- Actalent (St. Louis, MO)
- …electronic Quality and Training Management Systems. + At least 1 year of experience with batch record review and GMP documentation in a pharmaceutical GMP ... Job Title: Document Control Administrator III Job Description As a...efficiency within our operations. Responsibilities + Scan and archive batch records and other cGMP documents. + Organize, pack,… more
- Catalent Pharma Solutions (Manassas, VA)
- ** Document Control Specialist ** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission ... complex formulations to help create engaging new products consumers will love. The ** Document Control Specialist ** is responsible for creation and maintenance of… more
- Astrix Technology (Los Angeles, CA)
- …for extension The QA Document Control Specialist will manage document control activities to ensure compliance with GMP and regulatory requirements. ... **QA Document Control Specialist ** Clinical Pharmacology Los...Biology, or related field + 2+ years of QA document control experience in GMP biotech/pharma +… more
- Actalent (Boston, MA)
- Job Title: Technical Quality Assurance Senior Specialist Job Description The Technical Quality Assurance Senior Specialist will oversee and ensure the quality of ... including change control, supplier onboarding, analytical method transfer and validation, document readiness, and more. The position also requires collaboration with… more
- Astrix Technology (Dallas, TX)
- …in pharma or related industry, with 2+ in sterile manufacturing preferred + Strong GMP knowledge and experience reviewing batch records + Skilled in SOP writing ... **QA Specialist II** Quality Control Dallas, TX, US Pay... II** , you'll be the quality gatekeeper for GMP manufacturing-reviewing critical documentation, inspecting materials, and ensuring every… more
- dsm-firmenich (Kingstree, SC)
- **Senior Specialist , Quality Assurance** **Location: Kingstree, SC** **Onsite** As a **Senior Specialist ** within our Quality team, you will be responsible for ... providing administrative support to the Quality department through document creation and revision, audit support, and the entire document retention program. You… more
- ThermoFisher Scientific (Plainville, MA)
- …updates on outstanding commitments. * Ensures the quality of and supports all GMP manufacturing activities. * Review of completed batch records in accordance ... hr shift/days **Environmental Conditions** Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail… more
- Actalent (Boston, MA)
- …Quality Assurance Senior SpecialistJob Description The Technical Quality Assurance Senior Specialist will oversee various quality aspects related to tech transfer ... involves collaboration with Quality management to define and execute batch disposition strategies, ensuring comprehensive quality oversight throughout tech transfer… more
- The Estee Lauder Companies (Bristol, PA)
- **Description** Quality Operations Specialist is responsible for quality assurance activities related, but not limited to, incoming raw materials & components, ... leading deviation handling, root cause analysis and CAPA development, conducting document reviews to verify effectiveness of procedures and instructions, and… more
- Dairy Farmers of America (Richmond, IN)
- **Job Description** **GENERAL PURPOSE** Review specifications, procedures, protocols, and batch records for Good Manufacturing Procedures (GMPs) compliance to ... and state regulatory review findings . File and maintain batch production and control records . Inform management of...issues are found. Ensure that supervisors fully explain and document production deviations . Document and update… more