- Aldevron (Miami, FL)
- …a part of the Operational Quality Assurance team and report to the Sr . Manager, Operational QA, responsible for Developing and implementing labeling processes and ... and external vendors to ensure timely and accurate labeling production , including translations, barcodes, and serialization.Ensure that labeling content, format,… more
- Houston Methodist (Houston, TX)
- At Houston Methodist, the Sr . Current Good Manufacturing Practices ( cGMP ) Specialist is responsible for adherence to Standard Operating Procedures (SOPs) and ... cGMP regulations pertaining to the manufacture of therapeutics and...proper guidance of junior level team members. As a senior member of the department, this position will actively… more
- University of Southern California (Los Angeles, CA)
- …cell and gene therapy products, identifies equipment and components necessary for cGMP production , implements necessary changes to the process and reagents ... cGMP Process Development (PD) SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP -Process-Development--PD-- Specialist \_REQ20159663/apply) Keck School of Medicine Los… more
- Regeneron Pharmaceuticals (Rensselaer, NY)
- Regeneron is currently looking for a Drug Production , Senior Manufacturing Specialist in the Global Manufacturing department. In this role, you will focus on ... world while working in a clean room environment. A typical day for a Drug Production , Senior Manufacturing Specialist might include: + Performing all aspects… more
- Merck (Elkhorn, NE)
- **Job Description** Join our IPT Teams (Central Services, Warehouse and Packaging) as the Sr . Specialist of Operations in Elkhorn, NE! The Sr . Specialist ... to effectively communicate problems, causes and suggested corrective actions. The Specialist will review and audits manufacturing records for errors and ensure… more
- Boehringer Ingelheim (St. Joseph, MO)
- …using office application software (MS-Word, MS-Excel, MS-Outlook, PowerPoint). **Requirements for a Sr . Specialist Validation** + A BS degree from an accredited ... reflect Boehringer Ingelheim's high regard for our employees. The Principal Specialist , Validation manages all phases of higher level, more complex validation… more
- Boehringer Ingelheim (Barceloneta, PR)
- …of manufacturing and/or packaging situations while maintaining compliance with cGMP 's, safety and environmental regulations, and company standards and policies. ... 2 Board process. + Acts as key user for Production Execution for the ERP, as assigned. **Requirements** +...+ Six (6) or more years of experience in production , technical or maintenance areas. + Knowledge and practical… more
- Boehringer Ingelheim (Barceloneta, PR)
- …to cost control, cost reduction, inventory control, and effectiveness of production systems. Identifies strengths and weak points, defines and recommends improvement ... using Lean Six Sigma & continuous improvement methodologies in regulated manufacturing environment ( cGMP ). + Lean Six Sigma Green or Black Belt certification. + PMP… more
- Colgate-Palmolive (Topeka, KS)
- …plant level, working collaboratively with cross-functional teams to ensure production meets stringent microbiological standards and operating procedures. The ... mitigation strategies to reduce microbiological risks, including cleaning, sanitization, cGMP , and preventive controls. - Support FSMA initiatives and regulatory… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …more than 110 countries and regions. **Shift** : 1st - M-F 8:00am - 4:30pm ** Sr . Quality Associate I/II - Summary:** The Sr . Quality Associate I/II will ... primarily serve as a Quality Systems technical specialist as part of the QA Fractionation business unit....medium complexity and developing solutions for defined problems. The Sr . Quality Associate I/II will also perform manufacturing record… more
