- American Red Cross (Douglasville, GA)
- …and resolving errors, issues, and customer concerns. Drive continuous process improvement and manage suspect product/sample protocols. + **Technical Expertise** ... : Support validation of hardware, software, instrumentation, and procedures. Serve as...of supervisory orleadexperience. + **Preferred Background** : Experience in pharmaceutical manufacturing is a plus. + **Skills** : +… more
- Caris Life Sciences (Phoenix, AZ)
- …logic, and system narratives for BMS controlled assets. + Support validation , qualification, and commissioning of BMS components and controlled spaces, including ... automation engineering, or facilities engineering in a regulated life sciences, pharmaceutical , biotech, or clinical laboratory environment. + Bachelor's degree in… more
- Cambrex High Point (Charles City, IA)
- …regulatory compliance. Responsibilities + Serve as a subject matter expert for In- Process and Finished Goods Analytical Records (AR) and Batch Records (BR) review ... stakeholders, and regulatory inspections. + Review and approve Method Validation , Analytical Development, and Method Development reports, providing compliance and… more
- Sanofi Group (Framingham, MA)
- …Clean Steam, Clean-In-Place (CIP) systems, autoclaves, glassware washers, and related process support equipment. + Perform preventative and corrective maintenance on ... orders, PMs, and calibration/verification records. + Collaborate with Engineering, Validation , Metrology, and Quality Assurance to support investigations, projects,… more
- ThermoFisher Scientific (Detroit, MI)
- …testing activities. + Support manufacturing through batch record review, in- process quality monitoring, and collaboration with operations personnel. + Participate ... prior experience in a Quality Control Laboratory setting in the Pharmaceutical /Biotech/Life Science industry. + Experience performing routine testing and supporting… more
- Fujifilm (Warminster, PA)
- …+ Responsible for the performance of the Quality Management Systems (includingQA/ Validation /Doc control)of the organization. + Trend, Analyze Quality Indicators and ... + 10 or more years of direct Quality Systems experience in the pharmaceutical , medical device and/or Bio sciences industry + 5+ years of Management experience.… more
- Mentor Technical Group (Gurabo, PR)
- …and South America. Responsibilities: + Review and approve product MPs. + Approve process validation protocols and reports for manufacturing processes. + Request ... MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines. With offices… more
- Cardinal Health (East Hartford, CT)
- …of quality, analytical metrics and / or statistics, trending, quality planning, validation , CAPA and problem solving. + Works cross-functionally and has the ability ... material controls, laboratory controls, packaging and labeling, and production & process controls. + Establishes and reports metrics related products and processes… more
- Cardinal Health (Seattle, WA)
- …of quality, analytical metrics and / or statistics, trending, quality planning, validation , CAPA and problem solving. + Works cross-functionally and has the ability ... material controls, laboratory controls, packaging and labeling, and production & process controls. + Establish and report metrics related products and processes… more
- Keurig Dr Pepper (Columbus, OH)
- …This role serves as a senior technical resource, leading complex validation and verification activities, driving continuous improvement, and ensuring full alignment ... quality systems and drive sustainable improvements. **Certifications & Training** + Better Process Control School certification + Lean Six Sigma (Yellow, White, and… more
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