments.
*Ability to obtain a secret security clearance required
Travel up to 10% for engineering analysis, test, and customer technical exchanges

Preferred Qualifications:
•Com/Nav design experience
• Knowledge of digital communications theory, including detection, estimation, and demodulation
• Knowledge of GPS receiver design
• Experience conducting end-to-end RF system analysis including link budget development, channel modeling, and RF
block diagram development
• Software modeling and simulation, MATLAB skills
• Experience with real-time signal processing algorithms on Linux-based SDR platforms
• Experience with firmware/VHDL design including Xilinx environments
• Embedded software development and test.
• Experience with DoD engineering processes, including systems and software component requirements derivation
• Experience with Matlab, System Generator or similar DSP design and simulation tools is a plus.
• Familiarity with design Configuration Management and Quality Control Processes is desired.
• Strong verbal and written communication skills
• Strong interpersonal skills
• Strong analytical skills

Northrop Grumman Corporation is a leading global security company providing innovative systems, products, and solutions in unmanned systems, cybersecurity, C4ISR, and logistics and modernization to government and commercial customers worldwide.

Northrop Grumman is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action-Employer, making decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected class. For our complete EEO/AA statement, please visit


Connect with our Talent Community:



Company Description:

Northrop Grumman is a leading global security company providing innovative systems, products and solutions in unmanned systems, cyber, C4ISR, and logistics and modernization to government and commercial customers worldwide. Please visit for more information.

© 2014 Northrop Grumman is committed to hiring and retaining a diverse workforce. We are an Equal Opportunity/Affirmative Action Employer. U.S. Citizenship is required for most positions. For our complete EEO/Diversity statement, please visit

1014531| The Judge Group| Asc. Dir., Medical Science Liaison| Company Description:

Founded in 1970 by Martin E. Judge Jr., The Judge Group is a professional services firm offering Technology Consulting, Enterprise-Wide Staffing and Corporate Training.

The Judge Group has long believed in strong companies and the talented people who help them grow. Forty years of experience have taught us how to best address the cultural and economic needs of our clients, expertly assist candidates in navigating through their own unique career progressions, and create, maintain, and nurture valued community partnerships.

Job Description:

Our client is seeking an Associate Director, Medical Science Liaison (MSL) for a new six member field-based team. Residing in the Medical Affairs Department and working with cross-functional teams, the MSL will apply scientific experience, knowledge, and skills to execute against strategic plans for emerging customers, including integrated delivery networks. Responsibilities include establishing and maintaining business relationships, advancing Company initiatives, presenting data, and eliciting insights from key influencers, decision-makers and clinical leaders. Scientific interactions will focus on data and information pertaining to company portfolio and therapeutic areas. For internal stakeholders, the MSL will serve as a medical and subject area expert. The MSL is expected to advance actionable information to cross-functional leaders within the company, and inform strategy based on the insights and values of customers and contacts. Topics may include unmet product and service needs or medical and research issues. The MSL can have considerable impact through participation in the proposal, planning and implementation of cross-functional initiatives. An advanced degree is required: MD/ Pharm.D./DO/PhD/Advanced Practice Nurse with MSN. Individuals must have a minimum of three years of pharmaceutical, biologics, or device industry experience in a Medical Affairs or MSL role. Clinical experience, preferably in a healthcare system, is preferred. This may include, but is not limited to: hospitalist, medical director, clinical pharmacy specialist, pharmacy manager, healthcare administrator, or disease state management program leader. Candidates should also be locally, regionally, and/or nationally recognized leaders through appointments, certifications, or memberships. Clinical knowledge and experience in the field of multi-disciplinary pain care is a plus. Working knowledge of US healthcare systems and regulatory and commercial compliance issues relating to the pharmaceutical industry is required. Individuals should possess social intelligence, excellent verbal and written communication skills including experience in public speaking and group facilitation. Candidates must be self-motivated and able to prioritize and work effectively in a constantly changing environment. A strong commitment to teamwork is required. Computer skills including Excel, Word, Power Point and web conferencing software are expected. A willingness and ability to travel frequently is required. Overnight travel and some weekend will be necessary. Applicants must live in close proximity to a major airport and have a valid U.S driver's license in good standing. The MSL will report to a Director, MSL, who will guide in the planning and implementation of territory strategy, scientific messages and initiatives.
1014899| US Memory Centers| Psychologist | Part Time or Full Time | Nanuet NY| Company Description:

Who, will you be joining:

A team of colleagues committed to clinical excellence, compassionate care, and professional integrity; an organization that welcomes your participation in a collaborative" approach to the integration of psychological services in multidisciplinary settings. The group that provides individualized training, ongoing clinical supervision, and professional development workshops in all our service domains.

Job Description:

I am pleased to call to your attention to available Career opportunities for licensed clinical social workers&psychologists (part or full time) with US Memory Centers. For the past nineteen years our group has been providing psychological services, neuropsychological/cognitive rehabilitation, and behavioral medicine services to residents to over 300 senior living facilities throughout the United States.

Where: Our continued growth has created openings in several prestigious Assisted Living facilities in the Rockland County area.

What do we provide:

1) We offer a clinically as well as a financially rewarding position
2) A very flexible work schedule
3) Provide training in gero-psychology under the supervision of our prominent clinical directors.
4) Opportunities to serve as a supervising psychologist in our Post-doctoral training program in behavioral medicine and gero-psychology to help develop license-eligibility.

Requirements:

1) PhD or PsyD,
2) A current New York license
3) Malpractice insurance
4) Good computer skills
5) Laptop or tablet
1017660| Edda Technology| Research Scientist| Company Description:

Company Introduction:

Excellent opportunity with a dynamic, growing medical technology solution company.

EDDA Technology is an innovative clinical computer solution provider in diagnostic imaging and analysis. EDDA offers a series of new generation software products to enable early detection of diseases, and to enhance efficiency and precision in diagnosis and treatment. EDDA is headquartered in Princeton, New Jersey, and has a subsidiary in Shanghai, China. ()
Compensation/ Benefits
EDDA offers a competitive salary, performance based incentive stock options, and excellent benefits including medical and dental insurance, vision care, 401k plan, section 125 health and dependent care (flexible spending) accounts, and paid vacations.

