- Sokol Materials & Services (Skillman, NJ)
- …experience in CQV and/or CSV within the pharmaceutical, biotechnology, cell therapy or medical device industries. + Experience with Cell Therapy equipment (cell ... guidelines, industry trends, and best practices related to validation and quality assurance. Industry Awareness: Stay up-to-date with regulatory guidelines,… more
- Merck (Rahway, NJ)
- …test primary and secondary packaging components + Demonstrated understanding of Medical Device and Combination Product regulations + Demonstrated understanding ... areas of Pharmaceutical new product development **Preferred Experience and Skills:** + Medical Device and Combination Product Packaging development experience + … more
- Fujifilm (Trenton, NJ)
- …II + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... and other Key Operators in the use of Fujifilm's Medical Informatics. The Senior Clinical Consultant, MI - I...HCUS's future business activities. + Adheres to the Company's quality and regulatory compliance requirements and ensures… more
- Fujifilm (Trenton, NJ)
- …I. + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... and other Key Operators in the use of Fujifilm's Medical Informatics. The resource will assist with the development...HCUS's future business activities. + Adheres to the Company's quality and regulatory compliance requirements and ensures… more
- RWJBarnabas Health (New Brunswick, NJ)
- …Functions: * Administer aerosol medication, Chest PT and related therapies including medical gas therapy per physician orders or approved protocols. Perform rounds ... specific needs identified. Evaluate therapy orders for completeness, appropriateness, quality and effectiveness using Evidence-Based Practice Guidelines. Recommend changes… more
- Bristol Myers Squibb (Princeton, NJ)
- …of industry experience in bioanalysis and/or IVD/CDx development within pharmaceutical, biotech, medical device , or CRO settings. + Direct experience managing ... quality teams. **Cross-Functional Coordination** + Work collaboratively with scientific, technical, quality , regulatory , IT, finance, and legal teams to drive… more
- Fujifilm (Trenton, NJ)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... with a Master's degree. + Minimum 8 years of medical device industry experience in a clinical...evolving situations and needs + Strong commitment to delivering high- quality work and upholding HCUS values. + Proficiency in… more
- Marotta Controls, Inc. (Montville, NJ)
- …Controls, a New Jersey Top Workplace three years running! Dedicated to innovation, quality and excellence, we deliver cutting edge control systems for the Aerospace ... you'll collaborate with our cross-functional production and engineering team to achieve quality and on-time delivery goals. By completing our optional on-site solder… more
- Sokol Materials & Services (Skillman, NJ)
- …interest in pursuing a career in CQV within the pharmaceutical, biotechnology, or medical device industries. + Excellent organizational skills and attention to ... programs and workshops to advance skills in validation and quality assurance. * Stay updated on regulatory ...and quality assurance. * Stay updated on regulatory guidelines, industry trends, and best practices in validation.… more
- Sokol Materials & Services (Skillman, NJ)
- …Minimum of 7 years of CQV experience in pharmaceutical, biotechnology, cell therapy, or medical device industries, with at least 5 years focused on utilities and ... qualification. + Strong understanding of validation principles, methodologies, and regulatory requirements, including FDA, EMA, and ICH guidelines. Knowledge, Skills… more