- Medtronic (North Haven, CT)
- …alleviate pain, restore health, and extend life for patients around the world. As a Regulatory Affairs Specialist , you will play a vital role in supporting ... with strong organizational skills. + Knowledge of document control systems and regulatory submission tools + Regulatory Affairs Certification (RAC-Devices)… more
- Medtronic (North Haven, CT)
- …in a more connected, compassionate world. **A Day in the Life** As a **Principal Regulatory Affairs Specialist ** at Medtronic, you will play a critical role ... **Nice to Have: Preferred Qualifications** + 7+ years of medical device regulatory affairs with roles showing increasing responsibility. + Strong leadership… more
- Bausch + Lomb (Hartford, CT)
- …degree or equivalent; Master's degree preferred + Minimum of 8 years in Regulatory Affairs with experience in the consumer product (Rx/OTC, OTC Monograph, ... Strong business acumen and ability to see the business drivers outside of Regulatory Affairs + Ability to take innovative ideas to promote a successful … more
- Bausch + Lomb (Hartford, CT)
- …Bachelor degree or equivalent, Master degree preferred + Minimum of 8 years in Regulatory Affairs or relevant experience in a regulated environment + Ability to ... Strong business acumen and ability to see the business drivers outside of Regulatory Affairs + Ability to take innovative ideas to promote a successful … more
- Medtronic (North Haven, CT)
- …for released surgical products, collaborating across departments such as R&D, Quality, Regulatory Affairs , and Marketing. You'll help drive effective execution ... the Life** Join Medtronic's Surgical Operating Unit as a Sr PD PMO Specialist in our Robotic Surgical Technologies (RST) Released Product Management (RPM) Project… more
- M&T Bank (Bridgeport, CT)
- …Risk, and internal partners such as the Risk Division, Internal Audit, and Regulatory Affairs . + Work is accomplished with periodic direction. The position ... programs that informs how to align practices with business objectives and regulatory requirements, including (but not limited to) developing complex process maps,… more
- Boehringer Ingelheim (Ridgefield, CT)
- …of required trial documents, contracts and necessary approvals + All Regulatory Requirements are satisfied prior to trial/site initiation + Where necessary, ... for CRAs, investigators and site staff + In collaboration with Trial Resource Specialist and with support from CRAs as appropriate, ensures collection of required… more
- Boehringer Ingelheim (Ridgefield, CT)
- …and facilitation skills. + Strong track record of interactions with regulatory affairs authority, international societies and other relevant stakeholders. ... of Concept studies), ideally clinical specialization hematology, oncology or organ specialist . Solid relationships with key stakeholders. + Sound medical and… more
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