Job Description:

Job Description:

Multiple Research Scientist positions are available at EDDA Technology, Princeton, NJ. Responsibilities include:

Design, implementation, and verification of medical imaging analysis algorithms on 3D and 2D images;
Working with team members to integrate the algorithms into products;
Conforming to the Company's standard/procedure of product development;
Efficiently communicating with project managers and team members on the execution;
Other job responsibilities as assigned by the management.

Required qualifications (multiple positions, qualify on either of the first 2 requirements and the rest):

Strong algorithm development skills with in-depth knowledge on medical image analysis/segmentation, real-time processing, image registration, and parallel programming; or
Working knowledge on 2D/3D computer graphics and visualization, volume rendering, GUI design, Qt programming, .NET programming;
Strong problem solving skills with quick implementation and verification;
Experience with clinical/technical applications and medical devices, such sensors, scanners, and ultrasounds.
5+ years image analysis algorithm development experience with excellent software engineering skills in using C/C++ ; 1+ years industrial experience preferred;

Good communication skills;

Strong team player and highly self-motivated individual with desire and ability to learn quickly;
PhD in CE/EE/CS/Physics/Bio-Engineering.

Desired qualifications:

Hands-on experience and knowledge with DICOM a plus;
Knowledge of TCP/IP socket programming a plus;
1017452| NonStop Pharma Recruitment| Scientific Director - Clinical Pharmacology - South East UK| IM/92989/A

Scientific Director - Clinical Pharmacology - South East UK

I'm seeking a Scientific Director within the Clinical Pharmacology area to join a large international Pharma company who offer. You will be responsible for the development, adaptation and integration of new and innovative strategies in the Clinical phase of development, while also overseeing the preclinical and translational phases, and identifying potential issues.

Highly respected for its working environment, ethical standards, and working practices my client is well known for encouraging and enabling professional development, making this a highly attractive position with excellent benefits.

Ideally you will hold an M.Sc. or a PhD in a related area, and have a minimum of 10 years experience in the Clinical Pharmacology area and have a proven ability to design, supervise and interpret various types of in studies.

Please send your CV in an MS WORD format to me, Iain Morrison, for a confidential discussion or to apply for this position. Either click 'Apply now' or send your CV Email address removed or call me on , or Phone number removed I am a specialist recruiter in the Pharmacology arena, based in Switzerland.

Key Skills: Pharmacology, Safety Pharmacology, Pre-clinical drug safety, DMPK, PKPD, PBPK, ADME, LADME, Pharmacokinetics, Pharamcodynamics, Drug:Drug interaction, Durg Drug interactions, Modelling and simulation, WinNonlim
1017437| Caresoft Global Limited| Research Manager (Virtual Engineering)| Research Manager to provide research leadership and undertake independent and/or collaborative research for the virtual engineering team and to contribute to research strategies within the HSSMI.

Principal Accountabilities (Major end results the job is expected to achieve);

Lead advanced manufacturing research themes using, or developing appropriate methods and/or techniques.
Author manufacturing research proposals to secure commercial and research funding
Deal with contract negotiation and financial allocation with research collaborators.
Take responsibility for allocated team's delivery and output.
Ensure research outcomes and associated 'workplans' are delivered.
Management of a team of Research Associates, Graduates and Students to include supervision and involvement in recruitment, induction, training and coaching to develop their research techniques.
Develop individual training plans for members of staff
Allocate resources to project
Provide guidance and support to students associated with the research area.
Develop a network and disseminate / exploit knowledge of the research theme
Manage a portfolio of Industrial and Academic members
Actively develop appropriate external contacts to facilitate future collaboration and funding opportunities.
Produce high‐quality peer reviewed research reports and/or publications
Develop and deploy commercialisation plans.
Exploit arising intellectual property.
Disseminate knowledge to HSSMI members and the wider academic community.
Maintain high quality of outputs
Develop, deploy and ensure compliance with relevant internal ISO procedures

Skills/Experience Required
Professional expertise in Manufacturing
Engineering with specialization in Virtual Engineering.
Extensive experience in factory design
Extensive experience in 3D modelling and digital design (preferably with Autodesk tools)
Extensive experience in software engineering and software development software quality control
Extensive project delivery experience including the timely delivery of relevant output.
Demonstrable evidence of developing and executing substantial research projects.
Ambition and passion to deliver commercial outcome from generated IP.
Skills to attract future research funding
An entrepreneurial spirit
Excellent networking, communication and interpersonal skills.
The ability to lead a highly focused and academic team.
Flexible with a proactive approach.
Ability to work under pressure and meet

Skills/Experience Preferred
Financial Acumen

Education Required
A PhD or extensive and nationally recognized

Caresoft Global Limited operates as an Employment Business and Employment Agency.
We are an independent highly-experienced recruitment consultancy dedicated to specialist markets within the Automotive, Aerospace, Agricultural&Construction Industries.

No terminology within this advert is intended to unlawfully discriminate on the grounds of age, sex, race or disability and we welcome all applications
1015387| MWWS| Hadoop Developer (Perm or Contract)| Hadoop Developer (Perm or Contract)

Job Location: New York, NY

Job Description: As part of the product development team and reporting into the head of engineering Hadoop Developers will help develop scalable ELT/ETL workflows to transform and integrate data in to structures conducive for reporting and analytics on top of Teradata warehouses for one of the largest globally financial services companies. You will design and implement dimensional data models that scale across multiple data warehouses that will feed into Hadoop to replicate data from the Teradata databases. Using tools such as Sqoop, Impala, or Teradata ETL you will load huge volumes of data from Teradata into Hadoop cluster. You will then use Map/Reduce, Hive, Pig to process/analyze it and export aggregates back into Teradata for reporting.

Responsibilities:
We are looking for seasoned developers who thrive in a start-up environment. Qualified candidates are seasoned ETL and Tools developers who are accustomed to working across large independent databases and massive amounts of data. The Tools / ETL Developer will function as data expert to advise business analysts in the usage of structured and unstructured data.

