- Merck (Rahway, NJ)
- **Job Description** ** Associate Principal Scientist - Microbiologist** Join us and experience our culture first-hand one of strong ethics & integrity, ... developing and expanding your career. In your role as Associate Principal Scientist , you will be a...deliver on critical data in a good manufacturing practices ( GMP ) microbiology laboratory including finished products testing, utilities, and… more
- Astrix Technology (Concord Township, OH)
- ** Associate Scientist , Method Development** Laboratory Concord, OH, US Pay Rate Low: 70000 | Pay Rate High: 80000 + Added - 06/05/2025 Apply for Job Our client ... chemical-based industries, and they're looking for a **Method Development Associate Scientist ** to join their growing team!...with at least 2 years of experience in a GMP analytical laboratory environment. + The ideal candidate will… more
- ManpowerGroup (Green Oaks, IL)
- Our client, a leading organization in the healthcare and biotechnology industry, is seeking an Associate Scientist I to join their team. As an Associate ... which will align successfully in the organization. **Job Title:** Associate Scientist I **Location:** Abbott Park, IL...in process and test method validations while adhering to GMP , ISO, and FDA regulations **What's Needed?** + Bachelor's… more
- Actalent (Sanford, NC)
- Job Title: Sr. Associate Scientist - Plate BasedJob Description The Sr. Associate Scientist will support the Quality Control Method Transfer and ... when required. + Support the technical leads and Sr. Scientist with project activities to meet deadlines. Essential Skills...activities to meet deadlines. Essential Skills + Experience with GMP in a pharmaceutical lab environment. + Proficiency in… more
- AbbVie (South San Francisco, CA)
- …The Cell Line Development Group in South San Francisco, CA is seeking an Associate Scientist II to join a talented and collaborative team developing CHO ... cell lines for GMP applications. In this laboratory position the candidate will...adherence to good documentation practices. Qualifications Basic Qualifications: + Associate Scientist II: BS with a minimum… more
- Lilly (Lebanon, IN)
- …build the processes and systems to enable a successful startup into GMP manufacturing operations._ **Organization Overview:** The Manufacturing Scientist is part ... to ensure safe and reliable supply of medicines. The Manufacturing Scientist executes technical projects (experimental, modeling and/or production data analysis) to… more
- AbbVie (South San Francisco, CA)
- …The Cell Line Development Group in South San Francisco, CA is seeking an Associate Scientist II to join a talented and collaborative team developing CHO ... cell lines for GMP applications. In this laboratory position the candidate will...and adherence to good documentation practices. Qualifications Required: + Associate Scientist II: BS with a minimum… more
- Sokol Materials & Services (Skillman, NJ)
- Associate Scientist Job Location Seattle, WA Workspace On-site position (no remote or hybrid options) Target Hiring Date August 11, 2025 Work Authorization ... per hour FLSA Classification: FT/PT | Non-Exempt/Exempt The primary focus of this Associate Scientist will be to support downstream process development and… more
- Genentech (South San Francisco, CA)
- …**Your Opportunity** In Cell Banking, we are seeking a highly motivated cell culture Associate Scientist to support various aspects of R&D and cGMP cell bank ... the Cell Banking processes in both the R&D and GMP environments, and providing scientific and technical judgment as...management documents for Cell Banking, as needed. + Support GMP operations **Who you are** + A Bachelor's/Master's holder… more
- Actalent (Birmingham, AL)
- Job Description We are seeking a dedicated and skilled Associate Scientist with experience in microbiological testing and validation support. This role involves ... testing. + Document test results and conclusions in a GMP manner and ensure test forms are complete before...Experience with LIMS/MIMS for tracking and entering data. + GMP documentation experience. + Ability to execute validation protocols… more