- Merck & Co. (Rahway, NJ)
- …by a dedicated application designed to create a frictionless flow of data from source systems to regulatory documentation.- - - Under the guidance of dCMC ... Regulatory Authoring Leadership, the Senior Specialist , ...- Required Skills and Experience: Knowledge of manufacturing, testing, quality , and supply chain processes from late clinical development… more
- Insmed Incorporated (NJ)
- …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 ... and develop key metrics on documentation status and compliance using the Veeva Quality Management System to ensure alignment with regulatory and internal … more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …labels and documents prior to use on the manufacturing floor.Utilize multiple electronic quality systems , batch records and SAP.Work in a team based, ... multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist III as part of the Quality ...as needed.Consistently perform tasks in adherence with safety policies, quality systems , and cGMP requirements, as well… more
- Aequor (Golden Valley, MN)
- Job Title: Packaging Development Specialist Location: Golden Valley, MN 55427 (Hybrid) (temp-to-hire)Duration: 12 Months Shift: M-F Job Title: Packaging Development ... Specialist - Integrated Project Solutions About the Role: This...collaborate with cross-functional teams (Marketing, Suppliers, Food Safety & Quality , and R&D) to launch new products and packaging… more
- Cipla (Fall River, MA)
- …and completeness. Defends the validation programs and strategies to customers and regulatory auditors. Performs weekly quality reviews of Master Control database ... Job Title : Pkg. Documentation Specialist II FLSA Classification : Professional, Exempt Work...company's document and SOP's procedures while ensuring their accuracy, quality , and integrity. This position reports to the Department… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …actions.Perform tasks in a manner consistent with the safety policies, quality systems , and cGMP requirements.Drive continuous improvementOther duties may ... immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking a QA Validation Specialist III as part of the Quality team based in Raritan, NJ.Role… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …Biotech is seeking QC Specialist , Lab Services, II/III as part of the Quality team based in Raritan, NJ. Role OverviewThe QC Specialist , Lab Services is ... Biology, Biochemistry, Microbiology, Chemistry or related fieldSolid understanding of regulatory requirements, policies and guidelinesExperience with Quality … more
- Highmark Health (Pittsburgh, PA)
- …monitoring, compliance and/or regulatory processes 2 years experience with quality measurement systems 1 year experience evaluating, implementing or revising ... entity. Gathers information and prepares reports in response to inquiries from regulatory agencies and/or internal customers. Quality Reviews and provides input… more
- Merck (Salem, OR)
- …a dedicated application designed to create a frictionless flow of data from source systems to regulatory documentation. Under the guidance of dCMC Regulatory ... Specialist , Regulatory Authoring Business Analyst, will optimize regulatory authoring processes and enhance data management by mapping workflows, prioritizing… more
- Advancial (Dallas, TX)
- …the company's affirmative action plan, please complete this form. SUMMARY The Regulatory Reporting Financial Specialist is responsible for compiling, analyzing, ... mission is to create lasting value for our members through superior service, quality products, and innovative solutions. At Advancial, we always strive to provide… more
