- Caris Life Sciences (Phoenix, AZ)
- …+ A minimum of 2 years of experience working within FDA regulated (Medical Device, Pharmaceutical) highly preferred and/or regulated industries (Automotive, ... Aerospace) preferred. + Experience in change management, as well as ensuring assets are appropriately addressed to remain in a validated state. + A Green Belt Certification in Six Sigma or similar certification preferred. + Demonstrated organizational,… more
- Bristol Myers Squibb (Devens, MA)
- …preferably with 1+ year of manufacturing site experience. Experience in FDA /EMA regulations in biopharmaceuticals or cell therapy manufacturing is preferred. ... **BMSCART** **\#LI-ONSITE** **GPS_2025** If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.… more
- Bristol Myers Squibb (Bothell, WA)
- …area management and co-workers + Basic understanding of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing is preferred ... **Shift:** Days - Sun - Tue (alt. Wed) 0500 - 1730 Days - Thu - Sat (alt. Wed) 0500 - 1730, Swing - Sun - Wed (alt. Sat) 1100 - 1130 Swing - Wed - Fri (alt. Sat) 1100 - 1130 **Working Conditions:** + Must be able to stand/walk for extended periods of time +… more
- Charles River Laboratories (Bethesda, MD)
- …worked on 80% of the drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. We're committed to providing benefits that elevate your ... quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.… more
- Jabil (Monument, CO)
- …preferred. + Medical device manufacturing, medical industry, or related FDA -regulated industry experience required. + Experienced in product/process validations ... which includes planning and executing Engineering Studies, Process Characterization, IQ, OQ, and PQ. Familiarity with change request processes. + Proficiency in use of personal computers, Microsoft Office products, and e-mail skills required. Experience with… more
- Stony Brook University (Stony Brook, NY)
- …oversight for clinical testing (CLIA, College of American Pathologists, FDA , NYSDOH). **Application Instructions** All application materials must be submitted ... online. Please use the Apply Now button to begin your application. For technical support, please visit Interfolio's Support Site ( https://support.interfolio.com/ ) or reach out to their Scholar Service Team at ###@interfolio.com or ###. For questions… more
- Abbott (Liberty, SC)
- …requirements. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, operating procedures, processes, ... and task assignments. + Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors. **QUALIFICATIONS** **Ability to work 2nd Shift: 4 days a week, 10 hours a day on** **weekdays: Monday… more
- Astrix Technology (Los Angeles, CA)
- …+ Follow all safety, cGMP, and regulatory guidelines to ensure compliance with FDA and industry requirements. + Assist in inventory management by verifying raw ... material availability and reporting shortages. **Qualifications:** + High school diploma or equivalent required; technical or vocational training a plus. + 1-3 years of experience in compounding, cosmetics, skincare, pharmaceuticals, or related manufacturing… more
- Adecco US, Inc. (Marlborough, MA)
- …including Occupational Safety and Health Administration (OSHA), Quality System Regulations ( FDA ), ISO 13485, MDD, PAL, CMDCAS, KFDA, other country specific ... Regulations as applicable. **Requirements:** . 3 - 5 Years with BA 1 - 3 Years with MBA. . Prefer Five years experience with staffing/recruitment for direct labor and professional experience. . Exposure to manufacturing environments. . Strong written and… more
- Bristol Myers Squibb (Manati, PR)
- …Key Stakeholders. + Collaborates on an exception basis with government regulatory agency ( FDA , Customs) in the event of site inspections. + Works with Planner / ... Buyer to assure execution of materials requirement process to support agreed production plan. **Qualifications & Experience:** + BA/BS in Supply Chain, Business Administration, or Engineering. + Five or more years of work-related experience in manufacturing… more