- Legend Biotech USA, Inc. (Raritan, NJ)
- …promise of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Document Control Specialist as part of the Quality team based in ... EU GDP/GMP, Part 11/Annex 11, PIC/S, MHRA).Operational experience with electronic quality systems.Experience with Document Management Systems (TruVault/Veeva) is… more
- Cipla (Hauppauge, NY)
- …products and packaging materials are stored within required conditions to maintain quality . Document and track any discrepancies found during inspections, ... 8:30am - 5:00pm Job Overview: The QA Inspector (Warehouse) ensures the quality and compliance of printed packaging materials and warehouse operations. This includes… more
- Insmed Incorporated (NJ)
- …and regulatory archives.Partner with cross-functional teams (Regulatory Affairs, CMC, Clinical, Quality ) to facilitate document authoring, review, approval, and ... requirements. The role has a strong focus on eCTD publishing and document management within Veeva Submissions Vault, ensuring accuracy, compliance, and timely… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …fieldSolid understanding of regulatory requirements, policies and guidelinesExperience with Quality Control document reviews and regulatory inspection ... QC Specialist, Lab Services, II/III as part of the Quality team based in Raritan, NJ. Role OverviewThe QC...on routine tasks and have conceptual understanding of all Quality Control functions and business areas. May need supervision/support… more
- 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 PM ... Salary Range : $64,272 - $77,662 PURPOSE The QA Document Control Associate in a pharmaceutical environment is responsible...Part 11, ICH, and ISO. This role supports the Quality Management System (QMS) by maintaining accurate, secure, and… more
- Twist BioScience (South San Francisco, CA)
- …Technical Writer - Temporary is responsible for directly participating in a Quality Systems Integration Program, with primary responsibility being the creating of ... high- quality content. The Technical Writer will interact with individuals at multiple levels within all functional departments, including Quality Assurance,… more
- Cipla (Central Islip, NY)
- … quality standards and regulatory requirements. Understanding of regulatory compliance, quality management systems and document control processes, and the ... of analytical techniques (HPLC, GC, UV-Vis etc.) and familiarity with quality control procedures. Responsible for performing routine analytical testing of raw… more
- Cipla (Hauppauge, NY)
- …and Logbook. Determine when to stop a line related to safety or quality . Operate automatic packaging equipment. Document packaging activities. Feed filling ... clearly, both written and verbally in English. Comply with safety and quality regulatory standards when packaging products.Ensure products are packaged in accordance… more
- Cipla (Fall River, MA)
- …requirements (eg, FDA, ). Maintain and ensure the proper documentation of all quality systems and records. Oversee document control processes, ensuring that SOPs ... an individual contributor role and a member of the InvaGen Pharmaceuticals Plant Quality Team. This role ensures compliance with both internal and external … 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 to Veeva.You ... the future of science, we're in. Are you?About the Role:We're looking for a Quality Management System (QMS) Specialist on the Analytical Development team to help us… more
