- Aequor (Thousand Oaks, CA)
- …include evaluation of compliance issues, providing recommendations, and assuring progress of quality records to completion. The Sr. Associate will also represent ... perform GMP operations including following detailed SOPS, maintaining training, and good documentation practices. Also, ability to make Quality based decisions… 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
- 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
- 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
- Spectraforce Technologies Inc (Thousand Oaks, CA)
- Job Title: Senior Associate Quality Assurance Location: Thousand Oaks, CA Duration: 12 months Min PR starts from $33/hr Description: Onsite at the thousand oaks ... They will be working on the manufacturing floor. Detail Oriented, Team player and Quality Experience. The Sr. Associate Quality Assurance position supports… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Associate Clinical Research Associate - Northeast Region (Remote) With support of Senior Clinical Research Associate ... in a timely manner.Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out.Communicates with… more
- HITT Contracting (Falls Church, VA)
- …belong at HITT. Quality Control AssociateJob Description: The purpose of Quality Control Associate is to update and coordinate the planning, implementation, ... and supervision of the HITT quality control plan. This includes working with employees as...effective and timely corrective actions.Document and track all QC documentation including all required third party inspections and test… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Directive, and International Conference on Harmonization (ICH) guidelines. The Associate Director is accountable for operational planning and execution at ... planning start-up, conduct, reporting and close out) including timeline, quality and budget. A key focus will be the... of data is suitable for regulatory submission. The Associate Director will have routine interaction with key internal… more
- JobsRUs (Westbrook, ME)
- JobsRUs.comis seeking to hire a Quality Associate for our client in Westbrook, ME! Benefits Available!Weekly Pay! $19.00/HourShift: M-F 7- 3:30pm Description:In ... ANSI/ASQ Z1.4 preferredYou meet the physical requirements that go with working as a Quality Associate - Regularly required to stand and sit for extended periods;… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionWith support of Sr CRA (Clinical Research Associate ) and/or CRA Manager, acts as primary site contact and site manager-throughout all phases of a ... in a timely manner.-Collects, reviews, and monitors required regulatory documentation for study start-up, study-maintenance and study close-out.Communicates with… more
- Spectraforce Technologies Inc (Bothell, WA)
- …with regulatory and industry expectations. Assist the QA department in maintaining the Quality focused culture at Jump by ensuring documentation is complete, ... Title: Quality Assurance Specialist (Pharma ONLY - NON IT...Self Inspection auditing, QA reporting, and approval of GMP documentation . * Strong computer skills with Word and Excel… 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
- Southwest Research Institute (San Antonio, TX)
- …results for SWRI Divisions.The calibration of SWRI M&TE provides traceability and proper documentation for the various SWRI quality programs to be accredited to ... Are: The Institute Calibration Laboratory is a section of the Institute Quality Systems department. We are supporting Institute R&D divisions, service departments,… 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
- Merck & Co. (Durham, NC)
- Job Description Associate Technician - - Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a "Safety ... First, Quality Always" mindset striving for continuous improvement. We work...necessary for production . - Provides and/or authors all documentation and clerical functions necessary to allow proper accountability… more
- Merck & Co. (Rahway, NJ)
- …reliance on automation within Biologics Process Research & Development (BPR&D).The Associate Director role-will provide process automation leadership within the BDC ... -Execute and develop appropriate system validation, change control, and testing documentation in partnership with project CQV and IT teams.Establish GxP systems… 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)
- …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
- 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
- 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
