- FleishmanHillard (San Francisco, CA)
- …field; Master's a plus. + Working knowledge of healthcare compliance requirements (eg, FDA , HIPAA, OPDP). + Strong grasp of digital measurement frameworks and how to ... connect performance data to storytelling impact. + A creative, strategic, and analytical mindset with a passion for health equity, innovation, and digital transformation. **Our Story** We're more motivated by what we can give than what we receive. That holds… more
- University of Southern California (San Diego, CA)
- …experience is required + Thorough understanding of records management requirements in FDA regulated trials + Ability to build and maintain positive relationships ... with management and peers and able to work successfully in a team environment + Excellent organizational and planning skills, including strong attention to detail + Excellent written and verbal skills required + Display strong analytical and problem-solving… more
- Abbott (Alameda, CA)
- …action system. + The incumbent also has a significant interaction with FDA / ISO during inspections. **Required Qualifications** + Bachelor's or Master's degree ... in Engineering, Life Sciences, Regulatory Affairs or a related field or equivalent combination of education and work experience. + Minimum 8 years of Quality experience in medical devices or pharmaceutical regulated environment. + Minimum 3 years… more
- Cedars-Sinai (Los Angeles, CA)
- …with 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. + Participates in required training and education programs. **Qualifications** **Qualifications:** + Bachelor's Degree preferred.… more
- Abbott (Alameda, CA)
- …+ Serve as a support during external audits (eg, Notified Bodies, FDA , Corporate), including logistics, documentation, and auditee coaching. + Monitor and ensure ... compliance with applicable regulatory standards applicable to ADC (ISO 13485, MDSAP, 21 CFR Part 820, etc.). + Maintain audit schedules, records, and metrics; track and trend audit findings to identify systemic issues. + Collaborate with cross-functional teams… more
- Abbott (Ontario, CA)
- …developments + 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 + Performs other related duties and responsibilities, on occasion, as assigned **Required… more
- Abbott (San Diego, CA)
- …regulations (ISO 13485, ISO 14971, IEC 62304, 21 CFR part 820.30-Design Controls, FDA SW Guidelines ). + Experience in delivering products for the Medical Device ... IVD industry. + Experience with testing techniques for cloud solutions. + Strong written, verbal, interpersonal and presentation skills. + Good understanding of the TLS\HTTPS REST\SOAP protocols. **Learn more about our health and wellness benefits, which… more
- Abbott (Temecula, CA)
- …device industry. + Knowledge of plastics processes, resins, tooling required. Knowledge of FDA QSR's and ISO requirements preferred. **WHAT WE OFFER :** At Abbott, ... you can have a good job that can grow into a great career. We offer: + A fast-paced work environment where your safety is our priority + Training and career development, with onboarding programs for new employees and tuition assistance + Financial security… more
- Sutter Health (Sunnyvale, CA)
- …Services (DHS), Drug Enforcement Administration (DEA), Food and Drug Administration ( FDA ) and the United States Pharmacopeia (USP) organization. Possess solid ... written and verbal communications skills to explain medical information clearly and professionally to diverse audiences, including patients, care givers, and families. Attention to detail when verifying medication identification and dosages, patient… more
- Bio-Techne (San Jose, CA)
- …environment Working knowledge of python programming language Understanding of GAMP5, FDA , and ISO regulations preferred. **Why Join Bio-Techne:** **We offer ... competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.** **We invest in our employees' financial futures through 401k plans, an employee stock purchase plan… more