On Site Jobs
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Regualtory Affairs Specialist
Regulatory Affairs SpecialistMedical Device / Pharma | Hybrid Opportunity | Competitive Salary + BenefitsAre you a Regulatory Affairs professional looking for an opportunity to make a real impact on innovative products that improve patient outcomes?A growing healthcare organisation is seeking a Regulatory Affairs Specialist to join its expanding te...
Senior Director of Quality
Role: Senior Director of QualityLocation: South San Francisco, CA (On-site)Salary: $190,000 - $250,000EPM is partnered with a rapidly scaling, mid-sized medical device company operating at the forefront of surgical robotics innovation. This organization has established itself as a leader in advanced robotic-assisted technologies designed to improve...
Talent Pipeline Midwest Dermatology Reps
Dermatology Sales Specialist - NortheastI'm looking for standout Dermatology sales talent across the Northeast. OverviewWe are partnering with a growing pharmaceutical organization launching their dermatology portfolio across the Northeast. This is a unique opportunity to join at the ground level of a buildout, with strong visibility, career growth...
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Talent Pipeline West Dermatology Reps
Dermatology Sales Specialist - WestI'm looking for standout Dermatology sales talent across the West. OverviewWe are partnering with a growing pharmaceutical organization launching their dermatology portfolio across the West. This is a unique opportunity to join at the ground level of a buildout, with strong visibility, career growth, and the abili...
Sr. Quality Engineer
Position SummaryWe are seeking a Senior Quality Engineer to support quality initiatives across product development, manufacturing, and post-market activities for a growing medical device organization. This individual will partner with cross-functional teams to ensure products consistently meet quality, regulatory, and customer requirements while dr...
Senior Manager Regulatory CMC
Senior Manager, Regulatory CMCThe Senior Manager, Regulatory CMC is responsible for supporting global regulatory chemistry, manufacturing, and controls (CMC) activities with an emphasis on lifecycle management, post-approval changes, and regulatory compliance. This role partners closely with cross-functional teams to develop and execute regulatory ...
