- BD (Becton, Dickinson and Company) (Salt Lake City, UT)
- …skills. **Preferred Skills:** + PMP certification or equivalent. + Knowledge of global regulatory (FDA, Anvisa, NMPA, MDR) and quality requirements (ISO, ... makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the...possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve.… more
- BD (Becton, Dickinson and Company) (Salt Lake City, UT)
- …Class II and III new medical device products in the market. + Knowledge of global regulatory (FDA, Anvisa, NMPA, MDR) and quality requirements (ISO, GB, JISC ... makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the...possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve.… more
- Merck (North Wales, PA)
- …Role in medical/legal/ compliance (CRT) reviews + Understanding of the US and Global regulatory stages and requirements + Job Owner - Fully responsible ... **Job Description** Our Company's Global Human Health Division abides by a "patient...& Disease learning resources for both the US and Global markets to ensure the knowledge, readiness and confidence… more
- BD (Becton, Dickinson and Company) (Salt Lake City, UT)
- …from concept through launch + PMP certification or equivalent + Knowledge of global regulatory requirements (FDA, Anvisa, NMPA, MDR) and quality standards (ISO, ... makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the...possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve.… more
- BeOne Medicines (Emeryville, CA)
- …and/or health economic and outcomes research in the oncology space + Familiarity with global regulatory and medical affairs environments (eg, US, EU, APAC) + ... Writer to lead the tactical execution of publications stemming from our global medical affairs publication plans. These plans span across early phase development… more
- Gilead Sciences, Inc. (Foster City, CA)
- …trials are conducted in compliance with Gilead procedures, GCP and applicable global regulations + Analyze trends to identify process gaps, improvement opportunities ... and CAPA management team within Gilead R&D Quality on internal audits, regulatory agency inspections, risk assessment, deviations and CAPA activities + Liaison and… more
- Raymond James Financial, Inc. (St. Petersburg, FL)
- Define and establish delivery plans for complex global enterprise technology projects. Evaluate multi-faceted project requests for technical feasibility & ... of technical & business SMEs to deliver Banking, Finance and Regulatory technology projects while driving continuous improvement to project management methodologies.… more
- Bristol Myers Squibb (Princeton, NJ)
- …of work + Ensure that all marketing activities are compliant with regulatory and legal requirements **Qualifications:** + Bachelor's degree with minimum 5 years ... environment + Ability to successfully navigate internal MLR (medical, legal, regulatory ) review processes + Demonstrated project management experience + Demonstrated… more
- Bristol Myers Squibb (Seattle, WA)
- …data governance, security, and compliance with internal and external regulatory requirements.** + **Troubleshoot data-related issues and implement solutions to ... (eg, Snowflake, Redshift).** + **Familiarity with GMP data requirements and regulatory expectations for data integrity.** + **Proven ability to work… more
- BeOne Medicines (Pennington, NJ)
- …Lead investigations and resolve complex manufacturing issues. + Manage and coordinate global change ensuring stakeholders alignment. Assist in Regulatory filings ... data and metrics driven culture. Relentlessly maintain alignment with other global manufacturing sites through shared knowledge, shared manufacturing data, shared… more