- 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
- Kelly Services (Rockville, MD)
- …a GMP -regulated, fast-paced environment. **Key Responsibilities** + Execute and document manufacturing batch records, SOPs, and work instructions + Operate ... **Associate Specialist - Cell Therapy Manufacturing** **Pay Rate:** $25.00...- Cell Therapy Manufacturing)** to support the start-up and GMP operations of a state-of-the-art **cell therapy manufacturing facility**… more
- Merck (Elkhorn, NE)
- …Technical Support, Planning, and Maintenance to ensure alignment of goals. + Update batch records and procedures as per GMP requirements. + Provide support ... a highly motivated individual to fill the position of Associate Specialist Downstream Improvement and Support, within our Manufacturing Division. This position… more
- Bristol Myers Squibb (Devens, MA)
- …MES, SAP, ValG, DeltaV, Maximo, Infinity, etc.). + Should be familiar with GMP -related systems including Quality Risk Management, Document and Data Governance, ... to Manufacturing, Quality Control laboratories, and Warehouse Operations. The **Senior Specialist , Quality Assurance Shop Floor, Cell Therapy** position will oversee… more
- Kelly Services (Greendale, IN)
- **Job Title:** Quality System Specialist **Location** : Greendale IN- 100% Onsite **Duration:** Temp to perm **Pay Rate:** $30-$35/hr. **Shift:** MON-FRI 8 HOURS A ... **Position Overview:** + Our client is seeking a temporary Quality Management Systems Specialist to join our dynamic Quality Assurance team at our Greendale, Indiana… more
- Adecco US, Inc. (Greendale, IN)
- **Light Industrial Position** + **Job Title:** Quality System Specialist (Temp-to-Hire) + **Requirements:** Steel toe shoes + **Pay:** $30-$35/hour + **Schedule:** ... 7:00, 8:00, or 9:00 AM) **I. Position Summary** A **temp-to-hire Quality System Specialist ** is needed to join the Quality Assurance team at the Greendale, Indiana… more
- Kemin Industries (Lenexa, KS)
- …Hennessy Research Associates - a Kemin Company is hiring a Quality Assurance Specialist . As a Quality Assurance Specialist with Hennessy Research Associates, you ... the disposition of finished products, raw materials and packaging. + Review batch records and laboratory analysis results for accuracy and completeness. +… more
- Kelly Services (St. Louis, MO)
- **Technical Documentation Specialist - Manufacturing (Contract)** **Join a Leader in Infection Prevention and Make Your Mark on Quality!** Are you a skilled ... for clarity and compliance? We're seeking a meticulous and experienced Technical Documentation Specialist to join our team in St. Louis! This 3+ month contract role… more
- Kelly Services (South San Francisco, CA)
- …EMA, ICH, GMP ) and quality management principles. + Experience with Document Control, Complaint and Supplier Management Systems. + Must have startup experience. ... **Senior Quality Systems Specialist ** Kelly(R) Science & Clinical is seeking a...implementation and oversight of key quality systems, such as Document Control, Supplier Management, Deviations and Complaints. + Collaborate… more
- Amgen (Thousand Oaks, CA)
- …Join us and transform the lives of patients while transforming your career. ** Specialist Manufacturing** **What you will do** Let's do this. Let's change the world. ... **Responsibilities:** + Initiate, revise, and approve manufacturing-controlled documents in the document management system. Serve as document author, owner,… more
- Catalent Pharma Solutions (Manassas, VA)
- **Quality Assurance Specialist I** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission ... soft chews for nutritional supplements and nutraceuticals, as well as small batch lozenges. With extensive development and manufacturing expertise and a wide range… more