Global Regulatory Affairs Lead (Medical Devices) - Hybrid
West Pharmaceutical Services
West Pharmaceutical Services is hiring a Principal Specialist in Regulatory Affairs in Exton, PA. This hybrid position focuses on developing and implementing regulatory strategies to ensure global approvals for medical devices, while mentoring team members. Ideal applicants should possess a Bachelor's degree and a minimum of 8 years of regulatory experience. Benefits include generous PTO, global career opportunities, and a collaborative culture that values diversity. #J-18808-Ljbffr West Pharmaceutical Services
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Senior Director, Global Quality & Regulatory Location: Exton, PA/USA We’re building... ...Define and lead the global Quality & Regulatory... ...regulatory requirements governing medical devices, biomaterials, and related... ...and/or Regulatory Affairs, preferably within medical...Medical device$110k - $135k
212° Titans is seeking a Lead Global Payroll professional to oversee payroll processing across multiple countries for approximately 500... ...position offers a competitive salary range of $110K-$135K and a hybrid work schedule, fostering both collaboration and flexibility....- GlaxoSmithKline is seeking a Regulatory Affairs Specialist to lead the planning and compilation of regulatory registration requirements. This hybrid position based in Upper Providence, Delaware... ..., involves collaborating with global submission teams and ensuring timely...
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...Senior Director, Global Strategy and Program... ...) and strategic lead for assigned tumor... ...together development, regulatory, medical, commercial, and... ..., Medical Affairs, Regulatory, Commercial... ...pharmaceutical, or medical device industry,... ...flexible, trust‑based hybrid working model for...Medical deviceWork at officeLocal areaFlexible hours3 days per week- This is a hybrid position requiring the team member to... ...with technical leads to targeted timelines in... ...single workstreams locally/globally and may work across multiple... ...their pharmaceutical/devices and general knowledge... ...managing projects in the medical device and pharma...Medical deviceWork experience placementLocal areaRelocationFlexible hours3 days per week
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$124k - $199.8k
...excellent working relationships with all internal business associates leading to a high level of customer satisfaction. Builds strong... ...selected candidate’s qualifications. Location This role will have a Hybrid Work arrangement, with the expectation of working in one of the...Temporary workWork at office3 days per week- ...degree in Accounting or Finance and at least 5 years of relevant experience. The position supports a hybrid work model, emphasizing collaboration for 3 days in the office per week and offers the chance to work on impactful projects within a global team. #J-18808-Ljbffr GHDWork at office
- ...delivery of contract regulatory services. You will... ...with evolving global regulatory expectations... ...Responsibilities Lead the development,... ...with Regulatory Affairs, Quality Assurance... ...skills. Experience in medical device regulatory affairs... .... This is a hybrid position requiring...Medical deviceContract workWork experience placementLocal area3 days per week
- ...an Analytical Lab, Project Analyst in a hybrid role based in the United States. The position... .... You will collaborate with technical leads and cross-functional teams to ensure... ...and experience in the pharmaceutical or medical device #J-18808-Ljbffr West Pharmaceutical ServicesMedical device
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