- Takeda Pharmaceuticals (Boston, MA)
- …is true to the best of my knowledge. **Job Description** **Job Title** : Associate Director , Clinical Quality Compliance **Location** : Cambridge, MA **About ... the role:** As the Associate Director , Clinical Quality Compliance,...guidance to other other non-GCP specific inspections (eg, GVP, GMP ). + Lead complex quality investigations improving… more
- Catalent Pharma Solutions (Chelsea, MA)
- ** Associate Director , Facilities** **Position Summary:** Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical industry ... in North America. Catalent Pharma Solutions is hiring an Associate Director , Facilities who leads the team...committed to a Patient First culture through excellence in quality and compliance, and to the safety of every… more
- Takeda Pharmaceuticals (Boston, MA)
- …management including CMC development strategy, regulatory submission strategy, quality /analytical control strategy, and specification justification strategy ( ... experience required + Analytical method development experience required + GMP and compliance experience required + Regulatory submission experience required… more
- ARCO (Framingham, MA)
- …and driving success at all levels of the business. We are looking for a Director of Food & Beverage Manufacturing to join our team of experts. Because ARCO is ... innovative solutions to enhance production, focusing on improvements in safety, quality , and efficiency for process/manufacturing end users + Establish profitable… more
- Nestle (Sudbury, MA)
- …for patients and consumers. **Position Summary:** Review all paperwork issued by Quality Associate before release for Production Department. Oversee the ... products manufactured and sold. Assist Product QA Supervisor & Quality Director in development of quality...programs. **Primary Responsibilities:** + Review of Receiving Paperwork and GMP documents. + Creation and review of all Bulk… more
- Nestle (Waltham, MA)
- …Summary:** Reporting to the Director , QA Donor Operations, the Principal Associate , Donor Operations Quality Assurance will work closely with our operational ... donor derived products. You will be involved in the quality support of collection facility personnel as well as...active, and creative problem solving. While this is a GMP environment, it is not your typical experience, our… more
- Astellas Pharma (Westborough, MA)
- …Manufacturing Specialist typically reports to a Manager, Sr Manager, or Associate Director of Manufacturing. **Essential Job Responsibilities:** + Responsible ... The Sr. Specialist, Manufacturing, will typically report a Manager, Sr. Manager, OR Associate Director of Manufacturing. This role is expected to Model our… more
- Astellas Pharma (Westborough, MA)
- …Manufacturing Specialist typically reports to the Manager, Sr Manager, or Associate Director of Manufacturing. **Essential Job Responsibilities:** + Responsible ... The incumbent will work with cross functional teams including Quality Assurance, Process Engineering, Supply Chain, and Manufacturing. The...will typically report to a Manager, Sr Manager, OR Associate Director of Manufacturing. This role is… more
- Takeda Pharmaceuticals (Boston, MA)
- …**Location** : Cambridge, MA **About the role:** You will report to the Associate Director Cell Therapy Microbiology QC. The Analyst, Cell Therapies QC ... of clinical-stage cell therapy drug products at an internal GMP facility. + Ensure that monitoring and testing are...At Takeda, our patients rely on us to deliver quality products. As a result, we must follow strict… more
- Astellas Pharma (Westborough, MA)
- …**Organizational Context:** The Senior Specialist, EHS will typically report to the Associate Director , Facilities and Engineering. This role is expected to ... permitting, and reporting, and updating hazardous materials inventory. + Knowledge of GMP cleanroom environments, Federal and State OSHA & EPA regulations, NFPA, and… more