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laboratory manager in Raleigh

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  1. Lead Systems Analyst,Clinical Orders-pd relo to Hartford, CT-bzs4171

    The Lead Systems Analyst is responsible for designing, implementing, and maintaining the organizations enterprise Electronic Medical Record system.  The focus areas for this role are CPOE, Closed-Loop Medication, Patient Lists, Orders/Results Viewing, and Clinical documentation.  Desired candidates will have experience with Epic, Laboratory System integration, and Certification in Nursing, Clinical Informatics, or Project Management Professional.   Acts as a team leader for the Epic EMR, providing ...

  2. Engineering Technology Director

    Purpose: This document contains the job description information for the job position Technology Director. Scope: This document provides general information about the job position, identifies the basic skills and competencies required for the position, and identifies general hazards and safety considerations that are associated with the position. Additional specific information about this position is included in the company policies, procedures, and work instructions that apply to the situations ...

  3. Validation Engineer

      Here at ProPharma Group, we work with clients in the pharmaceutical, biotechnology and medical device industries to provide the best solutions for their unique challenges and concerns. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes. Our goal is to provide the information our clients need to deliver safe, effective and quality products and services every time. Responsibilities: A Validation Engineer at ProPharma ...

  4. Scientist (virology)

      Scientist  Morrisville NC 27560 6 month contract Pay rate: $26-$30/HR   Specific Duties, Activities, and Responsibilities Develop and execute laboratory work plans/schedules independently, using customer milestones and Division/site performance standards and metrics Authors technical documents, such as protocols, test methods, text reports, certificates of analysis, and operating procedures Review technical documents for accuracy, thoroughness and regulatory compliance Trains, coaches ...

  5. Associate Scientist (protein chemistry)

    Associate Scientist Morrisville NC 27560 6 month contract Pay rate: $21 - $24 per hour (based on experience) Specific Duties, Activities, and Responsibilities • Perform activities of moderate complexity involving others. Assist in the implementation of new technologies or approaches. • Occasional contact with customer technical personnel to effectively coordinate laboratory studies. • Writes summary reports with supervisory guidance. Can effectively coach or instruct technicians or lab ...

  6. 3919367 – QC Data Reviewer

    This position provides operational Phase Support organization of the QC Analytical, Biochemistry, and Raw Materials laboratory.  The successful candidate will plan and assist with required resources for day to day data review of raw data generated in the QC laboratories. You must have strong scientific and data review background as to provide technical knowledge and quality comments associated with raw data review and documentation.       RESPONSIBILITIES:   Perform timely data review with a ...

  7. Associate Scientist

      My name is Starr and I represent The Fountain Group.  We are a national staffing firm and are currently seeking an Associate Scientist for a prominent client of ours.  This position is located in Research Triangle Park, NC. Details for the positions are as follows:   Job Description:   Perform and document a variety of functions in support of the development of new technologies for cell culture manufacturing processes of human therapeutic biomolecules. Conduct laboratory cell culture ...

  8. Business Systems Analyst (7206)

    Qualifications: Bachelor's degree in Computer Science or related science or engineering field with 3-5 years experience Experience with software development lifecycle documentation and software testing in GxP environments. Experience supporting medical device testing services for GLP biocompatibility testing. Must be team oriented and have strong interpersonal skills and attention to details. Must have excellent written communication, organization and time management skills. Must be proficient with ...

  9. Director of Research & Development

    NW Recruiters is seeking a Director of Research & Development. This role will be responsible for driving step-change improvements in our client’s core technology, an all-natural, paper-based stick infused with pure fragrance, the best new passive diffusion product in the home fragrance industry. Collaborating with Marketing and Operations, the Director will also lead the development, refinement and execution of our client’s breakthrough technology development initiatives.​   Position Detail · We ...

  10. Clinical Document Specialist

      ~~SUMMARY: • The CDS will support the Company’s regulatory function and study team in the document management of clinical research trials from the project development stage through to project completion.  Mainly, the CDS will perform a variety of research, database, and administrative duties of a routine and technical nature in support of clinical trials to assist investigators in organizing, gathering, and compiling clinical research data. DUTIES AND RESPONSIBILITIES: • Assist with collecting, ...

  11. Regulatory Affairs Specialist

    ~~SUMMARY: • The Regulatory Affairs Specialist supports the Company’s regulatory function and project teams through the provision of a variety of administrative and technical tasks involving the management of clinical research trials documentation. In addition, the Regulatory Affairs Specialist performs a variety of research, database, and administrative duties of a routine and technical nature in support of corporate initiatives and clinical trials to assist MedSource and/or clients in organizing, ...