Requirements:
• Experience developing Develop, implementing, and refining data engineering solutions for huge volumes of data.
• Professional experience with Hadoop, Map/Reduce, Pig/Hive/Impala, Sqoop etc.
• Data Warehouse experience with Teradata, Oracle etc.
• Experience designing and implementing dimensional data models that scale across an enterprise business.
• Experience building scalable ELT/ETL workflows to transform and integrate data in to structures conducive for reporting and analytics in Hadoop.
• Familiarity and experience in different phases of software development life cycle.
• Good understanding of algorithms, data structures, performance optimization techniques, and object-oriented programming
• Excellent communication, interpersonal, and problem-solving skills
• BS in Computer Science or equivalent
• MS or PhD in Computer Science
• Professional experience of ETL

Salary $100k to $130k
1015519| Axess Ltd| Middlesex, Surrey, Berkshire, Buckinghamshire, London| Benefits:

Car allowance + corporate package

JOB SUMMARY

This is a high profile publications role for this leading, rapidly growing pharmaceutical company. You will lead the development and execution of globally aligned strategic publication plans across the Urology portfolio, lead English publication activities in the product publication plan globally for all marketed products and compounds in post-POC clinical development

BACKGROUND

Reports to the Senior Director of Scientific Publications
This role requires working with a global team and may involve up to 10% travel
Medium pharmaceutical company - exciting pipeline.
Excellent benefits

PRIMARY DUTIES

* Engages Director&Senior Director leaders across the organisation's global medical community in the translation of medical strategies&objectives into actionable strategic publication plans
* Evolves strategic publication plans in line with clinical development milestones and changes in the scientific, regulatory and access landscapes globally and in key markets
* Gains endorsement strategic publication plans (Annual Publication Plans per product) by governance bodies per company policy and SOPs prior to execution
* Demonstrates understanding of disease area, medical strategies&objectives required to provide strategic input to leaders on matters related to publication planning&data disclosure
* Implements effective&consistent strategies for engaging external expertise (e.g. Publication Steering Committees) to advise on&shape strategic publication plans
* Fosters collaborative relationships with academic&clinical experts, publishers, medical associations&other relevant stakeholder groups
* Leads the execution of the publication platform across the portfolio (abstracts, presentations) at prioritized International&Regional congresses
* Reviews publication drafts for scientific quality and to ensure alignment&consistency with author direction, scientific communication platform&key communication points supported by data
* Facilitates decision making during publication planning&execution process through effective alignment across a broad range key internal stakeholders (CMTs, GDPTs, Health Outcomes&Alliance stakeholders)
* Accountable for meeting budget objectives, projects goals within department priorities

QUALIFICATIONS / EXPERIENCE REQUIRED:

Required Experience:
* Advanced Degree in a scientific or medical discipline (PharmD, PhD, MD) required
* Advanced level experience in the healthcare industry with significant expertise across all aspects of scientific publication strategy, planning and execution
* Past scientific expertise in urology
* Demonstrated track record of executing in highly matrix environment working across wide range of functional areas Medical Affairs (Global and Regional), Health Outcomes, R&D, regulatory, legal and commercial teams
* Understanding of clinical trial design and execution, statistical methods and clinical trial data reporting requirements
* Understanding of good publication practices and guidelines, Sunshine Act, IFPMA and Pharma Code of Conduct, ICMJE, GPP2, and other guidelines related to publications and scientific data communication
* Outstanding interpersonal, written and verbal communication skills with exceptional time management skills are required for this highly visible global position
* Ability to function effectively on a strategic as well as tactical basis
* Demonstrated track record of managing multiple priorities with successful outcomes
* Demonstrated track record of experience in medical writing, editing, and review
* Working knowledge and familiarity with publication management tools&systems
Preferred Experience:
* Doctoral degree or equivalent, with preference for M.D. or Ph.D.
* Experience managing publications in a global environment
* Medical writing experience

TO APPLY:

For a confidential discussion please telephone (Julia Day) at AXESS Limited on . To apply, please click above quoting reference EM 6181

Keyword: medical communications, medical comms, medical publications, publications management, publications director, Associate Director, Product Publication Lead, GPP2, urology, transplantation, Berkshire, reading, Slough, High Wycombe, ascot, Bracknell, Windsor, maidenhead, Basingstoke, Henley-on-Thames, medical communications.

ABOUT AXESS:

AXESS has been operating since 1990
We are a recruitment business dedicated to the pharmaceutical industry, specialising in Medical Affairs, Regulatory Affairs&Clinical Development
We match professional candidates to the best permanent, contract and interim roles in the market
1014683| Cummins| Product Design Technical Specialist (Electromagnetic)| Product Design Technical Specialist (Electromagnetic), Peterborough, UK or Craiova, Romania

Company overview
Cummins Inc., a global power leader, is a corporation of complementary business units that design, manufacture, distribute and service engines and related technologies, including fuel systems, controls, air handling, filtration, emission solutions and electrical power generation systems. Headquartered in Columbus, Indiana, (USA) Cummins employs approximately 48,000 people worldwide and serves customers in approximately 190 countries and territories through a network of more than 600 company-owned and independent distributor locations and approximately 6,500 dealer locations.

Peterborough
At Cummins Generator Technologies, it's not just the products we make that set us apart - it's how we engage our customers every day. The unique combination of knowledge, dependability and innovation we bring to each customer relationship turns everyday service into excellent customer support. As a result we help our customers operate with greater efficiency, making it possible for them to compete more successfully throughout the world. Key functions of our business moved to our new facility in Peterborough late 2013.

The Opportunity
As the Product Design Technical Specialist (Electromagnetics), you will be "the specialist" the Engineering team look to for ideas, inspiration and ideas to develop our next generation products.

