- Eurofins (Cambridge, MA)
- …technical transfer of ELISA-based assays and other validated methods into GMP laboratories, including training , troubleshooting, and procedural implementation. + ... ELISA-based potency assays-in full compliance with Good Manufacturing Practice ( GMP ) standards. This role ensures that methods are scientifically sound,… more
- Fujifilm (Holly Springs, NC)
- **Position Overview** The Sr. Specialist 2, Global QC Raw Materials GMP Support is responsible for supporting, leading, and participating in activities within ... **Job Description** **What You'll Do** * Creates, maintains, and improves GMP documents and processes in collaboration with stakeholders and QA *… more
- UCLA Health (Los Angeles, CA)
- Description The Human Gene and Cell Therapy Facility (HGCTF) Support Specialist will be responsible for overseeing the day-to-day laboratory activities including the ... tanks, and Medical/hazardous waste delivery and disposal. The Support Specialist will oversee the biannual/annual laboratory equipment maintenance activities. They… more
- Boehringer Ingelheim (St. Joseph, MO)
- …reflect Boehringer Ingelheim's high regard for our employees. The Principal Specialist , Validation manages all phases of higher level, more complex validation ... requirements and are suitable for their intended purposes. The Principal Specialist , Validation will lead project management efforts for validation activities… more
- Integra LifeSciences (Boston, MA)
- …and competencies of employees in a medical device-regulated environment. The Senior Training Specialist will assess training needs, develop curriculum, ... performance and align with Integra's core values. The Senior Training Specialist will collaborate with various stakeholders...with subject matter experts, that adhere to GDP and GMP standards. + Identifying training needs by… more
- Merck (Rahway, NJ)
- …enabling gain of critical internal experience with scale-up of manufacturing GMP steps, demonstration of new manufacturing technology/processes, training ... utility systems and associated infrastructure. Responsibilities of the Senior Specialist -Process Supervisor include the following: The process supervisor role… more
- Catalent Pharma Solutions (Harmans, MD)
- ** Specialist II, MTO** **Summary:** _Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, ... products including AAV and other viral vector-based therapies and vaccines._ The ** Specialist II, MTO** will provide support to Manufacturing Associates to meet… more
- Catalent Pharma Solutions (Harmans, MD)
- **Senior Specialist , QA OTF - Day Shift** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose ... including AAV and other viral vector-based therapies and vaccines. The Sr. Specialist , QA-OTF is responsible for providing Quality Assurance support for GMP… more
- Actalent (Boston, MA)
- …Specialist (25/hrs. per week) We are seeking a highly skilled QMS Specialist with experience in a GMP -regulated environment, ideally within biotech, cell/gene ... and effectively. In-depth knowledge of FDA, EMA, and ICH regulations for GMP compliance is essential. Responsibilities + Assess current QMS processes, identify areas… more
- Merck (Rahway, NJ)
- …Research Laboratories Division is seeking applicants for a Metrology and Validation Specialist position available at the Rahway, New Jersey research facility. The ... Metrology and Validation Specialist will work as part of the integrated US...routine maintenance of analytical equipment and instrumentation within the GMP environment. **The key responsibilities of this role will… more