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• Irvine
• US$110000 - US$120000.00 per annum
• Posted 18 days ago

JOB SUMMARY This position is responsible for manufacturing quality operation activities including, but not limited to, management of process improvements, verification and validation efforts, reliability testing, support of Quality Control inspection and testing, data analyses and trending and mo...

• Irvine
• US$110000.00 - US$120000.00 per annum
• Posted 18 days ago

JOB TITLE: Senior Supplier Quality Engineer DEPARTMENT: Quality Assurance REPORTS TO: Quality Director JOB SUMMARY In this role, the Senior Supplier Quality Engineer provides quality leadership and governance to our medical device supplier management program. This role leads the selection and qua...

• New Jersey
• US$350000 - US$400000 per annum
• Posted 18 days ago

Vice President, Global Regulatory Affairs New Jersey - United States Seeking a proven leader to join a small Regulatory team as VP of Regulatory Affairs to drive the reg strategy development plans for Cell and Gene Therapy programs while overseeing and supporting the growing global regulatory tea...

• Cranbury
• Up to US$0.00 per annum + DOE
• Posted 18 days ago

Director, Global Regulatory Affairs Remote - United States Seeking a proven leader to join a small Regulatory team as VP of Regulatory Affairs to drive the reg strategy development plans for Cell and Gene Therapy programs while overseeing and supporting the growing global regulatory team and all ...

• Delaware
• DOE
• Posted 18 days ago

Manager/Senior Manager, Global Regulatory CMC Delaware - United States (relocation assistance provided) Seeking a highly experienced and driven Regulatory CMC leading professional to join a small group within a very established biotech-setting. We are looking for a highly qualified and confident ...

• Wilmington
• US$175000 - US$185000 per annum
• Posted 18 days ago

Associate Director, Global Regulatory CMC Delaware - United States Seeking a highly experienced and driven Regulatory CMC leading professional to join a small group within a very established biotech-setting. We are looking for a highly qualified and confident CMC leading subject matter expert to ...

• Irvine
• US$60000 - US$85000 per annum
• Posted 19 days ago

Complaint Investigation Specialist Job Responsibilities: Performs technical product investigations associated with complaints, collaborating with R&D Engineers, Manufacturing Engineers, Quality Engineers and Clinical, when necessary. Documents and codes device analysis and failure investigation r...

• Carlsbad
• US$140000 - US$155000.00 per annum + bonus, benefits, hybrid work
• Posted 23 days ago

We are hiring a Regulatory Affairs Manager (NO prior Management expeirence required) to work hybrid on-site at our location in San Diego, California. This role will be responsible for preparing domestic and international regulatory strategies and submissions for our Software and Imaging technolog...

• Carlsbad
• US$110000 - US$135000.00 per annum + bonus, benefits, hybrid work
• Posted 23 days ago

We are hiring a Regulatory Affairs Specialist OR Senior Regulatory Affairs Specialist to work on-site at our location in San Diego, California. This role will be responsible for preparing domestic and international regulatory strategies and submissions as well as the support of daily activities r...

• San Diego
• Up to US$220000.00 per annum + bonus, benefits
• Posted 24 days ago

The Regulatory Affairs Director will build and lead a growing Regulatory Affairs team by recruiting, managing, coaching, and developing the team to ensure skills are aligned with a high-performing organization. This position will direct the Regulatory team in supporting products over their lifecy...

• Cranbury
• Up to US$0.00 per annum + DOE
• Posted 24 days ago

Director, Global Regulatory CMC New Jersey - United States Seeking a proven leader to join a small Regulatory team as Director of Regulatory CMC to drive the reg strategy development plans for Cell and Gene Therapy programs while overseeing and supporting the growing global regulatory CMC team an...

• Redwood City
• Up to US$9 per annum + DOE
• Posted 24 days ago

Associate Director, Medical Writing Remote - United States Seeking an experienced Associate Director of Medical Writing to provide guidance, leadership, and expertise to the project teams and outside vendors, and external contacts. This position is responsible for writing, editing, and coordinati...