- Barry Callebaut (American Canyon, CA)
- …accountability, and teamwork. Regulatory Compliance * Ensure compliance with OSHA, FDA , USDA, EPA, and other regulatory bodies. * Participate in internal ... and external audits, inspections, and certification processes. * Maintain updated records of cleaning activities, chemical usage, and validations. Quality Control & Inspections * Conduct regular inspections of production lines, equipment, and common areas. *… more
- BD (Becton, Dickinson and Company) (Irvine, CA)
- …of regulatory requirements and quality standards in the medical device industry ( FDA , ISO 13485, ISO 60601) + Excellent problem-solving skills and ability to ... work effectively in a fast-paced, collaborative environment + Strong communication and interpersonal skills, with ability to convey technical information to non-technical stakeholders + Experience with requirement management tools (PTC, JAMA, or DOORS) +… more
- BeOne Medicines (San Mateo, CA)
- …(eg, clinical development, medical, regulatory, labeling) and external stakeholders (eg FDA , MHRA, EMA, other regulatory agencies) + Contribute to continuous ... employee development programs, such as mentoring, coaching, and peer-to-peer learning + Contribute to and provide Safety Science training to support team development + Demonstrate knowledge and application of pharmacovigilance principles to related tasks that… more
- Danaher Corporation (Lodi, CA)
- …for continuous improvement of OEE and maintenance processes for compliance with Company, FDA , ISO, OSHA and GMP regulations. The essential requirements of the job ... include: + High School degree with 8+ years of experience or bachelor's degree with 5+ years of related work experience + Hands-on equipment experience with hand tools and machine shop tooling expertise + Proficient in Word, Excel, PowerPoint, Outlook, and… more
- Imperative Care (Campbell, CA)
- …new solutions, and incorporate continuous improvements stemming from technology advancement, FDA feedback, and/or applicable standards What You'll Bring + Bachelor's ... degree in engineering, or related discipline and a minimum of 5 years of related experience or master's degree in engineering with 2 years of related experience in the medical device or related regulated industry; or equivalent combination of education and… more
- Abbott (Livermore, CA)
- …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. **Required Qualifications** + High School Diploma / GED or an equivalent combination of education and… more
- Danaher Corporation (Brea, CA)
- …in: + Experience with healthcare regulation, including: fraud and abuse (eg, anti-kickback); FDA for medical devices; data use and privacy (eg, HIPAA, GDPR); and ... anti-corruption (eg, FCPA) + Experience with software transactions The salary range for this role is $160,000-$190,000 annually. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting.… more
- VTI Life Sciences (San Diego, CA)
- …execution, and reporting is a plus. + Previous experience in a cGMP/ FDA -regulated manufacturing environment is a plus. + Must be proficient with/ Microsoft ... Office, including Word, Excel, PowerPoint, etc. + Must have technical writing, review, and analytical skills in addition to strong verbal communication and presentation skills + Must have a strong ability to organize and manage multiple tasks in a fast-paced… more
- Edwards Lifesciences (San Francisco, CA)
- …Our other star player? You! IHFM has achieved a significant milestone and received FDA approval for our Cordella PA Sensor. Join us as we commercialize this ... revolutionary heart failure management system! As the Area Sales Manager at IHFM, you will play a pioneering role in driving the adoption and growth. You will lead the charge in establishing IHFM's presence in **Northern California** within the healthcare… more
- Cedars-Sinai (Los Angeles, CA)
- …all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board. Maintains research practices using Good ... Clinical Practice (GCP) guidelines. Maintains strict patient confidentiality according to HIPAA regulations and applicable law + May serve as one point of contact for external sponsors for select trials. May respond to sponsor inquiries and attend meetings… more