  12. Brand Leader---OTC based in Greensboro, NC

      Reporting directly to the Head of Commercial Operations, the Brand Manager will be responsible for all aspects of the development and execution of strategic and operational brand marketing plans for products in the consumer and physician markets including Blue Lizard Sunscreen.  The candidate will manage and be accountable for the overall performance of their brands including demand management and product Profit and Loss.   Knowledge, Skills and Experience required: BS/BA degree in business ...

  13. Brand Leader- Prescription Dermatology based in Greensboro, NC

      Reporting directly to the Head of Commercial Operations, the Rx Brand Leader will be responsible for all aspects of the development and execution of strategic and operational brand marketing plans for products in our branded dermatologic prescription division.  The successful candidate will manage and be accountable for the overall performance of their brands including demand management and product Profit and Loss. Knowledge Skills and Experience Required: BS/BA degree in business/marketing; ...

  14. Head Of Analytics based in Greensboro, NC

      Crown Laboratories,  Inc. is seeking a qualified business analyst who possesses high business acumen, understands pharmaceutical sales & marketing business processes and commercial data and has the ability to adapt to rapid growth and prosper in an entrepreneurial environment. Reporting directly to the Head of Commercial Operations, the Head of Analytics will be responsible for the development, preparation, quality assurance, distribution and maintenance of standard ad-hoc reports, including but ...

  15. 3910335 - GMP/GLP Analyst

      Job Purpose: Provide assistance to support the current effort of establishing a GMP testing laboratory within Analytical Development, which includes the initial setup, GMP certification and operational readiness.       Responsibilities:   Provides general administrative assistance to support change control records opened for the GMP lab Organize and maintain a list of current quality procedures for analytical laboratory operation, testing, method development, qualification and validation, ...

  16. Quality Control Associate

      My name is Starr and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Quality Control Associate for a prominent client of ours.  This position is located in RTP, NC. Details for the positions are as follows:   Job Description:   The primary responsibility for a Quality Control Associate I is the execution of QC environmental monitoring, routine testing and all activities associated with executing this testing in a cGMP manner. Additional ...

  17. Quality Assurance Manager GCP/GMP Operations

    Brio Resource Group is seeking a Quality Assurance Manager GCP/GMP Operations for an emerging pharmaceutical company located in the Raleigh/Durham, NC area. The QA Manager will be responsible for Clinical Trial Development projects and additional Quality Assurance Manufacturing activities.  Job Requirements: -Responsible for Clinical Supplies batch record review providing final release for use in clinical trials -Quality Assurance contact for deviations and failures -Clinical vendor selection ...

  18. Investigations Specialist

    Description PSC Biotech Corporation is a global, employee owned, life sciences consultancy that performs projects and staff augmentation in the following disciplines: Engineering, Information Technology, Technical Services, Validation, Compliance, Regulatory Submissions, Clinical, Project Management and Quality Assurance. PSC Biotech, incorporated in 1996, has been performing projects globally for over 15 years. PSC Biotech is currently looking for an Investigations Specialist for our client in ...

  19. 3888627 – QC Data Reviewer

    This position provides operational Phase Support organization of the QC Analytical, Biochemistry, and Raw Materials laboratory.  The successful candidate will plan and assist with required resources for day to day data review of raw data generated in the QC laboratories. You must have strong scientific and data review background as to provide technical knowledge and quality comments associated with raw data review and documentation.       RESPONSIBILITIES:   Perform timely data review with a ...

  20. 3881470 – QA Specialist

    Responsibilities:   Supports the development and maintenance of quality procedures, and systems related to Primary Manufacturing Quality Assurance oversight. Provides technical support for the US FCC site in all cGMP compliance related matters, including assurance that all aspects comply with cGMPs, legal, regulatory requirements, and the company Quality Manual requirements. Ensures that all aspects of USFCC operations comply with the requirements of the Quality manual and meets all relevant ...

  21. 3881470 – QA Specialist

    Responsibilities: • Supports the development and maintenance of quality procedures, and systems related to Primary Manufacturing Quality Assurance oversight. • Provides technical support for the US FCC site in all cGMP compliance related matters, including assurance that all aspects comply with cGMPs, legal, regulatory requirements, and the company Quality Manual requirements. • Ensures that all aspects of USFCC operations comply with the requirements of the Quality manual and meets all relevant ...

  22. Senior Field Service Technician

    Position Details: Job Title: Senior Field Service Technician Location: South Boston, VA 24592 Duration: 6-12+ months (Strong possibility for extension) Job Description / Requirement:  Prefer local people that would be willing to locate to South Boston or could make the drive when needed. (Surrounding NC and VA areas) Job Function: Installation and Commissioning Employment Contract Type: Regular/Permanent Basic Function:  Plan and execute, with minimal professional guidance, complex semi ...