Key Responsibilities not limited to:
* Applies highly specialized knowledge of engineering principles and practices to assigned areas and projects in the design, development, analysis and release of products
* Verifies design using analysis and or functional testing, interprets results, drives decisions and assesses risk
* Works with other engineering disciplines and cross-functional disciplines to resolve product issues. Evaluates customer needs and aligns requirements with identified customer expectations
* Fill the role of an assistant chief engineer, product readiness leader or project engineering leader
Leads large or multiple engineering projects
* Performs as the local technical expert for one or more engineering specialties
* Solves complex problems impacting multiple projects
* Communicates with and influences key external stakeholders and business leaders
* Drives and manages system level requirements for projects or programs
* Makes critical program-related decisions
* Collaborates with industry peers within their discipline
* Advances the state of the practice for the technical discipline
* Sets strategic direction for a program or technical discipline
* Advises and transfers knowledge, coaches and mentors less experienced engineers
* Advises leaders for resolution of complex business problems

Skills and Experience
* Can translate relevant codes and standards into product requirements
* Is aware of technology trends in industry and can support and suggest future product development
* Can define relevant Engineering standards and design guides
* Can apply advanced electromagnetic engineering principles
* Can optimise electromagnetic product performance, including reactance, efficiency, motor starting capability
* Can define and optimise excitation systems for synchronous alternators including exciter, Automatic Voltage Regulation and Auxiliary winding, permanent magnetic generator excitation
* Understanding of the fundamental principles of insulation systems, thermal management, and mechanical design of synchronous alternators
* Substantial relevant work experience required, including leadership of small projects or portions of large projects
Preferably experience of engineering synchronous alternators

Education, Licenses, Certifications
PhD, Masters of Science, Bachelor of Science or equivalent degree in engineering required.

What's on offer?
In return, as Product Design Technical Specialist you can look forward to a secure and rewarding future with an acknowledged market leader, able to offer a competitive compensation C£60,000 with bonus which includes a base £43,000-54,000K, variable bonus 12%, and benefits package and genuine prospects.
1016333| EMD| QPD NBE Outsourcing Manager| EMD Serono is the biopharmaceutical division of Merck KGaA, Darmstadt, Germany, a global pharmaceutical and chemical group. We strive to create value and benefit patients by transforming medical science into breakthrough solutions in our core therapeutic areas of neurodegenerative diseases, fertility and metabolic endocrinology, as well as oncology and autoimmune/inflammatory diseases as emerging areas of expertise.

PURPOSE OF THE ROLE
QPD NBE (New Biological Entity) Outsourcing Manager is a scientific and operational role within Quantitative Pharmacology and Drug Disposition (QPD), responsible for outsourcing of clinical drug disposition contribution to NBE projects, to fulfill internal and regulatory requirements. Furthermore as collaboration manager she/he is accountable to efficiently manage CROs for given projects and to deliver validated clinical bioanalytical and immunogenicity assays&data.

KEY TASKS AND RESPONSIBILITIES
•Clinical NBE bioanalytics
â-¦In collaboration with the preclinical NBE bioanalytical organization, develop and deliver the clinical bioanalytical strategy, ensuring consistency with the preclinical bioanalytical strategy and taking the biology and the quantitative pharmacology strategy into consideration
â-¦Accountable that outsourced clinical bio analytical and immunogenicity activities are performed according to the agreed timelines and quality and in compliance with current guidelines and internal standards
â-¦Acts as senior expert supporting clinical immunogenicity and bioanalytical testing at CROs and ensures that studies are performed according to the agreed standards and costs.
â-¦
â-¦In her/his roles as collaboration manager towards CROs she/he conceives, implements and updates the clinical bioanalytical plan for given projects, in line with QPD/PR requirements, revising this strategy on an agreed basis
â-¦Maintains a robust and effective relationship with preferred partner CROs in given projects and manages any issues to an effective resolution.
â-¦Ensures that preclinical pharmacokinetics / immunogenicity testing/ clinical bio analytics issues are discussed, also dependent on the stage of the molecule, appropriately within the function
â-¦Oversees the budget for outsourced/internal studies related to drug disposition
â-¦Ensures that the appropriate budget and resources are allocated in iMAP for development projects
â-¦Tracks costs related to discovery studies performed internally or externally

•Additional role :
â-¦May assume the role of QPD PR, representing the QPD function as core team member in development projects
â-¦May provide exploratory PK evaluations
â-¦May provide drug disposition expertise for external opportunity evaluations
CANDIDATE'S PROFILE
•Master or PhD degree in chemical-biological-pharmaceutical field
•Several years of professional experience (>4 years) in the field of bioanalytics for biologics (NBE)
•Several years of experience in leading an NBE bioanalytical team
•Good understanding of drug development&discovery processes
•Working experience in GxP regulated environment
•Excellent scientific understanding DMPK and immunogenicity related matters
•Excellent knowledge of NBE work packages (non-clinical and clinical)
•General knowledge of disease area, more in depth understanding of biology, pharmacology
•Excellent knowledge of regulatory requirements
•Good understanding about translational sciences
•Proficient in communication with impact
•Proven managerial skills
•Excellent self-organization
•Fluent spoken and written English
•Good intercultural understanding
•Strong mature leadership and influencing skills

Equal Employment Opportunity
The Company is an Equal Employment Opportunity employer.
No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, or any other classification protected by applicable federal, state, or local law.
This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment.
Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to his/her Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because he/she made a good faith report of discrimination.

Company Description:

EMD is the North America name of Merck KGaA, Darmstadt Germany. We are a global pharma and chemical company. In the United States we are mainly operating under the brands EMD Millipore and EMD Serono.

With more than 300 years of progress and over 38,000 employees, we are leading in pharma and chemicals. With passion, dedication and innovative ideas, we pursue one global goal: to improve people's quality of life.

Like to join in? Welcome to the team!

1017570| IT Connections Ltd| C++ Software Engineer / Graphics Programmer / Open GL| Position: C++ Software Engineer / Graphics Programmer / Open GL
Newcastle, Gateshead, Durham
£25,000 to £35,000
C++ Software Engineer / Graphics Programmer / Open GL required to join team working on cutting edge real time virtual environment rendering engine. This role would suit a C++ Software Engineer with a placement year or 1 / 2 years of commercial experience in a software development team. You should have a Computer Science, Maths, Physics or Games Programming degree (candidates with MSc or PhD will also be considered) and ideally a Maths A- Level or equivalent. You should have strong programming skills (multithreading) in C++ and or C# and knowledge of tools such as Open GL, Direct X, HLSL, and the Unity game and rendering engine. This C++ Software Engineer role will join a team working at the forefront of 3D technology for blue chip clients, and you will be working with high end hardware - graphics cards, high spec PCs, to produce award winning data visualisation and 3D visual effects software. Excellent technical communication skills are essential, you will join a highly skilled team of working on leading products in a fast growing and forward thinking company. This is a great opportunity for a skilled and ambitious C++ Software Engineer with an interest in 3D graphics programming to build their career and work on really exciting projects. C++ Software Engineer / Graphics Programmer / Open GL
1017381| Aspire Data Recruitment| Lead Analyst - Risk Model Validation| Job Title: Lead Analyst - Risk Model Validation
Location: Leeds
Salary: to £50,000 + bonus&benefits

Reporting in to the IRB Modelling Manager, you will support the development, maintenance and implementation of IRB models by proactively identifying risk modelling issues and leading analytical projects to address these through a combination of advanced data mining, advanced statistical analytics and credit risk model development.

