- Eurofins US Network (Rensselaer, NY)
- …monitoring** in cleanrooms and controlled areas to ensure compliance with cGMP standards. + Collect samples from **high-purity water systems** , clean ... **Minimum Requirements** + **Bachelor's degree** in Biology or related field OR ** Associate 's degree** in Life Sciences with relevant experience. + Ability to meet… more
- Unither Pharmaceuticals (Rochester, NY)
- …It has more than 280 employees. Your role Reporting to the Quality Director , JOB SUMMARY: This is a team-oriented position with the individual actively coordinating, ... with the approved report(s) within the appropriate project folder throughout the process of validating a system. Develop a standard operating procedure specific to… more
- Bristol Myers Squibb (Manati, PR)
- …needs. 17. Leadership Continuity Serves as the designated backup for the Associate Director of Drug Product Operations during absences, ensuring continuity ... Productivity & Continuous Improvement Champions productivity initiatives by identifying process efficiencies and allocating resources to support cross-functional improvement… more
- Merck (West Point, PA)
- …individual contributor, under the supervision of a Senior Specialist or Associate Director . **Additional Responsibilities** + Provide technical manufacturing ... areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation. We are… more
- Lilly (Indianapolis, IN)
- …instrumental in the success of the safety culture. Working cross functionally, the Associate Director Engineer excels at relationship building at all levels of ... supervises a small but growing team for all engineering, technical process improvements, warehouse maintenance, Health, Safety, and Environmental (HSE), and security… more
- Bristol Myers Squibb (Devens, MA)
- …Relationship** This role is stationed in Devens, MA and reports to the Associate Director of Quality Engineering for the Devens Cell Therapy Facility. ... qualification, and validation (CQV), computer systems validation (CSV) and process validation per established local and global standards. **Duties/Responsibilities**… more
- Merck (West Point, PA)
- …the West Point vaccine manufacturing site. The Specialist, with guidance from the Associate Director of Environmental Monitoring Site Support, ensures AVS are ... cGMP Compliance, Computer Information, Computer Technology, Continual Improvement Process , Data Analysis, Decision Making, Documentation Review, Documentations, Environmental… more
- ADM (Forsyth, MO)
- …during shift. + Works with necessary groups to resolve outstanding issues with process documents / logbooks, cGMP walk through inspection observations and ... of Quality Systems. The Quality Assurance Specialist, with guidance from the Director of Quality Assurance, performs duties required to maintain the Quality Systems,… more
- Sanofi Group (Waltham, MA)
- …to join the R&D Automation team in Waltham, MA. Reporting to the Automation Associate Director , this position is responsible for providing day to day and ... project-based automation support for both cGMP and non-GMP groups within the R&D organization located...+ Provide technical solutions to a wide range of process automation related design challenges. + Work collaboratively with… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …part of the Materials Science team in Franklin Lakes NJ, reporting to the Associate Director , Materials Science. Our R&D Engineers and Scientists are responsible ... microbiology labs. + Comprehensive knowledge of the medical device product development process under a quality management system in a regulated environment (ISO… more