- Teva Pharmaceuticals (West Chester, PA)
- Manager , CMC Regulatory Affairs - Remote OR West Chester, PA Date: May 15, 2024 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva ... a difference with. **How you'll spend your day** As Manager , CMC Regulatory Affairs you will be...as with internal regulatory departments, provide for support cross functional product teams for CMC specific projects and may… more
- Teva Pharmaceuticals (West Chester, PA)
- … Manager , Manager & Associate III). The Sr Director, Regulatory Affairs CMC is responsible for identifying and evaluating CMC issues associated with product ... network, as well as with internal regulatory departments. The Sr Director, Regulatory Affairs CMC will oversee cross functional product teams for CMC specific… more
- Pfizer (Collegeville, PA)
- …plans. + Prior experience in working in Medical Affairs /clinical affairs is highly desired. + Cross functional effectiveness: Ability to effectively ... **ROLE SUMMARY** The Vaccines Operational Excellence Sr. Manager is an integral member of the Global & US Medical Affairs Teams, and the Operational & Change… more
- Pfizer (Collegeville, PA)
- …our business: You will: + Partner with brand teams and corporate affairs across Pfizer's commercial organization to develop strategies and activations for earned ... of modern earned media strategies + Sit with cross functional teams to activate earned media plans across key...specific to therapeutic areas + Partner with our corporate affairs team, media planning team and brand teams to… more
- Pfizer (Collegeville, PA)
- …Team members (eg Regulatory strategy leads, Safety Risk Lead, Clinical Development, Medical , and other cross- functional SMEs) + GLLs partner with Labeling ... for Labeling Team members (eg Regulatory Strategist, Safety Risk Lead, Functional Line SMEs, Labeling Justification Document/Clinical Overview author) and will… more
- Pfizer (Collegeville, PA)
- The Labeling Operations Manager (LOM) provides operational support for the initial creation and relevant updates to labeling documents including the Core Data Sheets ... and their associated Patient Labeling Documents. The Labeling Operations Manager , Senior Manager is capable of managing...serve as a mentor. + Facilitate team and cross functional meetings. + Contribute to the development of continuous… more
- Organon & Co. (Plymouth Meeting, PA)
- …years of industry experience in R&D functions (eg, Clinical Research, Early Development, Medical Affairs , Pharmacovigilance, Regulatory Affairs , etc.). + At ... drugs or devices which improve human health. The Program Manager may also be assigned to projects that contribute...in a team setting as a leader, chair, or functional contributor. + Demonstrated ability to manage one or… more
- ATS Automation (Warminster, PA)
- …compliance with industry standards and regulations. + Collaborate with cross- functional teams, including R&D, manufacturing, quality assurance, and regulatory ... affairs , to ensure seamless integration of mechanical systems into...experience in mechanical engineering roles within the pharmaceutical or medical device industry, with a focus on equipment design… more