Candidate Profile

- Educated to at least degree level (minimum 2:1) with an emphasis on mathematical / analytical techniques. Masters and/or PHD preferred
- Experience of working in credit risk (or similar), within a financial services organisation, including expert knowledge of at least one of (or comparable experience in a similar field): Credit risk model development, Portfolio analytics, Advanced IRB ...
- Have expert skills in data manipulation, SAS (or similar statistical packages), SQL and Microsoft Excel. SAS Certification desirable
- Have outstanding analytical and problem solving skills
- Have the ability to coach and develop junior colleagues
- Have proven ability to take a lead role in analytical projects

Please send your CV to Email address removed 1 or call us on Phone number removed

Links:
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1 mailto:Email address removed
1014886| Memory Training Centers of America| Psychologist - Newly Licensed| Company Description:

MTCA currently operates in ten States with development in progress nationwide.
For more information about MTCA, please visit:

Job Description:

Memory Training Centers of America (MTCA) is the leading provider of cognitive evaluation and treatment services to older adults. We work with individuals residing in assisted living communities who suffer memory loss. With over 40 years of experience in working with cognitive disorders, Dr. Magaro (Founder/CEO) has developed a proprietary treatment program, to diagnose and treat older adults suffering from memory loss.

Since our inception in 2001, communities that have embraced MTCA services are already reporting significant improvements in the quality of life of their residents. So far, the demand for these services cannot be fully met due to the shortage of contract clinicians in our network.

MTCA is actively seeking for a number of contract Psychologists to meet our client needs. The ideal individual(s) will be required to deliver all the following:

Willing to travel to facilities to provide care to the residents
Completed accredited PhD or PsyD program
Licensed by the Board of Psychology as a Clinical Psychologist in the state practicing
Must be able to meet the requirements of MTCA Credentialing Department
Prior geriatric experience preferred and interest in working with this population
1017234| RBW Consulting Solutions Ltd| Statistician II, UK| * Statistician II and Senior Statistician role with what has grown to be a global CRO with an increasingly excellent industry reputation
* Work across programmes and portfolios of an assortment of high profile sponsors as well as more specialist, lesser known companies
* Field based, UK
* Excellent international support network
* Up to £45,000 + benefits

Two Biostatistical professionals are required by a growing global CRO in the UK (one Statistician II and another Senior Statistician). The successful applicant will contribute to and, dependant on experience, in some cases lead the design, analysis, and reporting of clinical studies. Depending on experience, they will provide statistical leadership across programmes and portfolios of studies for an assortment of high profile sponsors. For the more senior, they will act as a Subject Matter Expert and take the lead in departmental initiatives helping to further grow the team.

Applicants should be able to communicate technical statistical information to a non statistics audience, have a BSc or ideally an MSc or PhD in Mathematically related discipline and have the desire to work for a company that recognizes and rewards individual merit.

Should this position in not initially seem 100% suitable, do still get in touch. I work with a variety of other Biotech companies, Pharmas and CROs across the EU and I'd be pleased to speak with you about your options in general. Call (O) or email .com for a confidential discussion about your options.

Keywords
Pharmaceutical, CRO, Biotechnology, Biostatistics, Biometrics, Statistics, Principal Statistician, Senior Statistician, Lead Statistician, SAS Programming, R, Statistician, SAS, Clinical Trials, Regulatory Affairs, EMEA, Statistician, ICH, FDA, Submission, Europe, Pharmaceutical, Biotechnology, Biostatistics, Biometrics, Statistics, Statistician, Principal Statistician, Senior Statistician, Lead Statistician, SAS Programming, Clinical Trials, Regulatory Affairs, Statistician, Submission, Europe, Pharma, Statistician
1017422| Bluebolt Recruitment Limited| Polymer Sales Manager - SE and Midlands| We are seeking a Sales Manager to work for a polymers manufacturer. The position is a home and field based role covering SE England and the Midlands - including Derbyshire, Nottinghamshire, Lincolnshire, Warwickshire, Oxfordshire, Surrey and West Sussex.

The basic salary is £28,894 + at least £6,000 bonus + company car.

The company is undergoing rapid growth which is based upon an excellent product development strategy and wishes to recruit a Sales Manager to sell its technically advanced adhesives and coatings. Applicants, who will be graduates with a 2:1 Science based degree preferably in Chemistry/Material Science (Polymers), must be able to demonstrate the ability to successfully sell technically advanced products to industrial users through
customer trials/ demonstrations, and operate effectively at all levels within the customers' structure. They are also required to provide technical support to the existing customer base. A background of selling formulated chemical systems would be a distinct advantage or a candidate with experience in a technical role with some customer support who is now looking to move into technical sales. The customers are industrial users/ installers of polyurethane products.

key words : Chemical sales manager chemical sales representative polymer sales manager polymer chemistry polymer science polymer engineer graduate chemist polymerisation biocompatible and polyester copolymer Polymerisation polylactide process chemist process chemistry scale up scale-up technical transfer process technologist pharmaceutical technologist process scientist manufacturing chemist manufacturing scientist production chemist production scientist process development chemist process development scientist pilot plant pilot-plant synthesis synthesize synthesise synthetic ganic ganic synthetic ganic chemist ganic chemistry synthetic chemist synthetic chemistry synthetic scientist polymer polymer monomer bsc chemistry msc chemistry phd chemistry degree in chemistry chemistry chemist material science materials science
1017093| Intergen Group| Project Manager- Infrastructure Project| Company Description:

Intergen, LLC a specialty technology consulting services firm. Intergen offers a cost-effective consulting approach to satisfy an array of software engineering and IT solutions, including web application&portal development, mobile platform development, telephony engineering, PLM/PDM, software quality and testing.

