- Abeona (Cleveland, OH)
- QUALITY CONTROL RAW MATERIALS - ANALYST II Department: Quality and Compliance Reports to: Supervisor or Manager, Quality Control Description: The Quality ... activities in support of Good Manufacturing Practices (GMP) testing for Quality Control (QC). Performs raw material release testing. Supports the authorship and… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …Some off-shift based on business need - 8 hours Shift_ **IGIV-C Material Control Tech/Tech II** **Summary** **:** The IGIV-C Material Control Operator ... uninterrupted production of IGIV-C. **Primary responsibilities for IGIV-C Material Control Operator/Tech** **:** + Departmental SAP subject matter expert responsible… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- Quality Control Analyst Department: Chemistry Location: Monroe, NC START YOUR APPLICATION ... is for a highly motivated member of the Quality Control (QC) Lab at the Monroe manufacturing facility, reporting...Biochemistry Experience: - 1-3 years in the field of Pharmaceutical (manufacturing facility). - Background in the functional areas… more
- Actalent (Frederick, MD)
- Job Title: Quality Control ChemistJob Description We are seeking a dedicated Quality Control Chemist who will play a crucial role in ensuring the quality and ... with 2+ years of experience in biotechnology or related field and Quality Control experience, or High School Degree with 3+ years of experience in biotechnology… more
- Abeona (Cleveland, OH)
- Job Title Quality CONTROL Analyst II Department Quality and Compliance Reports to Supervisor or Manager, Quality Control DESCRIPTION Position Overview The ... activities in support of Good Manufacturing Practices (GMP) testing for Quality Control (QC). Performs in-process and release testing for drug substance and drug… more
- Teva Pharmaceuticals (West Chester, PA)
- Microbiology Senior Quality Control Associate Date: May 20, 2025 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals Job Id: ... apply scientific/technical standards, principles, theories, concepts and techniques of bio- pharmaceutical drug development and GxP requirements. * Display sound… more
- Endo International (Rochester, MI)
- …current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. May train less senior staff. **Job Description** Scope of ... manner conforming to regulatory, company and compendiaI requirements within pharmaceutical manufacturing setting + Document accurately data generated in… more
- Astrix Technology (Indianapolis, IN)
- **Document Control Specialist** Science & Research Indianapolis, IN, US Pay Rate Low: 28.85 | Pay Rate High: 31 + Added - 21/03/2025 Apply for Job **Documentation ... Control Specialist** Monday-Friday 8a-5p/9a-6p/10a-630p Must be flexible with schedule...docs from eQMS (batch record, training forms, etc.) - Pharmaceutical experience strongly preferred This job description is a… more
- Actalent (Parsippany Troy Hills, NJ)
- Job Title: Document Control Specialist Job Description Join our team as a Document Control Specialist where you will play a crucial role in managing and ... overseeing the document control processes within our organization. Your primary tasks will...knowledge, preferably with GxP Documents. + Clinical, research, or pharmaceutical experience is advantageous. + Technical writing experience within… more
- Lilly (Indianapolis, IN)
- …better for people around the world. **Organization Overview:** The Global Quality Control - Deviation Mentor plays a critical role within the Analytical Sciences ... and Quality Control (QC) organization. This individual is responsible for guiding...+ Minimum of 5 years of experience in the pharmaceutical or biotechnology industry. + Proven expertise in leading… more