- Gilead Sciences, Inc. (Foster City, CA)
- …review, approval and execution of all launch communication materials in advance of FDA filing and potential approach, such as press materials, HCP and patient ... storytelling, executive training and talking points, paid partnerships. + Oversee creation, training and briefing materials for key Gilead leaders, spokespeople and third-party voices. + Advance integrated activation of paid, earned, owned and social… more
- Bristol Myers Squibb (Summit, NJ)
- …accountable for driving operational excellence, ensuring compliance with all regulatory requirements ( FDA , DEA, DOT, ISBT, CTPAT, OSHA, VAWD, cGMPs), and fostering a ... culture of safety, collaboration, innovation, and continuous improvement. **Shift Available:** + Wednesday - Saturday (with e/o Wednesday off), Onsite Overnight Shift, 5 pm - 5:30 am **Responsibilities:** + Lead Cryopreservation and handling of all Cell… more
- Bristol Myers Squibb (Devens, MA)
- …experience in a regulated industry with 1+ year experience. Experience in FDA /EMA regulations in biopharmaceuticals or cell therapy manufacturing is preferred. + ... Demonstrated experience with electronic validation documentation systems. 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… more
- Aerotek (Danvers, MA)
- …safety rules, manufacturing procedures, company policies and procedures, QSR, and FDA regulations. **Essential Skills** + Attention to detail and hand dexterity. ... + Ability to learn and be trained on new skills and equipment. + Experience with cleanroom environments, medical device assembly, or manufacturing is preferred. + Microscope experience is preferred. **Additional Skills & Qualifications** + Good hand-eye… more
- Eurofins US Network (Norwood, MA)
- …and Ion Chromatography** + **Regulatory Knowledge:** Deep understanding of **CPSC, FDA , USP** , and environmental standards like **PFAS** regulations. **Additional ... Information** **Compensation:** + Salary: $100k-$150k **What we offer:** + Excellent full time benefits including comprehensive medical coverage, dental, and vision options + Life and disability insurance + 401(k) with company match + Paid vacation and… more
- J&J Family of Companies (Titusville, NJ)
- …drug development. + Experience using structured benefit-risk frameworks (eg, FDA benefit-risk framework, BRAT, PrOACT-URL) and/or experience with patient preference ... studies (eg, discrete choice experiments, best-worst scaling, threshold technique). + Experience leading projects with multi-stakeholder teams (eg, clinical, statistics, regulatory) on technical projects. + Experience presenting technical topics to… more
- Globus Medical, Inc. (TX)
- …with all company policies & procedures and maintaining compliance with US FDA and international medical device regulations and ISO 13485 quality system requirements. ... Participate in and provide support for customer phone inquiries, technical questions, and the documentation of all customer reports complaints / problems to ensure that customers are satisfied, and their needs are fulfilled. The job requires the individual to… more
- Owens & Minor (Springfield, MA)
- …Driver Training Program + Meet job-related requirements to comply with FDA and Joint Commissions regulations **SKILLS, KNOWLEDGE AND ABILITIES** + Patient ... Focused + Problem Solving/Analysis + Effective Communication + Integrity/Personal Credibility **Computer Skills** + Basic computer skills **Language Skills** + English (reading, writing, verbal) **Mathematical Skills** + Basic math skills **PHYSICAL DEMANDS**… more
- Medtronic (Minneapolis, MN)
- …leading cross-functional quality projects. + Strong knowledge of quality systems (eg, FDA regulations, ISO 13485). + Proficiency in root cause analysis tools (eg, ... Fishbone Diagram, 5 Whys). + Expertise in project management methodologies and tools. + Excellent communication, analytical and problem-solving skills. + Certified Quality Engineer (CQE) or Project Management Professional (PMP) certification. **Physical Job… more
- dsm-firmenich (Schenectady, NY)
- …skills + At least one-year prior manufacturing working experience preferred + Due to FDA safety and health requirements, the position does not allow for facial hair ... or artificial nails, also, the position requires the ability to wear PPE (personal protective equipment) including a respirator, consistently throughout the shift **About dsm-firmenich** At dsm-firmenich, we don't just meet expectations - we go beyond them.… more