Job Description:

Below is a technology summary:

Citrix
Cisco UCS implementation
VMware
VMax
AIX
Wintel

Unique Skills:
Education and Experience Requirements:
Bachelors in CS, IS, related field, or equivalent combination of appropriate education and/or experience. Masters in Management or related field preferred.7+ yrs in an IT/IS environment. Extensive project management experience, Certified Project Manager (CPM) status and/or Project Management Professional (PMP) certification preferred. See Other Requirements in Job Description.

Position Purpose:
Plans, executes, and finalizes projects according to strict deadlines and within budget. The Project Manager is responsible for defining the projects objectives and providing day-to-day coordination to ensure quality control throughout the projects life cycle.

Principal Duties and Responsibilities:

Essential Functions: 1. Develops individual group project plans (project work scope, task descriptions, budget estimates and manpower requirements) to meet objectives and commitments. 2. Develops, maintains, and monitors master project schedule. 3. Defines and implements project standards and processes for structuring all IT projects, including process/documentation evaluation and improvement. 4. Tracks projected vs actual project performance and informs management of accomplishments and major problem areas as well as budget&schedule status. 5. Develops and executes enterprise-wide communication plan as related to milestones via status reports, and presentations suitable for all levels of management and staff. 6. Conducts post implementation project reviews to evaluate sustaining support and document lessons learned.

Additional Functions: 1. Develops project documents through work with business analyst, technical and customer contacts. 2. Maintains current knowledge of technical and process developments in the project management arena. 3. Maintains and analyzes project budget. 4. Performs other duties as assigned.

Other Requirements: 1. Experienced in managing and monitoring the work of team members and ability to provide project leadership and training. 2. Demonstrated knowledge of accepted Project Management principles and practices. 3. Excellent analytical skills with special attention to detail. 4. Ability to lead/facilitate cross-functional teams and meetings. 5. Ability to meet tight deadlines. 6. Ability to work in a highly dynamic environment. 7. Ability to successfully build teams and foster an atmosphere of collaboration. 8. Strong interpersonal skills. Ability to work well with managers, directors, a diverse department, and a variety of internal and external customers. 9. Works to resolve resource constraints by leveling resources in project planning activities. 10. Works to secure funding from project sponsors for unbudgeted efforts. 11. Identifies/escalates issues as necessary. 12. Excellent written and verbal communication skills. 13. Excellent presentation design and delivery skills. 14. A Masters degree may be used to offset one year of experience; PhD may offset two years of experience.
1017069| Canon| Intern - Research| Position Overview:
Research Interns (Computational Imaging Group)
The Canon USA Innovation Center located in San Jose, CA is seeking graduate students (MSc/MEng/PhD) for internships in 2015.

Responsibilities:
Work on research topics related to image capture and analysis within computational photography, computer vision, and large-scale analysis.

Qualifications:
Qualifications:
• Ph.D. student in Engineering and/or Computer Science
• Knowledge of Matlab, C/C++, Python
• Research background in one or more of the following:
- large-scale image/data analytics
- computer vision using machine learning techniques
- computational imaging
- 3D reconstruction
- simulation of imaging systems
• Good written and oral communication skills
1017581| PHD Technology Solutions, LLC.| 3rd Shift Controls Engineer / PLC Programmer| Company Description:

PHD Technology Solutions, LLC is proud to be an equal opportunity employer and employees or applicants will receive consideration for employment without regard to age, color, disability, gender, national origin, race, religion, sexual orientation, protected veteran status, or any other classification protected by federal, state, or local law. The preceding position description is intended to provide the general nature and level of work to be performed by employee. It is not intended to be a detailed description of the position or a comprehensive listing of all duties, responsibilities, and qualifications required of employees assigned to this position.

Job Description:

PLC Programming, manage assigned projects and duties
Controls experience in RSLogix5000, RSLogix500, RSLogix5, FactoryTalk View Studio ME and SE, GE Proficy Machine Edition, Siemens Step 7, Siemens WinCC, Other PLCs and HMI, Wonderware.
Assist in troubleshooting and repair of electrical problems as required
Perform continuous improvement activities to improve safety, to increase productivity and to reduce production cost, by development and improvement of electrical control systems, PLC, HMI&robotics programming including design, implementation and troubleshooting
75K Salary + Incentives
1014045| Anchor Staffing Inc.| Clinical Care Manager (LMFT, LCPC, LCSW, PhD)| Company Description:

See our company profile at

Job Description:

Position Summary&Specifications

Clinical Care Managers are Licensed Clinical Social Workers, PhD Clinical Psychologists, Licensed Clinical Professional Counselors or Licensed Marriage and Family Therapists in the State of Illinois wanting to join an innovative team of professionals as part of the Illinois Mental Health Collaborative for Access and Choice (The Collaborative). The Collaborative is a partnership between the Illinois Department of Human Services/Division of Mental Health (DHS/DMH) and ValueOptions with Anchor Staffing, Inc. The ideal candidate will be comfortable in a call center environment, performing telephonic assessments, collecting sufficient data to make appropriate referrals, and determining if appropriate levels of care are being provided. Will collaborate and coordinate with providers, consumers, and the treatment team to evaluate clinical appropriateness of treatment and interventions. Works with providers and facilities to monitor and evaluate care at regular intervals to ensure that treatment is designed to meet the Consumer's individual needs and that progress is being made towards the consumer's goals. Uses approved clinical policies, procedures, and clinical criteria to provide administrative services within benefits.

Qualified professionals will perform the following essential duties and responsibilities:

Responsible for clinical decisions related to assessment, referral, coordination of care, and appropriateness of care for consumers seeking access to their benefits for Mental Health or Substance Abuse services for all levels of care covered by contracts, using established criteria, guidelines, and policies.
Responsible for triage and management of emergency calls.
Responsible for meeting standards related to clinical documentation, clinical policies and procedures, accreditation and regulatory standards, and contract compliance.
Actively participates in clinical rounds/case review process, and seeks consultation with the Clinical Director and Medical Director as needed.
Actively participates in the designated processes to manage the care of high risk consumers.
When necessary, responsible for clinical oversight of activities performed by non-licensed staff members.
Maintains confidentiality and ethical and professional standards. Performs other duties as assigned.

