- Actalent (Sanford, NC)
- Job Title: Manufacturing Quality Specialist Job Description We are seeking a Quality Assurance Associate to support a major pharmaceutical client. ... quality experience. Additional Skills & Qualifications + Experience with quality assurance in the pharmaceutical industry. + Knowledge of vaccine… more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- Analytical Quality Assurance Specialist Department: Analytical QA Location: Monroe, NC START YOUR APPLICATION ... emerge as a leading integrated research-based pharmaceutical company. POSITION SUMMARY: The Analytical Quality Assurance (AQA) Specialist will work with the … more
- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- Quality Assurance Specialist , Document Control Department: QA Manufacturing Location: Monroe, NC START YOUR APPLICATION ... : Under the direction of the QA Document Control Supervisor, the QA Specialist - Document Control, will control the movement, filing, archiving, and securing of… more
- Pfizer (Sanford, NC)
- **ROLE SUMMARY** This position provides Quality Assurance oversight for Quality Control (QC) Department. Provide QA ( Quality Assurance ) review and ... administered systems + Sound knowledge of current Good Manufacturing Practices (part of GxP) + Ability to work...process and/or interviewing. Requests for any other reason will not be returned. Quality Assurance and Control… more
- Actalent (Sanford, NC)
- …internal procedures. Required Skills: + Batch record review + GMP compliance + Quality assurance in pharmaceutical manufacturing Preferred Tools & Systems: ... Job Title: Quality Assurance Associate Location: Sanford, NC...clients. This role is critical to ensuring compliance and quality in biologics and vaccine manufacturing . The… more
- Biomat USA, Inc. (Research Triangle Park, NC)
- …Supports and assesses activities that ensure organizational adherence to corporate quality and compliance processes, including quality management systems ... with regulatory requirements, Standard Operating Procedures (SOP), current Good Manufacturing Practices (cGMP), and customer requirements. **Primary Responsibilities:** +… more
- Actalent (Sanford, NC)
- Description Actalent is seeking a Quality Assurance Associate to support one of our largest pharmaceutical clients. The QA Associate will be responsible for real ... time batch record review on the manufacturing shop floor as well as the other responsibilities...21CFR211 and internal procedures Skills batch record review, GMP, Quality , batch record, quality assurance … more
- Mentor Technical Group (NC)
- …Rico, Dominican Republic, Mexico, Germany, Canada, and South America. Responsibilities: + Quality Professional with Manufacturing Process Audit and Batch Record ... Review experience. + Available for non-standard shifts which include nights and weekends. + Basic knowledge of the process, PASx/MES application, MAXIMO, SAP, and LIMS. Education & Qualifications + Bachelor's degree and 5 years of directly related experience… more
- Catalent Pharma Solutions (Greenville, NC)
- **Pharmaceutical Manufacturing Specialist ** **Position Summary** Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical ... handling capabilities, ideal for orphan or targeted drug development. The Pharmaceutical Manufacturing Specialist has a primary focus on new technology and… more
- Actalent (Durham, NC)
- …Quality Specialist - Validation ensures adherence to current Good Manufacturing Practices (cGMP) and FDA Quality Systems throughout the evaluation, ... Quality Specialist - Validation Job Description...review, and approval of validation and quality assurance /control documentation. This role is essential… more