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  1. Automotive Technician / Mechanical Associate at CarMax

    Auto Tech must re a d, inter p ret and tra n scribe data in order to mainta i n accurate r e cords. Re q uir e s wa l k ing o r sta n d i ng for an ext e nded p...

  2. Manager/Sr. Manager, Financial Planning & Business Operations at Infinity Pharmaceuticals

    Infinity is an innovative biopharmaceutical company dedicated to discovering, developing and delivering best-in-class medicines to people with difficult-to

  3. Corporate Communications Specialist at Infinity Pharmaceuticals

    Experience working in biotech or pharmaceuticals is required. Prepare reporter briefing documents for executive spokespeople and assist with speaker coaching...

  4. Firmware Engineer at Optikos Corporation

    Motion controllers, LCD displays, DACs, A/Ds, I/O controls, PWM controls, PID loops. Bachelor or higher degree in computer science or a relevant engineering or...

  5. Database Administrator SQL DBA at Lahey Clinic

    Qualifications Bachelor's degree in Computer Science. Assists with the formulation, documentation and publication of organizational standards governing database...

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    1. Clinical Regulatory Publishing Mgr III eCTD Regulatory Affairs 98402-1

      Job Description:A Clinical Project Publishing Manager III is needed for a contract position at major pharma company in Northeast.About Client:My client is a global company within the pharmaceutical industry operating in 10 states within the U.S. and a leader in the pharmaceutical industry. They are a progressive and growing company with a diversified line of products. My client has a dynamic ...

    1. Global Therapeutic Head MS Regulatory Affairs Genzyme at Genzyme

      Global Therapeutic Head, MS Regulatory Affairs, Genzyme-00470272-56561 Description Genzyme has pioneered the development and delivery of transformative

    1. Quality Control Analyst III

      My name is Jennifer Carroll and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Quality Control Analyst III for a prominent client of ours.  This position is located in Framingham, MA. Details for the position are as follows: Job Description: This position is responsible  for performing some routine  and complex techniques associated with  daily QC ...

    1. Clinical Compliance Manager at Ocular Therapeutix, Inc.

      Performing quality control review on clinical trial documents to ensure accuracy, consistency, and completeness where possible....

    1. QA Compliance Specialist II

      Job Title:  QA Compliance Specialist IIReports To (Title):Manager, Associate Director, Director Function:Quality Compliance Department: Oncology & Biologics QualityOBJECTIVES:  Assists in coordination of activities to ensure Quality Compliance; works cross-functionally with other departments, Alliance Partners and company Affiliates to ensure compliance with corporate and regulatory ...

    1. QA Manager (Biotech) at Solid Biosciences

      QA Manager (biotech) Solid GT, LLC (Solid GT) is looking for an experienced QA Manager in the biotechnology industry with an entrepreneurial spirit, drive

    1. Product Labeling Consultant

      A leading pharmaceutical company in Cambridge, MA is seeking a Product Labeling Consultant. This position within the Global Supply Chain is responsible for managing pharmaceutical labeling projects supporting international and domestic clinical trials. The individual is responsible for activities to develop, create, and implement clinical trial product labeling in over 50 countries. Other ...

    1. Protein Biochemist at Biotech Industry Organization

      We are a private biotechnology company based in the Boston area. As we begin to launch commercial operations, we are accelerating hiring at our Woburn R&D

    1. Labeling Consultant

      Hello, My name is Chrys and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Labeling Consultant  for a prominent client of ours.  This position is located in  Cambridge, MA  Details for the position are as follows: Job Description:This position within the Global Supply Chain is responsible for managing pharmaceutical labeling projects supporting ...

    1. HR Manager at PixarBio Corporation

      Organizes, leads and documents post-interview feedback with interview teams. Recruiting, benefits administrations, payroll, labor relations experience in a...

    1. Manager – Clinical Labeling Project

      Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis. Title: Manager – Clinical Labeling ProjectJob ID: 7097Industry: Biotech/PharmaceuticalUnit: Global Supply ChainLocation: Cambridge, MADuration: 3 Month ContractPay Rate Range: ...