Applicants must possess the following minimum qualifications:

Education: Commensurate with License.
Licenses: Must have a current, valid, unrestricted license as a LCPC, LCSW, PhD Clinical Psychologist, or LMFT in the State of Illinois.
Relevant Work Experience: Must have 1-3 years post-licensure direct practice experience. Prefer 1-3 years of managed care experience.

Ideal candidates will need job specific skills including:

Strong customer service orientation.
Excellent written and verbal communication skills
Knowledge of treatment resources and levels of care available.
Ability to function in an interdisciplinary setting.
Able to engage with providers in positive shaping strategies.
Must be proficient in applicable Microsoft applications, Internet Explorer, and have the ability to learn additional proprietary software.

Access to Confidential Information

Adheres to all policies on confidentiality as defined by HIPAA.

Qualified candidates should email their cover letter and resume to:
1016515| Opus Resourcing Ltd| Software Engineer - Network Modelling / Analytics - Blue Chip| Software Engineer with strong programming skills in Python, Perl, Matlab, Ruby or R Programming skills combined with Database skills such as MYSQL, or Oracle etc and strong academic background with Masters or PHD in Computer Science or telecoms and an insight into network protocols is required by blue chip technology giant in the City of London. Any experience of network modelling tools such as OPNET, Cariden or NS2 would also be an advantage.

Key elements of the role will include

Responsibilities include:
*Data Gathering and Network Visualisation
oDevelop and support the middleware between OSS services and the I&P database infrastructure
oDevelop and maintain tools to automatically generate reports and graphs illustrating network topology, network performance and healthiness
*Software Development
oDevelop software using popular web frameworks to support interaction with delivery teams
*Network Planning
oApply data science methodologies to develop traffic forecasts
oDevelop current and planned network topology models
oAvailability planning based upon failure simulations
oCost modelling and evaluation
*Network Improvement Analytics
oData science methodologies to analyse and improve broadband Quality of Experience
*Business Intelligence Analytics
oInsight analytics to support commercial/BI objectives

This is an outstanding chance to flex your technical and analytical skills for a world leading technology company.

Opus Resourcing acts as an employment agency in respect of permanent employment.

1017293| Helix Recruitment Ltd| International Product Manager - Flow Cytometry - Birmingham| ROLE
As International Product Manager for Clinical Flow Cytometry you will be responsible for the promotion of Flow Cytometry Reagents into NHS Hospitals / Clinical Laboratories in line with the company's Sales Strategy and Marketing Plan. Working for this global organisation, your role is both strategic and "hands-on", with the opportunity for you to shape and evolve the marketing department. Working from the company's state of the art offices in Birmingham you will have a high degree of autonomy and the ability to conceive, plan and execute a Global Sales and Marketing Strategies whilst delivering results at pace.

Core responsibilities as International Product Manager - Clinical Flow Cytometry :

* Monitor sales vs. target providing proposals for marketing initiatives for continued sales growth
* Creation of promotional literature
* Liaison with Technical Service Department for on-market support, surveillance and complaints
* Work closely with Scientific Affairs Managers to ensure scientific activities with customers and KOL's are in line with the company's sales and marketing plans
* Involvement in UK and International e/mailing, ad campaigns and other promotional campaigns as well as manage the process with the Marketing communications group
* Management of marketing requirements of New Product Development System including market research, forecasting and commercial justification
* Work closely with global and country Advertising and Promotions teams during launch phase to ensure successful product launches
* Post launch product cycle management with guidance from global and country Marketing departments
* Develop and deliver training modules for sales, application specialists and distributors' as well as regularly review and update training materials and marketing collateral content
* Awareness of market requirements and competitor products and proposals for counter competitive initiatives
* Attend international exhibitions and meetings related to clinical Flow Cytometry

COMPANY
This UK based company is a market leader in the development of immunology products for the investigation of a range of disorders, and sold worldwide through their own subsidiaries and network of distributors. They offer first class products to their customers, and superb training, support and development to their employees. The company actively promotes from within so there are genuine opportunities to progress your career once you've proven yourself.

REQUIREMENTS
In order to apply you should meet all or most of the following criteria:

* MSc or PhD in a life science subject
* Practical experience within the field of immunology and / or haematology
* Experience of product management and launch for Flow Cytometry products, particularly clinical Flow Cytometry
* Proficient in developing successful new strategies to tackle complex issues or difficult competitive situations such as customer conversions from 4-6 colours systems to 8-10 colour systems and competitor reagent rental agreements.
* Experience of developing new markets and launching Flow Cytometer Systems
* International experience coupled with the success of achieving sales targets
* Must be able to travel internationally

Living in the United Kingdom and happy to travel internationally, you should be living in or within a commutable distance of any of the locations: West Midlands, Wolverhampton, Coventry, Dudley, Solihull, Sutton Coldfield, Walsall, Birmingham, West Bromwich, Stourbridge,

REMUNERATION
Package includes:
Basic salary of £50,000, depending on experience, plus bonus
Car allowance of £500 per month
Benefits include: - pension (6%), private healthcare, life assurance, 24 days holiday
Genuine opportunity for career development

KEYWORDS
Product Manager, Sales, International Sales, Marketing, Flow Cytometry, Reagents, Instrumentation, Birmingham, Immunology, Haematology, In-Vitro Diagnostics, Product Management, New Product Development, Clinical Flow Cytometry, West Midlands, Wolverhampton, Coventry, Dudley, Solihull, Sutton Coldfield, Walsall
1017159| CLF Staffing| Wintel System Engineer| Public Trust clearance (SRF 1289)

Job Description:

Windows systems engineer/administrator with data center experience supporting Windows 2003 and 2008 installation, operations and maintenance; VMWare; Citrix XenApp; Bladelogic/Shavlik.

