- Abbott (Alameda, CA)
- …. 5 years' experience working with Class II, Class III medical devices and/or biologics/drugs. Regulatory Affairs Certification (RAC) is a plus. ... regulatory submissions for Pharmaceutical, in vitro diagnostic devices and/or medical devices . ....device regulations and submissions. . Familiar with relevant regulatory requirements for medical devices … more
- J&J Family of Companies (Irvine, CA)
- …all relevant Clinical R&D partners and cross-functional partners (eg Global Strategic Marketing, Medical Affairs , Regulatory Affairs , Health Economics ... study team; o Cooperates with cross-functional teams (Research & Development, Complaint Handling, Quality/ Regulatory , Medical Affairs , Medical Safety) to… more
- J&J Family of Companies (Irvine, CA)
- …all relevant Clinical R&D partners and cross-functional partners (eg Global Strategic Marketing, Medical Affairs , Regulatory Affairs , Health Economics ... based on study need; + In EMEA, responsible for Regulatory Affairs related tasks associated with clinical...with budget planning, tracking and control is required. + Medical Device experience is required. + Sound… more
- AbbVie (Irvine, CA)
- …LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Senior Manager, Regulatory Affairs , Device works with internal and external ... factors testing, device risk analysis (ISO 14971) and other global regulatory requirements for Allergan's devices and combination products. This role is… more
- AbbVie (Irvine, CA)
- …to be a team leader and engage key stakeholders, including global strategic marketing, medical affairs , regulatory affairs , clinical development, and ... be to evaluate the interaction of current and future medical devices with cells and tissues for...methods to support development of novel medical device /tissue products. + Critically evaluate scientific or regulatory… more
- BeOne Medicines (Emeryville, CA)
- **General** **Description:** The Director, Regulatory Affairs , Dx/CDx and Medical Devices will be responsible for leading a small team for developing and ... implementing regulatory diagnostic and medical device ...externally with a solid background in medical devices /diagnostic development regulations and associated regulatory deliverables.… more
- Abbott (Santa Clara, CA)
- … device regulations and guidelines, and product and therapeutic area knowledge to support Regulatory Affairs medical device submissions in the EU for ... in clinical research, clinical affairs , regulatory affairs , or quality systems, in the medical device or pharmaceuticals industry. + 3-5+ years of… more
- BD (Becton, Dickinson and Company) (Milpitas, CA)
- …Preferred + RAC ( Regulatory Affairs Certification) a plus. + Medical Device Industry preferred - will consider other REGULATED Industry experience + ... focus on regulatory affairs . + 3+ years of related regulatory submission experience from a medical device and/or IVD industry. + Ability to work in a… more
- Abbott (Alameda, CA)
- …+ Experienced in regulatory submissions for Pharmaceutical, in vitro diagnostic devices and/or medical devices . + Experience of working within ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
- Abbott (Sylmar, CA)
- …in Mandarin + Previous regulatory compliance, R&D, and/or quality experience in medical device industry + Good working knowledge of the product development ... of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines....Sylmar, CA currently has an opportunity for a Senior Regulatory Affairs Specialist-China. As a Senior … more