- Ankura (Chicago, IL)
- …guidance; trade association guidance; and international compliance standards governing pharmaceutical and medical device operations. You will be joining a team ... with backgrounds in compliance, regulatory, legal, audit, operations, nursing, pharmacy, medical science, economics, accounting, and data science. As a Senior … more
- Edwards Lifesciences (Naperville, IL)
- …cath lab/OR environment and procedural best practices + Expert understanding of medical device asset creation, regulation requirements for claims and training ... **Sr. Director , Global Professional Education, Training - IHFM** Many...cross functional teams such as complaints, Engineering, regulatory affairs, quality affairs and clinical affairs + Regularly interacts with… more
- AbbVie (North Chicago, IL)
- …medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's ... Tok (https://www.tiktok.com/@abbvie) . Job Description The Pharma Product Group Associate Director will be fully accountable for providing CMC leadership and… more
- Guidehouse (Chicago, IL)
- …program design, implementation, and monitoring services to pharmaceutical, biotechnology, and medical device , companies. We support our clients across the ... multiple projects simultaneously of all varying sizes and durations to ensure quality control and key client's perceived value while supervising, mentoring and… more
- AbbVie (North Chicago, IL)
- …for Medical Devices or Combination Products. Assure that high quality products are manufactured in compliance with local and international regulations, and ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...Quality expectations. + Lead the development of ECM Device Financial Operating Plan, Updates, LRP, and Standard processes,… more
- Ankura (Chicago, IL)
- …and pharmacy benefit management companies, as well as pharmaceutical and medical device manufacturers. Responsibilities: + Applies clinical experience and ... counsel during internal and externally driven investigations through the evaluation of medical records, the determination of medical necessity and appropriate … more
- United Therapeutics (Springfield, IL)
- …), livers ( **miroliver(R)** ), and a bioengineered external liver assist device for acute liver failure ( **miroliver** **_ELAP_** **(R)** ), with plans ... of biologic or pharma regulatory experience with a Bachelor's Degree in life sciences, quality , regulatory affairs or a related area of study or 10+ years of… more
- Danaher Corporation (Richmond, IL)
- …with increasing responsibility in medical device /IVD + Experience working within a medical device quality system in compliance with US FDA, ISO 13485 ... nonconformance workflows, CDT&R, and calibration. This position reports to the Director , Quality Assurance and Regulatory Compliance responsible for ensuring… more
- PCI Pharma Services (Rockford, IL)
- …future of PCI. **Job Title: Senior Validation Engineer - Medical Device Assembly (CDMO)** **Location:** [Rockford] **Department:** Quality **Reports To:** ... **Senior Validation Engineer** to support the validation activities associated with medical device assembly lines within a fast-paced Contract Development… more
- Ghafari (Chicago, IL)
- **Job Description:** **General Summary** Under the direct supervision of the Director of Electrical Engineering or senior staff, the Electrical Engineer - Power ... and documenting power system studies, including short circuit analysis, protective device coordination, and arc flash hazard studies. The engineer will provide… more