Jobs: MasterControl

  • Document Control Specialist

    Found in: Lensa US P 2 C2 - 7 days ago


    Portage, United States System One Holdings, LLC Full time

    Title: Document Control Specialist Location: Portage, IN Schedule: Mon-Fri, 8am-5pm Type: Contract Start: ASAP Overview: The Document Control Specialist coordinates and maintains the company's Document Control and Training system. Strictly follows established company policies and procedures to ensure compliance with pharmaceutical industry regulations and...

  • Document Control Specialist

    Found in: Talent US C2 - 6 days ago


    Salt Lake City, United States Sotera Health Full time

    The Document Control Specialist administers the global document control process for multiple Nelson Labs locations; including the revision, approval, and archival of controlled documents. This position also supports the laboratory by processing customer testing instructions and works in a collaborative environment to effectively and efficiently meet the...


  • Houston, United States Quest Energy Group Full time

    Job DescriptionJob DescriptionQuest (www.questenergygroup.com) is a leader in Executive Search and Talent Acquisition in the Energy Industry.We are currently recruiting for a Document Control Specialist with oil and gas /maritime construction / construction related background. The Document Control Specialist will lead Document Control functions; storage and...

  • Document Control Specialist

    Found in: Lensa US P 2 C2 - 7 days ago


    Salt Lake City, United States Sotera Health Services, LLC Full time

    Job Description The Document Control Specialist administers the global document control process for multiple Nelson Labs locations; including the revision, approval, and archival of controlled documents. This position also supports the laboratory by processing customer testing instructions and works in a collaborative environment to effectively and...


  • Oceanside, United States CCS INC Full time

    Job DescriptionJob DescriptionQualificationsBachelors degree in Science or equivalent work experience.3-4 years working in a GXP or ISO regulated environment.1-2 years in a Quality Assurance related role.Working experience in internal or supplier audits and hosting external auditsExperience with EQMS or EDMS (MasterControl) preferredASQ certification such as...


  • Philadelphia, United States EPM Scientific Full time

    My client is a rapidly growing biotech organization in the Philadelphia Area and is looking to hire a QA, Document Control and Training - Specialist to manage the team's manufacturing documents.Key responsibilities:Managing Documents: Keep track of important documents in the Electronic Document Management Systems, making sure they're reviewed, approved, and...

  • Quality Assurance Specialist, Document Control and Training

    Found in: Appcast Linkedin GBL C2 - 4 days ago


    Philadelphia, United States EPM Scientific Full time

    My client is a rapidly growing biotech organization in the Philadelphia Area and is looking to hire a QA, Document Control and Training - Specialist to manage the team's manufacturing documents.Key responsibilities:Managing Documents: Keep track of important documents in the Electronic Document Management Systems, making sure they're reviewed, approved, and...

  • Quality Assurance Scientist

    Found in: Lensa US P 2 C2 - 7 days ago


    High Point, United States Cambrex Full time

    Overview: Position performs daily QA activities to support GMP Analytical projects, nonGMP/GMP Manufacturing Facility operations, and other duties as needed. Responsibilities: Perform approval process for analytical procedures. Perform approval process for analytical protocols/reports. Maintain controlled documents. Perform approval and release of regulated...

  • Quality Assurance Scientist

    Found in: Resume Library US A2 - 6 days ago


    High Point, North Carolina, United States Cambrex Full time

    Overview: Position performs daily QA activities to support GMP Analytical projects, nonGMP/GMP Manufacturing Facility operations, and other duties as needed. Responsibilities: Perform approval process for analytical procedures. Perform approval process for analytical protocols/reports. Maintain controlled documents. Perform approval and release of regulated...

  • Training Specialist

    6 days ago


    Paulsboro, United States Veranova L P Full time

    Job DescriptionJob DescriptionCompany DescriptionVeranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation.Job DescriptionThe Training...


  • Omaha, United States Cordova Full time

    Job DescriptionJob DescriptionTechnology's Future Depends On Innovators Director of IT We have a fantastic opportunity for a Director of IT who will be responsible for managing all of the manufacturing Information Technology Systems and department. The right candidate will interact with different levels of management and personnel within each department. The...


  • Bridgewater, United States Kelly Science, Engineering, Technology & Telecom Full time

    Kelly Technology is looking for a MES Configuration Analyst - Direct Hire - Hybrid in Bridgewater, NJ. This position is open with our client, one of the leading medical devices companies, operating globally.Title: MES Configuration Analyst - CamstarLocation: Bridgewater, NJClient Industry: Biomed / Medical DevicesDirect Hire 3 days/week on site...


  • Monroe, United States Glenmark Pharmaceuticals Inc. Full time

    Job DescriptionJob DescriptionUnder the direction of the QA Document Control Supervisor, the QA Specialist – Document Control, will control the movement, filing, archiving, and securing of all documents with the objective of ensuring compliance to company policies and procedures. In addition, the QA Specialist will review, issue, and reconcile controlled...

  • MES Camstar Configuration Analyst

    Found in: Appcast Linkedin GBL C2 - 6 days ago


    Bridgewater, United States Kelly Science, Engineering, Technology & Telecom Full time

    Kelly Technology is looking for a MES Configuration Analyst - Direct Hire - Hybrid in Bridgewater, NJ. This position is open with our client, one of the leading medical devices companies, operating globally.Title: MES Configuration Analyst - CamstarLocation: Bridgewater, NJClient Industry: Biomed / Medical DevicesDirect Hire 3 days/week on site...

  • Principal Quality Engineer

    Found in: Lensa US P 2 C2 - 7 days ago


    Needham Heights, United States CareerBuilder Full time

    Evolved By Nature team is seeking a Principal Quality Engineer, responsible for driving and supporting all aspects of the quality system, quality through new product introductions, and quality within manufacturing. This position reports into the Senior Director, Quality, and is based in Needham, MA. Responsibilities:Actively participate in the product...

  • Document Controller

    1 hour ago


    Boulder, United States CORDEN PHARMA BOULDER INC Full time

    Job DescriptionJob DescriptionEQUAL OPPORTUNITY EMPLOYERCorden Pharma provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation,...


  • Winchester, United States BioIVT Full time

    Job DescriptionJob DescriptionWe are a leading global provider of high-quality biological specimens and value-added services. By combining technical expertise, exceptional customer service, and unparalleled access to biological specimens. Our mission is to provide high quality biological tissues, fluids, cell products, and services to our customers to...

  • Data Entry Operator

    Found in: beBee jobs US - 3 hours ago


    Southaven, Mississippi, United States Labcorp Full time

    Job DescriptionLabCorp is looking for a Clinical Data Entry Operator to join our Southaven, MS lab. The Data Entry Clerk works in a fast-paced, production-type environment. Learn about the laboratory science industry as you enter data vital to the laboratory process.SHIFT:Tuesday-Saturday, 3 am – 11:30 a.m. PRINCIPAL FUNCTIONAL RESPONSIBILITIESThe...

  • QA Specialist

    55 minutes ago


    Orange County, United States BioPhase Solutions Full time

    Job DescriptionJob DescriptionBioPhase Solutions specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a QA Specialist to work for an Orange County area contract manufacturing company.Pay Rate: $25-35/hour depending on experience.Summary:Review GMP technical documentation to ensure...


  • Spring Lake, United States Northern Biomedical Research Inc Full time

    Job DescriptionJob DescriptionRole SummaryThe Necropsy Coordinator will engage in the improvement and advancement of Necropsy Operations through identification, planning and implementation of projects and improvement activities. The Necropsy Coordinator is responsible for communicating expectations, business needs and opportunities for improvement to...