- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- …have as well as a demonstrated knowledge of drug/ device combination and medical device products and their regulatory pathways. + Demonstrated Quality ... Collaborates with other external functions on CMC matters (eg, Quality, Commercial, Regulatory Affairs , etc.). Ensures the CMC function is adequately represented… more
- BD (Becton, Dickinson and Company) (Vernon Hills, IL)
- …surgery-specific medical device experience) + Strong expertise in medical affairs , KOL engagement, and the clinical/ regulatory landscape specific ... on medical strategy and key objectives with cross-functional partners, including medical , clinical, commercial, regulatory , R&D, and market access teams. +… more
- PCI Pharma Services (Rockford, IL)
- …shape the future of PCI. **Job Title: Senior Validation Engineer - Medical Device Assembly (CDMO)** **Location:** [Rockford] **Department:** Quality **Reports ... **Senior Validation Engineer** to support the validation activities associated with medical device assembly lines within a fast-paced Contract Development… more
- Rush University Medical Center (Chicago, IL)
- **Job Description** Location: Chicago, Illinois Business Unit: Rush Medical Center Hospital: Rush University Medical Center Department: Pediatrics-Res Adm **Work ... Neurology Research will be responsible for the overall fiscal, regulatory , operational, administrative, and personnel management of the Pediatrics Neurology… more
- J&J Family of Companies (Chicago, IL)
- …and profoundly impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Medical Affairs Group **Job Sub** **Function:** Medical ... (CAS) partners with Level 2 or 3 CAS and Medical Affairs to learn training and certification...learn training and certification criteria for J&J Vision (JJV) Medical Devices . This includes our Refractive Laser… more
- Edwards Lifesciences (Chicago, IL)
- …Knowledge and understanding of Edwards policies, procedures, and international and domestic medical device regulatory guidelines relevant to clinical ... patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you… more
- AbbVie (North Chicago, IL)
- …course of our work, we collaborate with early-stage CMC, Quality Assurance, Regulatory Affairs , Internal and External Manufacturing, and other cross-functional ... + 10-12 years of experience (MS 8-10 years, PhD 2-4 years) ideally in the medical device , drug delivery or other regulated industry + Strong communication skills… more
- AbbVie (North Chicago, IL)
- …experience within one of the most dynamic organizations in the pharmaceutical and medical device industry. You will support the Internal Audit & Inspection ... research, business administration in a healthcare setting or auditing, regulatory affairs , or other related degree +...between December 2026 - June 2027 Preferred Qualifications + Medical device or project management experience Additional… more
- Abbott (Abbott Park, IL)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... Experience** + Associate's degree required + 7 years of Cath Lab and/or Medical Device experience **Preferred Experience** + Bachelor's Degree highly preferred.… more
- Exelon (Oakbrook Terrace, IL)
- …relationships with both internal and external stakeholders including, Engineering, Regulatory , Legal, Governmental Affairs , and unversities, national ... development and implementation of short and long term strategic initiatives. Support regulatory intiatives for new technology. (25%) + Manage the performance and… more