5 часов назад
Senior Manager, R&D Product Development (Medical Devices)
149 700 - 213 200$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Senior Manager, R&D Product Development (Medical Devices): Leading the development of regulated medical devices and homeopathic products from concept through design transfer and commercialization with an accent on formulation, verification and validation, quality systems, and regulatory compliance. Focus on managing product development programs, scaling products for manufacturing, identifying technical and regulatory risks, and coordinating cross-functional execution.
Location: Hybrid in Princeton, New Jersey, USA; in-person attendance is required on Tuesdays, Wednesdays, and Thursdays, with remote work available on Mondays and Fridays.
Salary: $149,700–$213,200 per year, plus bonus eligibility.
Company
Church & Dwight develops consumer products, including regulated medical device and homeopathic product categories.
What you will do
- Lead workload management, project execution, and prioritization across medical device and homeopathic product development programs.
- Supervise, mentor, and support the performance and development of R&D team members.
- Develop the R&D portfolio and innovation pipeline in support of business growth, regulatory compliance, and global expansion.
- Lead collaboration with Regulatory, Quality, Clinical, Marketing, Operations, and Manufacturing functions.
- Manage product development from concept through design transfer, pilot-scale work, manufacturing scale-up, and commercialization.
- Support budgeting, resource planning, technical strategy, and risk mitigation.
Requirements
- Bachelor’s degree in Chemistry, Chemical Engineering, or a related discipline.
- 10+ years of laboratory experience, or a Ph.D. with 7+ years of experience.
- Experience with product quality, safety, compliance, and regulated product development.
- Ability to work in the Princeton hybrid schedule with in-person attendance three days per week.
- Experience with Design Controls, ISO 13485, FDA/cGMP, Design History Files, specifications, and technical reports.
Nice to have
- 5+ years of supervisory or management experience.
- Experience interacting with regulatory bodies, suppliers, or professional organizations.
Culture & Benefits
- Collaborative and supportive work environment with emphasis on ownership, innovation, and responsibility.
- Medical, dental, vision, and basic life insurance.
- Paid vacation, sick time, parental leave, paid holidays, and floating holidays.
- 401(k) plan with company match and profit-sharing.
- Discounted employee stock purchase plan.
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