    1. Senior Mechanical Engineer at Seahorse Bioscience

      Motion control and automation. Provide documentation and design control for mechanical systems. Automation and motion control systems (pneumatic actuators,...

    1. Assembly Worker

       Candidate Pay rate is $15/hr. Qualifications:High school diploma or equivalent, six months related experience preferred. Experience with manufacturing. Experience with medical device manufacturing a plus, but not required. Responsibilities: 1. Builds: ú Build devices per written protocol and approved deviation. ú Ability to follow work instructions and operate semi-complex equipment as ...

    1. Acquisitions Editor for JoVE Engineering at JoVE

      Our approach to scientific publishing has been adopted at leading universities and biotech companies in the USA, Europe and Asia....

    1. Quality Control Technician

      Description: The Quality Assurance Professional will work in the Internal QA team of Human Genetic Therapies Quality Assurance Department. Responsibilities include QA issuance of GMP documentation including manufacturing batch record and logbooks. Maintain all logs and files associated with documentation issuance process. Some limited review of executed manufacturing batch records may also be ...

    1. Software Engineer - GUI at NeuroLogica

      R & D – Software Engineering. BS in Computer Science or equivalent and 3+ years of experience preferred. Responsible for the development and maintenance of...

    1. Sr. Manager (Associate Director) Quality, GLP

       The Sr. Quality Manager of GLP is responsible for assisting with the strategic alignment of projects and activities and refining those projects and/or activities proactively. This role is also responsible for technical development of personnel and ensuring the quality of deliverables within their purview.Key Responsibilities:• Accountable for regulatory compliance and ensuring procedures are ...

    1. Vice President, Accounting at Infinity Pharmaceuticals

      A minimum of 10 to 12 years of progressively responsible financial leadership experience in the pharmaceutical or biotech industry....

    1. Senior Process Engineer

      Senior Process Engineer - Lexington, MA DescriptionPrimary Duties: The individual will be expected to monitor and provide support for upstream manufacturing operations. Responsibilities will include design, implementation and daily review of production operations and data trends, process event response and troubleshooting, deviation/investigation support, ownership of quality system ...

    1. Senior Project Engineer at Cold Chain Technologies, Inc.

      Experience servicing the pharmaceutical and biotech markets. Cold Chain Technologies (CCT) is a leading developer and manufacturer of controlled-temperature...

    1. Technical Writing Compliance Administrator

      Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis. Title: Technical Writing Compliance AdministratorJob ID: 2424Industry: Biotech/PharmaceuticalLocation: Frederick, MDDuration: 12 monthHours per Week: 40 Responsibilities: Follows ...

    2. Medical Information Director - Oncology Compendia Specialist

      Lead team that oversees compendia submissions and responds to unsolicited requests from patients, healthcare providers and payers for information on Oncology Therapeutics while ensuring that information is accurate, complete and fair balanced evidence based. *** Coordinate the dissemination of product information both external customers (healthcare professionals, consumers, payers, etc.) ...

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      No Telecommute

    3. Quality Control Manager - (98349)

      1-Position summary a) Work with contract testing sites, perform methods transfers and support methods troubleshooting b) Support method validation activities internally and externally c) Author, review and revise documents and respond to methods related regulatory agency questions 2-Specific Duties & responsibilities - Perform methods transfers and troubleshooting particularly IXAZOMIB to ...

    4. Automation Engineer

      This is a contract position that will provide support for a growing automation group. The person in this role will be supporting processes, utilities, and building automation systems used in commercial production. This position requires experience in working within a cGMP operation, especially regarding change control and other quality systems. The candidate must be technically proficient in ...

    5. Quality Assurance - Lot Release Specialist

      Mid-senior level lot release specialist with 5+ years of experience in the biopharma industry. Specific experience in the Quality organization with focus on lot disposition activities such as batch record review, quality systems review (change controls, CAPAs, deviations etc.), lot tree analysis etc. is required. Experience with other quality functions including document control, ...

