- Cipla (Fall River, MA)
- Job Title : QA Document Control Associate FLSA Classification : Full-Time, Professional Work Location : Fall River, MA Work Hours: General Shift: 08:30 AM - 5:00 ... Salary Range : $64,272 - $77,662 PURPOSE The QA Document Control Associate in a pharmaceutical environment...controlled documents to ensure compliance with GMP, GDP, and regulatory standards such as FDA 21 CFR Part 11,… more
- Twist BioScience (South San Francisco, CA)
- …departments, including Quality Assurance, Regulatory Affairs, Supplier Quality , Supply Chain, Quality Control , Production, Process Development, ... in a GMP, Biotechnology, Pharmaceuticals or another Regulated Industry.Experience in Quality Assurance/ Regulatory requirements in medical devices, IVD, EU… more
- Cipla (Central Islip, NY)
- … standards and regulatory requirements. Understanding of regulatory compliance, quality management systems and document control processes, and the ... knowledge of analytical techniques (HPLC, GC, UV-Vis etc.) and familiarity with quality control procedures. Responsible for performing routine analytical testing… more
- Insmed Incorporated (NJ)
- … archives.Partner with cross-functional teams ( Regulatory Affairs, CMC, Clinical, Quality ) to facilitate document authoring, review, approval, and publishing ... content and metadata within Veeva Submissions Vault, ensuring compliance with document management standards, version control , and audit readiness.Coordinate the… more
- Merck & Co. (Rahway, NJ)
- …CMC regulatory content Understanding of CMC operations, technology transfer, control strategy development, and regulatory authoring requirements that inform ... Preferred Experience and Skills Experience implementing or supporting automated regulatory authoring (structured content, template-driven generation, or document … more
- Insmed Incorporated (NJ)
- …You Are:You have a Bachelor's degree along with 2+ years of experience ona document control team using a quality management system, with preference ... and develop key metrics on documentation status and compliance using the Veeva Quality Management System to ensure alignment with regulatory and internal … more
- Cipla (Fall River, MA)
- …programs and strategies to customers and regulatory auditors. Performs weekly quality reviews of Master Control database by assuring new documents have ... the company's document and SOP's procedures while ensuring their accuracy, quality , and integrity. This position reports to the Department Head - Manufacturing… more
- Merck & Co. (Rahway, NJ)
- …CMC regulatory content Understanding of CMC operations, technology transfer, control strategy development, and regulatory authoring requirements that inform ... Preferred Experience and Skills Experience implementing or supporting automated regulatory authoring (structured content, template-driven generation, or document … more
- Cipla (Fall River, MA)
- …programs and strategies to customers and regulatory auditors. Performs weekly quality reviews of Master Control database by assuring new documents have ... company's document and SOP's procedures while ensuring their accuracy, quality , and integrity. This position reports to the Manufacturing/Packaging and partners… more
- Cipla (Hauppauge, NY)
- …product integrity. Affixing approved labels on the approved materials, once release from quality control after testing. Review and verify artwork proofs for ... products and packaging materials are stored within required conditions to maintain quality . Document and track any discrepancies found during inspections,… more
