- 3D Systems, Inc. (Rock Hill, SC)
- …manufacturing operations, preferably in the medical device industry under FDA /ISO 13485 design controls. Candidates should be comfortable working in ... the methodical, structured, and well-documented manner expected in a highly-regulated industry. Solid understanding and background in core manufacturing engineering fundamentals, such as process development, light design work, data analysis, statistics,… more
- Bristol Myers Squibb (Princeton, NJ)
- …device, biologics) facilities and have worked for the US Food & Drug Administration ( FDA ), within the past 10 years (2015-2025) in a Consumer Safety Officer (CSO) or ... similar role; minimum of 5 years' experience as a CSO required. * Demonstrated negotiation, risk management, relationship management and conflict resolution skills. * Proven ability to understand complex processes/problems and propose alternate solutions. *… more
- Actalent (Richmond, VA)
- …and identify new opportunities. Essential Skills + Proficiency in GMP, and FDA compliance. + Experience in preventive maintenance and continuous improvement. + ... Skilled in PLC troubleshooting and programming. + Strong knowledge of electrical engineering and reliability engineering. + Familiarity with lean manufacturing principles. Additional Skills & Qualifications + Background in industrial manufacturing. +… more
- TE Connectivity (Medway, MA)
- …environment. * Prior management/supervisor experienced preferred * Working knowledge of FDA /ISO/MDD Quality systems for medical device companies. * Excellent written ... and oral communication skills essential **Competencies** Values: Integrity, Accountability, Inclusion, Innovation, Teamwork **ABOUT TE CONNECTIVITY** TE Connectivity is a global industrial technology leader creating a safer, sustainable, productive, and… more
- United Therapeutics (Research Triangle Park, NC)
- …their daughter's pulmonary arterial hypertension (PAH). Today, we have six FDA -approved therapies that treat PAH, pulmonary hypertension associated with interstitial ... lung disease (PH-ILD) and neuroblastoma, a rare pediatric cancer. Our near-term pipeline seeks to develop additional therapies for PAH and pulmonary fibrosis (PF). The cure for end-stage life-threatening diseases like PAH, PH-ILD, PF, and many others is an… more
- Danaher Corporation (Chaska, MN)
- …test method, equipment, process, and/or design testing methodologies. + Knowledge of FDA regulations, ISO standards, and GxP guidelines. + Experience with Computer ... System Validation (CSV) and process validation It would be a plus if you also possess previous experience in: + Experience in IVD Medical device or Pharmaceutical Manufacturing + ASQ Certification Beckman Coulter Diagnostics, a Danaher operating company,… more
- Lilly (Indianapolis, IN)
- …of pharmaceutical industry regulations and compliance requirements (eg, PhRMA, FDA ). + Familiarity with medical affairs activities, including KOL engagement, ... medical education, and publication planning. + Excellent written and verbal communication skills, with the ability to convey complex scientific information clearly and concisely to diverse audiences + Strong analytical and critical thinking skills. +… more
- Aerotek (Hazelwood, MO)
- …in technical matters. + Working knowledge of OSHA, GFSI, QF, USDA, and FDA regulations. **Why Work Here?** Join a startup company that offers tremendous growth ... opportunities. Be a part of a dynamic team within a cutting-edge facility. **Work Environment** The position is based in a food manufacturing plant, offering a flexible shift schedule and requiring adherence to safety and quality standards. **Job Type &… more
- Grifols Shared Services North America, Inc (San Marcos, TX)
- …+ Plan and conduct scheduled internal audits to assess compliance with FDA , ISO, MDR, and internal requirements. To include audit scheduling, investigation, and ... evaluation of audit observation and findings, reporting, follow-up, and confirmation of follow-up actions. + Pro-actively investigate, identify, and implement best in class Quality Systems practices and implement/manage improvement projects within the… more
- Actalent (Madison, WI)
- …and Analyst software. + Knowledge of ICH or 28BMV regulatory guidance protocols and FDA internal standards. Job Type & Location This is a Permanent position based ... out of Madison, WI. Pay and Benefits The pay range for this position is $85000.00 - $110000.00/yr. Medical Plan* No Charge Laboratory Testing Benefit and physical therapy Dental Plan Vision Plan Flexible Spending Accounts (FSAs) Health Care FSA Dependent Care… more
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