- Danaher Corporation (Indianapolis, IN)
- …Life Science Products in multiple manufacturing locations. This position reports to the Sr . Manager , Global NPI Operations-Systems/Hardware and is part of the ... + Regulatory Knowledge: Experience implementing design changes in regulated environments ( FDA , ISO, Automotive) while meeting deadlines Travel, Motor Vehicle… more
- CBRE (Ridgefield, CT)
- …varied shifts. + Work under general supervision of the CBRE Sr . Account Manager at a GMP regulated facility maintaining FDA quality standards. + Document all ... High School Diploma, GED, or currently enrolled in a 2 or 4-year college program or technical school. + May require a valid driver's license. + Physical requirements… more
- Mallinckrodt Pharmaceuticals (Bridgewater, NJ)
- …vision & strategy. This role manages the enterprise's information security program , identifies, and evaluates IT and cybersecurity risks, and ensures the ... The CISO communicates the impact of cybersecurity on the business to senior stakeholders and ensures that information systems are secure and compliant with… more
- University of Colorado (Aurora, CO)
- …ensure compliance with requirements of the Food and Drug Administration ( FDA ), study protocols, department, hospital/clinical standard operating procedures and other ... Sponsor, Data Safety Monitoring, and Food and Drug Administration ( FDA ) audits and responses + Participate in subject recruitment...+ Act as a Primary Coordinator on multiple trials/studies ** Senior Level or CRC III, all the above and:**… more
- Bausch + Lomb (Tampa, FL)
- …health in the future. **Objectives/Purpose of Job:** As a Principal Engineer, Program /Project Manager , you will lead scope development, capital budget ... milestones. + Facilitate regular project status meetings, provide updates to senior leadership, and escalate issues with recommendations necessary to ensure timely… more
- Curia (Albuquerque, NM)
- …day of employment) + Career advancement opportunities + Education reimbursement + 401k program + Learning platform + And more! Summary: The Process Engineer IV will ... efficiency, and ensure compliance with industry standards such as cGMP and FDA regulations. Essential Duties and Responsibilities: + Develop batch records for… more
- CVS Health (Annapolis Junction, MD)
- …long term care facilities and to other customers in the healthcare environment. While senior care has long been an Omnicare specialty, we also serve other targeted ... Omnicare Pharmacy and will report directly to the General Manager . The PIC will work to develop and implement...and compliance developments (eg, state Board of Pharmacy, DEA, FDA , etc.) for pending regulatory changes and partner with… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …product lifecycle for all Olympus therapeutic areas. You will report directly to the Senior Director Medical Safety as a member of the global medical safety team. ... and experience working with: + Various regulations (HIPPA, EU-MDR, FDA 21 CFR Part 803, 806, 820) + Various...coverage effective on start date + 24/7 Employee Assistance Program + Free live and on-demand Wellbeing Programs +… more
- Bristol Myers Squibb (Devens, MA)
- …quality and compliance across Bristol Myers Squibb. As a trusted advisor to senior leadership, the VP ensures alignment with business goals and global regulations, ... will develop and sustain the QMS working collaboratively with senior leaders across R&D, GPDS and Commercial. + Oversees...in GxP environment. + Previous proven experience dealing with FDA and other major regulatory agencies. + Experience with… more
- University of Rochester (Rochester, NY)
- …adherence to agency guidelines. Work closely with Principal Investigator (PI) and lab manager 2-3 months prior to account close to avoid deficits and/or overages. + ... Prepare and review reports with Senior Accountant and Administrative Director before sending to investigator...T32 training grant, two U54 grants, and a large FDA contract. + Prepare annual final financial reports for… more