Responsible for driving technical service resolution and maintaining high levels of customer satisfaction through pre- and post-engineering technical/functional support to current and prospective customers. This position is responsible for providing systems engineering support for customers in a 24x7 service organization.
Acts as a lead customer issue resolution engineer and takes ownership of all assigned tickets.
Acts as a mentor to other engineers, as assigned, and to develop internal certification criteria and curriculum.
Acts as a subject matter expert for the disciplines outlined below in job requirements
Perform the duties of Level 2 Engineers, Training Coordinator, QA Engineer and Escalations Manager as assigned and certified.
Participate on rotating shift coverage's, as needed to support organizational goals; Participate in the company on call program, as needed to support organizational goals.
Coordinates with client management to formulate highly complex technical solutions. Identifies and implements solutions based on client needs. Informs client management of appropriate developments in technical support products.
Provides technical leadership to internal and external personnel on highly complex system installation and administration activities. Provides technical solutions and escalated support for non-routine, highly complex technical issues. Mentors and provides guidance to less experienced personnel.
Evaluates products and upgrades for appropriateness of cost and compatibility. Oversees and implements system upgrade strategies.
Develops and analyzes highly complex system standards, thresholds, and recommendations to maximize system performance. Initiates reviews as appropriate.
Conducts capacity planning reviews with management and approves capacity plans formulated by less experienced personnel.
Develops strategies to manage the frequency of appropriate support package/patch application. Monitors database maintenance and provides appropriate recommendations, when required. Implements solutions and refines procedures as appropriate.
Coordinates with business development personnel on proposals and work estimates involving highly complex system administration projects and solutions.
Researches current systems technology and serves as subject matter expert on complex systems processes and procedures. Conducts usability and costing studies.
Industry certification (CompTIA, MCSE, MSITP, ITIL, etc..)
Experience with Windows 2003 - 2008 Server, Exchange Server, Active Directory, Group Policies, Patch management, Log management, WSUS, SCOM, VMWare

Qualifications

Contract qualifications: Bachelors Degree from an accredited college or university with five years of related experience. Equivalents: HS diploma with nine years of specialized experience, or Associates Degree with seven years of experience, Masters with 3, PHD +1

Basic Qualifications

Bachelor's degree or equivalent combination of education and experience
Bachelor's degree in systems engineering, computer science, management information systems, or related field preferred
Four or more years of experience in systems engineering, software engineering, operating systems programming, or naval architecture.
Experience working with computer hardware, operating system software and desktop applications with a specific concentration in one or more areas
Experience working with one or more structured programming languages
Experience working with design principles and applications

Other Qualifications

Analytical and creative problem solving skills for design, creation and testing of systems
Communication skills to communicate system proposals to management and customers and provide systems diagnoses and resolution for current systems
Interpersonal skills to interact with customers, senior level personnel, and team members
Organization skills to balance and prioritize work
Leadership skills to assist less experienced personnel
Ability to integrate moderately complex hardware and software systems
Ability to work independently and as part of a team

REQ# C144
1016631| Michael Bailey Associates - Eindhoven| Process Investigator|

Process Investigator

Duration: indication 1 year

Startdate: 1 April 2015

Interviews: as of week 10

Location: Venlo

Introduction: The Consumables and Processes (C&P) department is part of the Research and Development organization in Venlo with approximately 800 employees in total. C&P assures the development of competitive products by realizing the involved print (imaging) processes with the right print quality and reliability. C&P is also continuously working to enlarge the application range of the printer technology and to take care of development and engineering of the strategic consumables, like toner. At this very moment part of the program is to optimize and improve toners for the electrophotographic digital printers. For this we need new physicists.

Position's main tasks: As a physicist you will be, at our research and development facility in Venlo, part of a multi-disciplinary team, consisting of physicists and chemists. In this multi-disciplinary environment you will be the intermediate person who has to be aware and to deal with the complex interactions between the several printer functions. A fully understanding of the applied test methods and applied physics is part of the job. You are responsible for organizing, setting up and implementation of an appropriate test program. At the end you have to prove the feasibility of these new toner formulations for the current and new printers. You will report and discuss your results and solutions in your development team. Within this dynamic position, in a multiple stakeholder dialogue, you can extend your skills and knowledge beyond your own craftsmanship.

Need to have: Master or PhD in Physics

Communicative, team player, hands on mentality. You are looking for a job where you can combine physics and material testing. You are pragmatic and result-oriented. With your independent attitude and enthusiasm you bring topics up for discussion, and convince others with your ideas

Michael Bailey International is acting as an Employment Business in relation to this vacancy.

1015703| The Judge Group| Psychologist| Company Description:

Founded in 1970 by Martin E. Judge Jr., The Judge Group is a professional services firm offering Technology Consulting, Enterprise-Wide Staffing and Corporate Training.

The Judge Group has long believed in strong companies and the talented people who help them grow. Forty years of experience have taught us how to best address the cultural and economic needs of our clients, expertly assist candidates in navigating through their own unique career progressions, and create, maintain, and nurture valued community partnerships.

Job Description:

Psychologist needed ASAP!

Clinton MA!

Up to $83,000!

Our client is located in the Clinton Mass and surrounding areas is seeking a licensed Psychologist who has a passion for treating older adults and providing the highest quality care in nursing homes and assisted living facilities. You will be part of a collaborative team that includes psychiatrists, nurse practitioners, and clinical social workers. Although you work fairly independently, you have the support of your clinical supervisor, peers and office staff.

Our Psychologist plays a vital role in the effective treatment of symptoms and behaviors associated with dementia and psychiatric disorders. There are traditional nursing homes and assisted living facilities, facilities that have a higher acute psychiatric population, and ones that care primarily for veterans and others who have a variety of residents in both age and diagnosis.

You be provided mileage reimbursement.

Qualifications:

You will play a vital role in the effective treatment of symptoms and behaviors associated with dementia and psychiatric disorders.
You will perform initial evaluations, neuro-cognitive rehab therapy, innovative behavioral management, traditional psychotherapy and milieu treatment.
You will participate in our Mental Health Rehabilitation Program which is designed to provide maximum support to rehab patients who are receiving PT, OT, and/or SLP therapy in skilled nursing and assisted living facilities.
You will set standards of care for dementia and behavioral health services in long-term care and sub-acute rehab facilities.

Requirements:

Have a doctorate degree in psychology: PhD, PsyD or EdD.

Have an unrestricted state license as a licensed psychologist or in the process of obtaining this.

Prior geriatric experience is preferred.

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