- Olympus Corporation of the Americas (Center Valley, PA)
- …Manufacturing is responsible for managing the onboarding manufacturers of sourced finished medical device products to ensure products meet current Good ... Manufacturing Practices, applicable medical device regulatory requirements, and for supporting business development initiatives. **Job Duties** + Supports… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …of 6 years of experience. + Prior experience in a sponsor, CRO, or medical device company. In-depth knowledge and experience with FDA regulations and familiarity ... and GCDMP. + Strong expertise in implementing and maintaining systems for global medical device trials (Class II/III or combination products). + Excellent… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …guidance of the Clinical Research Associate (CRA), Data Management and/or the Clinical Project Manager to ensure compliance with specified study protocols. + ... (Sr. CTC) will be responsible for supporting the clinical project team during all stages of a clinical study...(2) or more years experience in clinical research, with medical device and/or pharmaceutical trials. + Strong… more
- Envista Holdings Corporation (Quakertown, PA)
- …operations, regulatory and quality backgrounds that work collaboratively in the fast-paced medical device field. A friendly and open atmosphere helps to ... facing tools that are on time, within specification and cost in the regulated medical device industry. The position is responsible for the tactical planning and… more
- Envista Holdings Corporation (Quakertown, PA)
- …operations, regulatory and quality backgrounds that work collaboratively in the fast-paced medical device field. A friendly and open atmosphere helps to ... software. + Performs other duties and tasks as assigned by their supervisor/ manager . **Most Important Competencies Required** + Diplomacy/Teamwork - Easy to work… more
