, and change control. Proficiency in authoring and reviewing GMP documentation. Familiarity with environmental monitoring... of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud...
Lugar:
Dedham, MA | 26/07/2026 01:07:54 AM | Salario: S/. $42 - 52 per hour | Empresa:
Actalent to medical device or GMP-related industries, with understanding of regulated quality systems. Knowledge of process validation... & Qualifications Knowledge of GMP-related industries is preferred. Experience with quality system standards, including ISO 9001...
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Milwaukee, WI | 26/07/2026 01:07:52 AM | Salario: S/. $90000 - 100000 per year | Empresa:
Actalent and coordinate subcontractor and supplier participation. Develop and coordinate GMP budgets and bid packages. Maintain... and maintain strong relationships with owners, engineering consultants, subcontractors, and material suppliers. Propose and foster...
regulated cleanroom and GMP manufacturing environment. The role will primarily include putting raw materials into the machines... to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent...
QA Analyst (2nd Shift) Job Description The QA Analyst (2nd Shift) ensures product and process quality within a GMP... in Chemistry, Biology, or a related scientific field. 1–2 years of experience in a GMP manufacturing environment...
chromatography data, manages analytical documentation in compliance with GMP requirements, and contributes to method and analytical... document all GMP activities accurately and legibly, maintaining complete and compliant laboratory records. Perform routine...
Manufacturing Practice (GMP) guidelines, including 21 CFR Parts 210 and 211 and applicable ISO standards. Responsibilities Obtain... with quality control principles in a laboratory environment. Ability to learn and apply GMP guidelines, including 21 CFR Parts 210...
Lugar:
Newark, DE | 26/07/2026 00:07:03 AM | Salario: S/. $18 - 19 per hour | Empresa:
Actalent for production. Partner closely with Quality and Operations teams to release equipment into production in compliance with FDA, GMP... knowledge of FDA, GMP, and ISO 13485 requirements as they apply to automated manufacturing equipment and processes. Experience...
Lugar:
Irvine, CA | 26/07/2026 00:07:05 AM | Salario: S/. $120000 - 150000 per year | Empresa:
Actalent and final product samples. Skills GMP, PCR, Sample testing, Quality control, microbiology, qPCR, cell culture, mammalian... cell culture, Qc, Biology, Cgmp Top Skills Details GMP,PCR,Sample testing,Quality control,microbiology,qPCR,cell...
installations, modifications, and process improvements in a GMP-regulated pharmaceutical manufacturing environment. This role..., GMP, and internal quality system requirements throughout the project lifecycle. Own change control activities, including...