- Merck & Co. (Durham, NC)
- Job DescriptionWe are seeking a Growth and Improvement minded Quality Control Laboratory Associate Specialist that can help drive our Strategic Operating ... bulk active ingredient, finished product and support laboratory testing for vaccines.The Quality Control Laboratory Associate Specialist participates on a team… more
- Catalent (San Diego, CA)
- Quality Assurance Associate II - Manufacturing Catalent Pharma Solutions in San Diego is currently hiring a Manufacturing Quality Assurance (MQA) ... of activities pertaining to supporting, maintaining, and assuring compliance with quality systems requirements and applicable regulatory requirements; to advance the… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking Quality Systems Lead role as part of the Quality Operations team based ... in Raritan, New Jersey. Role Overview The Quality Systems Lead role is an exempt level position...approval of standard operating procedures and any other required documentation . Collaborate with functional departments to resolve issues. Perform… more
- Merck & Co. (Durham, NC)
- …in equipment validation, process validation, and GMP laboratory readiness.- The Quality Operations Laboratory Associate Specialist performs laboratory testing on ... laboratory investigations as needed and follows site procedures in the documentation of Quality Notifications and Corrective/Preventative ActionsExecute test… more
- Merck & Co. (Durham, NC)
- …6:30 AM ) rotation (2-2-3). - The VMF (Vaccine Manufacturing Facility) Associate Production Technician is an excellent entry-level opportunity for recent university ... through hands on processing activities. Key responsibilities for the Associate Production Technician include the execution of aseptic processing requirements,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …evolve, so does our challenge to find better and more innovative ways to improve their quality of life. We're changing lives for a living. Are you ready to make a ... Responsible for leading review and approval of training related materials, documentation and delivery of training for Patient Safety (PS) employees' onboarding… more
- Insmed Incorporated (Bridgewater, NJ)
- …Biopharma™, Best Workplaces in New York™, and Best Workplaces for Millennials™ lists.OverviewThe Quality Control Associate will serve as a strategic and tactical ... composing investigations as it pertains to testing and resultsAssists with documentation formatting. Formatting may include creating templates, fonts and style,… more
- Aequor (Thousand Oaks, CA)
- …in protein biochemistry and cell biology for the position of Process Development Associate , to join our Critical Reagent Group. The Critical Reagent Group serves our ... required for characterization, in-process and release testing of biological products. The PD Associate will work with a team of talented scientists to mainly lead… more
- Merck & Co. (Rahway, NJ)
- …of our Research & Development Division is seeking applicants for an Associate Principal Scientist position available at its Kenilworth, New Jersey research ... facility.- The Associate Principal Scientist is a laboratory-based scientific role tasked...in Analytical Methodologies and sound scientific understanding of Critical Quality Attributes/QbD/DOE principles as well as data analysis and… more
- Aequor (Newbury Park, CA)
- …in what we do. Detail oriented, to be able to monitor data quality . Comfortable learning new systems/processes. Someone who is able to follow instructions/guides, ... understands the importance of details, since we work so much with monitoring Data Quality and someone who is able to communicate clearly with internal and external… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …protocol amendments, site staff and location changes and IRB/REB/regulatory approvals to assure quality of the documentation files and compliance with NN SOPs, ... find better and more innovative ways to improve their quality of life. We're changing lives for a living....difference? The Position Drives the understanding & delivery of quality clinical research (patient safety, rights & wellbeing; data… more
- Merck & Co. (Millsboro, DE)
- …required.PurposeThe Associate Director/Attending Veterinarian will report to the Site Quality Head/Director of Quality . The Attending Veterinarian will be ... Delaware seeks to add an Attending Veterinarian in the role of Associate Director.This position will have overall responsibility for oversight and administration of… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …opportunity employer including veterans and people with disabilities. Summary The Associate Director, External Data Management, is accountable for the end-to-end ... on behalf of Daiichi Sankyo. This position also ensures quality delivery of all 3rd party data from diverse...programs. Is accountable for inspection readiness of external data documentation filed/archived in Trial Master File (TMF) according to… more
- Eisai, Inc (Nutley, NJ)
- …to hear from you.JOB SUMMARY:As a member of the Data Analytics group, the Associate Director, Commercial Analytics is part of a high performing team that provides ... for the department, and monitors compliance with these standards.Oversee data quality management process for assigned brand/s with external and internal data… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …The Position This position has primary responsibility to support operations for Quality Control at our biologics manufacturing facility. Assists in coordination and ... process and equipment improvement programs, creates technical reports, reviews completed quality records, generates quality comment and deviation responses and… more
- Insmed Incorporated (Bridgewater, NJ)
- …modalities.Assure bioanalytical tasks are executed to high scientific standards, with quality , and within agreed timelines. This entails overseeing work by internal ... to clinical development programs.Participate in clinical study design and documentation (lab manual, protocol, report, SAP)Participate in preclinical study design… more
- Aequor (South San Francisco, CA)
- …of organoid or other complex in-vitro model (CIVM) systems - Maintaining documentation related to protocol execution and results. - Writing protocols and ... as appropriate. - Adhering to departmental SOPs to ensure study integrity and quality . - Conducting experiments with a high level of independence and initiative. -… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking an Operations Associate (2nd Shift) as part of the Technical Operations team based in Raritan, ... within a CGMP environment. This position is responsible for quality and maintaining the highest standards in compliance within...information in a clear, concise, format according to Good Documentation Practices (GDP). Perform tasks on time in a… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …centered around rare diseases and immune disorders. Summary The CRA Oversight Associate Director plays an integral role in the strategic development, oversight, and ... a fast paced and results-oriented environment. This role will embody principles of Quality by Design (QbD) as it directly relates to risk-based monitoring (RBM) and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders.Summary The Associate Director, RACMC Portfolio Products, will be responsible for regulatory CMC ... applicable regulations. This includes preparation, review, and approval of CMC documentation for BLA Supplements (PAS, CBE-0, CBE-30), Annual reports, Lot… more
