$137,000.00 - $235,750.00; not specified; not spec...
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Formulation development
Biosurgery product development
Medical device chemistry
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Johnson & Johnson is seeking an Associate Director of Formulation Chemistry in their Biosurgery MedTech division, located in Raritan, New Jersey. The role requires leadership in developing innovative surgical solutions through a multidisciplinary team, emphasizing regulatory compliance, product development, and team management.
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Job Summary
Lead and grow a multidisciplinary team of chemists and chemical engineers in Biosurgery R&D, overseeing resource deployment for new product development and lifecycle improvement projects.
Provide scientific and technical direction for formulation development, including polymer/biopolymer chemistries, adhesives, and hydrogels, ensuring optimization for functional performance, stability, and manufacturability.
Collaborate closely with cross-functional partners and represent the formulation function in leadership meetings, reporting project status, technical risks, and mitigation plans.
Matching Summary
Match Score: 75
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Johnson & Johnson is seeking an Associate Director of Formulation Chemistry in their Biosurgery MedTech division, located in Raritan, New Jersey. The role requires leadership in developing innovative surgical solutions through a multidisciplinary team, emphasizing regulatory compliance, product development, and team management.
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Salary
$137,000.00 - $235,750.00; Not specified; Not specified
Skills & Requirements
Must-have
formulation development
biosurgery product development
medical device chemistry
polymer/biopolymer chemistry
regulatory compliance for medical devices
Nice-to-have
people leadership
cross-functional collaboration
continuous improvement culture
innovation and scientific direction
Key Requirements
MS or PhD in Chemistry, Chemical Engineering, Materials Science, or related discipline
6+ years (PhD) or 8+ years (MS/BS) progressive industry experience in formulation development and leadership
Demonstrated experience leading teams and managing technical resources
Strong working knowledge of regulatory requirements for medical devices
Track record of successful technology transfer and scale-up