    6. QA Documentation Specialist

      Quality Assurance Documentation Specialist Lexington, MA (USA) Kelly Scientific Resources (KSR) is currently seeking a highly motivated QA Documentation Specialist for a key support role with one of our top clients in Lexington, MA.As a Quality Assurance Documentation Specialist placed with Kelly Scientific Resources, you will report to the Corporate Quality Compliance Director and be ...

    7. Production Technician

      The Suspension Preparation Cleaner is a direct labor position reporting to the Suspension Prep PET Process Facilitator, which supports Suspension and Filling operations in the disinfection of classified areas. The position entails performing cleaning and disinfection activities in a controlled area, stocking of necessary gowning for use in the controlled area, supporting Suspension ...

    8. Firmware Engineer

      Principal Embedded SW lead engineerReports To:Manager, Software Engineering Department:  General Position Summary: This position is responsible for designing, implementing, and validating the software for Client Ventricular Assistance Device systems (VAD)Essential Functions/Major Responsibilities:• Designs, codes, and debugs implantable or external embedded software and/or corresponding ...

    9. Firmware Engineer

      Principal Embedded SW lead engineerReports To:Manager, Software Engineering Department:  General Position Summary: This position is responsible for designing, implementing, and validating the software for Client Ventricular Assistance Device systems (VAD)Essential Functions/Major Responsibilities:• Designs, codes, and debugs implantable or external embedded software and/or corresponding ...

    10. Systems Engineer

      PRINCIPAL SYSTEMS ENGINEER:Our large Medical Device client, based in Middlesex County, Massachusetts, is seeking a Principal Systems Engineer. This is a full time, permanent role at a very competitive salary. General Position Summary:This position is responsible for designing, implementing, and validating the Client Ventricular Assistance Device system.Essential Functions/Major ...

    11. Medical Writer- Medical Imaging

      We are looking for a Medical Writer with experience in Medical Imaging. A qualified candidate would have 3-5 years of writing experience with a Medical Imaging background (preferred) or Pharmaceutical background. The writer will be working with the medical team to write charters, the agreement between the sponsor and Medical Imaging department. •           Write documents associated with ...

    12. Analytic Coordinator

      Reports to:    Director of Epidemiology and Outcomes Research (DEOR)Summary of Position: The Analytic Coordinator will be involved with research projects that include patients with musculoskeletal, rheumatic and other inflammatory diseases and conditions as well as dermatologic patients. Responsibilities include working closely with subscriber investigators to carry out queries and research ...

    13. Automation Engineer

      This is a contract position that will provide support for a growing automation group. The person in this role will be supporting processes, utilities, and building automation systems used in commercial production. This position requires experience in working within a cGMP operation, especially regarding change control and other quality systems. The candidate must be technically proficient in ...

    14. Sr. Manager (Associate Director) Quality, GLP

       The Sr. Quality Manager of GLP is responsible for assisting with the strategic alignment of projects and activities and refining those projects and/or activities proactively. This role is also responsible for technical development of personnel and ensuring the quality of deliverables within their purview.Key Responsibilities:• Accountable for regulatory compliance and ensuring procedures are ...

      1. Regulatory Affairs Specialist at NeuroLogica

        Bachelor’s in Engineering, Biological Sciences, or Related field preferred. Provide regulatory input and guidance on standards, design controls, and Quality...

      2. Administrative Coordinator at ADINA R & D

        If you are interested in working with us at ADINA R & D, please contact Dr. ADINA R & D believes strongly in maintaining an excellent work environment with a...

      3. Regulatory Affairs Technical Writer at Genpact Pharmalink

        Specific focus is on Chemistry, Manufacturing, and Controls (CMC). Bachelor’s Degree or higher in life sciences field4+ yrs biologics CMC Reg Affairs experience...

      4. Technical Writer - Control Systems & Embedded Systems at The MathWorks

        Proven ability to explain complex engineering or science concepts clearly. An experienced technical writer with a strong engineering or computer science...

      5. Epic Ambulatory Applications Manager at Lahey Clinic

        Analyze time spent in relation to work assigned / expectations and promptly address discrepancies or issues as required.3.Facilitate Electronic Health Record (E...