- Cytiva (Miami, FL)
- …manufacturing and design, ensuring compliance with regulatory standards and driving process improvements; leading root cause analysis and CAPA initiatives, ensuring ... nonconformances to maintain product quality and customer satisfaction; overseeing manufacturing validation (IQ, OQ, PQ) and design assurance activities to support… more
- Eurofins (Raleigh, NC)
- …areas of bio/ pharmaceutical manufacturing, including method development, microbiology, process validation and quality control. Position Summary Eurofins BPT ... Eurofins is the world leader in the bio/ pharmaceutical testing market. With over €6.5 billion in...Sales Manager to join our team, focusing on facility validation and environmental monitoring solutions for the biopharmaceutical and… more
- Eurofins (Lancaster, PA)
- …areas of bio/ pharmaceutical manufacturing, including method development, microbiology, process validation and quality control. Job Summary: Eurofins Small ... Eurofins is the world leader in the bio/ pharmaceutical testing market. With over €5.3 billion in...seeking candidates with expertise in method development and/or method validation . + Applies GMP in all areas of responsibility,… more
- Eurofins (Lancaster, PA)
- …areas of bio/ pharmaceutical manufacturing, including method development, microbiology, process validation and quality control. Job Summary: Are you ... Eurofins is the world leader in the bio/ pharmaceutical testing market. With over €5.3 billion in...develop your career? Eurofins Small Molecule Method Development and Validation team is seeking an entry level scientist to… more
- Bristol Myers Squibb (Summit, NJ)
- … pharmaceutical industry. + Minimum of 8 years' experience performing/supporting pharmaceutical computer systems validation on pharmaceutical equipment or ... with our Cell Therapy team. T he Associate Director, Computer Systems Validation (CSV), Equipment Commissioning & Qualification (ECQ) supports the activities and… more
- Danaher Corporation (Fargo, ND)
- …development and delivery of solutions that safeguard and improve human health. The Process Validation Engineer II is part of the Technical Operations Department ... discoveries worldwide. You will be a part of the Process Validation team and report to the...company + Knowledge of regulatory and cGMP regulations for pharmaceutical manufacturing operations and validation procedures and… more
- System One (Piscataway, NJ)
- …installations, and process changes by ensuring proper qualification and validation for pharmaceutical and biopharmaceutical production. + Author ... or related field). + Minimum 4+ years of experience in facilities validation , commissioning, and qualification (CQV) in the pharmaceutical or biopharmaceutical… more
- VTI Life Sciences (Raleigh, NC)
- …for 2 Cleaning Validation Engineers to work onsite at our client's pharmaceutical manufacturing facility in the Raleigh, NC area. One (1) Cleaning Validation ... Senior Cleaning Validation Engineer. Job Title: Cleaning Validation Engineer Industry: Pharmaceutical Manufacturing Level of...such as, but not limited to, operations, QA, QC, process support, supply chain, etc and gain alignments as… more
- Astellas Pharma (Westborough, MA)
- …for commissioning and qualification of facilities/utilities, equipment, automated systems, and process validation . + Author, execute, review, and approve ... validation documentation for facilities/utilities, equipment, automated systems, and process validation and assist with resolving technical issues, evaluating… more
- Fujifilm (College Station, TX)
- …final qualification requirements of TOP's for GMP facilities. + Single Use and Process Validation a plus. + Excellent written and oral communication skills. ... with qualification/computer validation experience. + Experience with qualification/ validation of process equipment, clean utilities, automation, sterile… more
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