- Teva Pharmaceuticals (West Chester, PA)
- IT Business Process Analyst III Date: Jul 9, 2025 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals Job Id: 62740 **Who we ... a difference with. **The opportunity** We are currently recruiting an IT Business Process Analyst to support the local R&D laboratory computerised systems in West… more
- Novo Nordisk (Bloomington, IN)
- … Engineering Schedule: regular business hours You will work closely with process engineering, operations, manufacturing science & technology, validation , and IT ... is a state-of-the-art facility where we have an integrated model from process and formulation to clinical and commercial biomanufacturing and drug product… more
- Novo Nordisk (Bloomington, IN)
- …systems + Collaborate significantly with cross functional groups including Validation , Quality Control, Manufacturing, Process Development, and Facilities ... is a state-of-the-art facility where we have an integrated model from process and formulation to clinical and commercial biomanufacturing and drug product… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …to pilot plant and commercial-scale production, ensuring smooth technology transfer and process validation . + Has full accountability for all engineering aspects ... processes. + Responsible for authoring relevant sections of regulatory documents, validation plans, development reports, process flow diagrams (PFDs), piping… more
- Bristol Myers Squibb (Summit, NJ)
- …qualification and support requests. + Provides technical support and guidance on Validation , Quality Process , and equipment qualification issues. Interfaces with ... here at BMS with our Cell Therapy team. The Computer Systems Validation (CSV) Manager supports the successful implementation of manufacturing and laboratory… more
- VTI Life Sciences (Los Angeles, CA)
- …and critical process parameters. o Generate and review batch records and documentation. Process Validation o Conduct process validation studies to ... the LA site Responsibilities include but are not limited to the following: Provide validation support (IQ, OQ, PQ) for process vessels, buffer vessels, filter… more
- Charles River Laboratories (Memphis, TN)
- …related field. * Experience: 1-3 years of experience in computer system validation within a regulated industry ( pharmaceutical , medical device, biotechnology). * ... about. **Job Summary** BASIC SUMMARY: Responsible for computerized system validation activities within CRL Manufacturing Operations, including, but not limited… more
- Curia (Albuquerque, NM)
- …Minimum of five (5) years of progressively increasing responsibility in the pharmaceutical or biologics industry, with experience in validation activities, ... review and approval for qualification, validation , re-qualification, and re- validation documents for equipment and manufacturing process protocols,… more
- Fujifilm (College Station, TX)
- …**Qualifications:** + Master's Degree with 2+ years of direct experience in Validation in a pharmaceutical , biotechnology, or related industry, preferably in ... Bachelor's Degree with 4+ years of direct experience in Validation in a pharmaceutical , biotechnology, or related...who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any… more
- West Pharmaceutical Services (Williamsport, PA)
- …manufacturing. This role requires deep technical expertise in injection molding and process validation within a regulated, high-precision environment. The ideal ... molding techniques to ensure high-quality, repeatable manufacturing outcomes. + Oversee process validation activities (IQ/OQ/PQ) in compliance with ISO 13485… more
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