- Hologic (San Diego, CA)
- …Report any potential quality or regulatory issues to the Global Supplier Quality Sr. Director / Director that may affect product quality or ... auditing program, ensuring that our suppliers adhere to rigorous regulatory and quality standards. You will lead...Performance Indicators. + **Support Leadership:** Assist the Global Supplier Quality Sr. Director / Director as needed.… more
- GRAIL (Menlo Park, CA)
- … Quality , Lab Operations, and other stakeholders to support regulatory strategy development, product validation, audits, promotional material review, on-market ... Requirements:** + **Experience** + Minimum of 8 years of experience in regulatory , development, clinical affairs, quality , or program management within the… more
- United Therapeutics (Sacramento, CA)
- …of biologic or pharma regulatory experience with a Bachelor's Degree in life sciences, quality , regulatory affairs or a related area of study or 10+ years of ... or pharma regulatory experience with a Master's Degree in life sciences, quality , regulatory affairs or a related area of study or 7+ years of biologic or… more
- Gilead Sciences, Inc. (Foster City, CA)
- …+ Provides regulatory impact assessments for changes managed in the quality systems and participates in technical risk assessment exercises. + Coaches and ... illnesses worldwide. **Responsibilities** + Responsible for leading all CMC regulatory activities for assigned project(s), in line with ICH requirements,… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Description** . **Strategic Leadership & Vision** Define and drive global regulatory strategies for combination products, ensuring alignment with corporate goals and ... regulatory expectations. Champion regulatory innovation and novel approaches to accelerate development and approval timelines. Provide guidance to PDM Teams and… more
- Gilead Sciences, Inc. (Foster City, CA)
- …relevant experience. + BA/BS with 10+ years' relevant experience. + Significant regulatory , quality , compliance or related experience in the biopharma industry. ... create possible, together. **Job Description** You will act as the Regional Regulatory Lead on more complex or multiple products, compounds, indications or projects… more
- BeOne Medicines (San Mateo, CA)
- **_General Description:_** BeOne is seeking an experienced and energetic regulatory professional to manage, evaluate, and complete regulatory projects consistent ... responsible for development of strategies, planning, drafting, and managing CMC-related regulatory submissions and HA interactions to meet the aggressive timelines… more
- BD (Becton, Dickinson and Company) (Brea, CA)
- **Job Description Summary** The Director , Quality Engineering - WW IPD is responsible for developing and leading the global Design Center Quality function ... EMEA, the Director provides strategic leadership and technical support to Quality Engineering teams located in Brea, San Diego, and TCI. The role also… more
- Kelly Services (South San Francisco, CA)
- …cGMP-related activities to ensure our client's development programs meet regulatory and quality standards. Reporting to the Executive Director of Quality ... Kelly(R) Science & Clinical is seeking a Director of CMC Quality for a...treatment options. **Key Responsibilities** + Develop strategies aligning with regulatory standards for manufacturing high- quality clinical supplies… more
- Stanford Health Care (Palo Alto, CA)
- …clinical quality and standards. The Director will collaborate with quality management and external regulatory and accrediting entities to ensure all ... Day - 08 Hour (United States of America) This Director will have oversight of both the Adults and...and goals of SHC and which meet the external regulatory and statutory requirements. + Effectively assists in providing… more