- Merck & Co. (Rahway, NJ)
- …review and approval of documentation to support Good Manufacturing Practice ( GMP ) clinical supply API manufacture, testing, release, and maintenance in support ... to API manufacturing in a complex, clinical supply development.- Review and/or approve GMP documents. Ensure all API are manufactured in compliance with cGMP and… more
- Aequor (East Syracuse, NY)
- …preferred. Working knowledge and experience in the biopharmaceutical development process, GMP , PAT, CMC and regulatory guidance, ICH guidelines, and compendial ... and coordinating timely transfer of test methods with and to Quality Control laboratories is desired. Specific Knowledge, Skills, Abilities, etc. Strong written,… more
- Eisai, Inc (Exton, PA)
- …into the production suites.The Associate Director writes, reviews, and/or approves GMP documents, including validation protocols and reports, and SOPs, along with ... Development groups as well as with Facilities, Quality Assurance, Quality Control , Regulatory, and CMC Program Management departments.The Associate Director of… more
- ManpowerGroup (Rockville, MD)
- Our client, a leader in the pharmaceutical industry, is seeking a Pharma Document Control Associate to join their team. The ideal candidate will have strong ... will align successfully in the organization. **Job Title:** Pharma Document Control Associate **Location:** Rockville, MD **Pay...per respective SOP. + Archive and maintain GLP and GMP documents with an accurate inventory, both on and… more
- Lilly (Lebanon, IN)
- …within a GMP -regulated environment. **Additional Preferences:** + Strong knowledge of GMP regulations and document control processes. + Experience with ... ( GMP ) library, document inventory, ensuring true copy accuracy, and overseeing document control within our electronic document system. This role also… more
- Catalent Pharma Solutions (Harmans, MD)
- …are met and leading continuous improvement initiatives. The Document Control function supports both the GMP and development operations. Catalent, ... support Phase I/II/III/commercial operations. + Manages document control processes and systems for GMP activities...document control processes and systems for GMP activities in compliance with internal procedures and policies,… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- Quality Assurance Specialist, Document Control Department: QA Manufacturing Location: Monroe, NC START YOUR APPLICATION ... POSITION SUMMARY : Under the direction of the QA Document Control Supervisor, the QA Specialist -...study Experience : + 0-2 years of Pharmaceutical and FDA/ GMP industry experience is preferred. + Previous Quality experience… more
- Herbalife (Lake Forest, CA)
- QA Document Control Coordinator (1st Shift) Category: Quality Position Type: Regular Full-Time External ID: 17057 Location: Lake Forest, CA, United States Date ... LinkedIn share to linkedin Apply Now **Overview** **THE ROLE:** The First Shift Quality Document Control Coordinator will work onsite at our state of art… more
- Integra LifeSciences (Princeton, NJ)
- …to advance patient outcomes and set new standards of care. The Sr. Manager, Document Control and Training is responsible for leading the Corporate Document ... position is also responsible for assessing, developing and maintaining the Corporate Document Control and Training Administration Programs in compliance with US… more
- Actalent (Random Lake, WI)
- Job Title: Document Control Specialist Job Description We are seeking a dedicated Document Control Specialist to manage and create Pallet Tag IDs for all ... NetSuite. Essential Skills + Experience in quality assurance and quality control . + Familiarity with GMP , FDA, and USDA regulations. + Knowledge of food safety… more
- AECOM (Abilene, TX)
- …but are not limited to GMP buyout review process, cost related document control , invoice process, change order process, contingency usage, limitations, and ... provided in UNIFORMAT II and CSI format. + Undertake GMP finalization exercise following the completion of GC bid...to the actual work carried out identifying any final GMP savings. + Work with GC and construction management… more
- Promotion In Motion (Somerset, NJ)
- …+ Conduct GMP inspections to ensure compliance. + Monitor, verify and document Critical Control Points (CCP) for Food Safety. + Recommend improvements to ... Quality Control Technician Job Details Job Location Somerset -...to Plant management and SQFP + Follow PIM Brands GMP rules + Monitor fellow employees for adherence to… more
- Regeneron Pharmaceuticals (Rensselaer, NY)
- We are hiring a Lead Document Coordinator to assist our Document Control team! As a Lead Document Coordinator, you will provide support to the process of ... controlling and maintaining documentation to ensure effective and efficient application of GMP . Documentation within this process includes, but is not limited to,… more
- FreshRealm (Lancaster, TX)
- …to support the production/warehouse team and the entire facility up to and including GMP enforcement, allergen control , food defense and line checks. + Work with ... in Lancaster, TX. FreshRealm is looking for a Quality Control Associate that will perform quality checks and tasks...QC associates on standard operating procedures (food safety, GMP , allergens, CCPs, food defense, PPE / hygiene policies)… more
- Stanford University (Stanford, CA)
- … performance of analytical methods in order to be consistent with current GMP and documentation practices. + Support document revision/creation in collaboration ... Quality Control Associate I **School of Medicine, Stanford, California,...Adhere to requirements of the method and good documentation practices. Document and maintain environmental monitoring data and generate monitoring… more
- Cambridge Isotope Laboratories, Inc. (Andover, MA)
- Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Senior Quality Control Analyst I based onsite in our Andover, MA facility. CIL is the global leading ... Group and has had consistent growth for over 40 years. The Senior Quality Control Analyst I is responsible for providing direction, guidance and training to QC… more
- Cambridge Isotope Laboratories, Inc. (Andover, MA)
- Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Control Analyst II, based onsite in our Andover, MA facility. CIL is the global leading company ... had consistent growth for over 40 years. The Quality Control (QC) Analyst II is responsible for conducting routine...is responsible for conducting routine and non-routine analysis of GMP and ISO materials under general supervision and in… more
- Aerotek (Vernon Hills, IL)
- …Perform quality control checks on food products. + Ensure compliance with GMP and quality assurance standards. + Document quality assurance processes and ... 2 years of food quality experience + Knowledge of GMP standards + Proficiency in quality control ...of GMP standards + Proficiency in quality control and assurance **Additional Skills & Qualifications** + Spanish… more
- Kelly Services (Lodi, CA)
- …process efficiency initiatives, and pursue long-term growth within the quality control department. **Key Responsibilities:** + Perform and document laboratory ... **Kelly(R) Science & Clinical is seeking a Quality Control Analyst I for a premier client in...responsible for finished product testing activities in accordance with GMP standards and FDA/ISO regulations. This role offers the… more
- Actalent (Berkeley, MO)
- …regular audits and inspections, ensuring all activities meet EHS requirements. Conduct GMP testing in an analytical laboratory environment using HPLC and UPLC test ... + Author and/or review SOPs, test methods, forms, etc., in the document management system eDMS. + Ensure compliance with Standard Operating Procedures, Good… more
