9 дней назад
Senior Manager, Drug Product Analytics
139 100 - 231 900$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Manager, Drug Product Analytics (Pharmaceutical Analytics): Leading analytical scientists and analytical strategies for Pfizer's small-molecule portfolio from early development through commercialization with an accent on control strategy, regulatory submissions, and cross-functional CMC delivery. Focus on developing and defending analytical strategies, overseeing CRO and CMO activities, coaching scientists, and implementing digital tools and new technologies.
Location: United States – Connecticut – Groton; on-premise work. Occasional travel may be required. Relocation support may be available.
Annual base salary: $139,100–$231,900, plus a 17.5% bonus target and eligibility for a share-based long-term incentive program.
Company
develops pharmaceutical products and supports drug development, manufacturing, regulatory, and commercial activities.
What you will do
- Lead, coach, and develop a team of Analytical Scientists.
- Direct analytical development and phase-appropriate control strategies for small-molecule programs from early development through commercialization.
- Serve as the analytical lead within multidisciplinary CMC teams and influence project strategy, risk management, and development decisions.
- Lead analytical contributions to regulatory submissions, including control strategies and responses to health authority questions.
- Oversee analytical work performed by CROs, CMOs, and external partners.
- Establish project plans and implement technologies, digital capabilities, and ways of working that improve scientific quality and delivery speed.
Requirements
- PhD in Analytical Chemistry, Pharmaceutical Sciences, Chemical Engineering, Materials Science, or a related discipline with at least 1 year of relevant pharmaceutical industry experience, or an MS with at least 5 years of relevant experience.
- At least 1 year of experience leading a small- to mid-sized team of Analytical Scientists.
- Experience driving cross-functional initiatives through matrix teams and working within CMC development teams.
- Experience leading analytical contributions to regulatory submissions and defending analytical strategies, specifications, and control strategies.
- Experience overseeing analytical activities conducted through CROs, CMOs, and external partners.
- Must be authorized to work in the United States by any employer and hold permanent U.S. work authorization; visa sponsorship is not available.
Nice to have
- Knowledge of formulation and process development, stability, specifications, product performance, and pharmaceutical manufacturing.
- Experience with multiple molecular modalities, including small molecules, peptides, or drug-linker intermediates.
- Experience with digital tools, modeling, simulation, automation, or integrated data approaches.
- Experience advancing scientific initiatives, external collaborations, analytical technologies, or improved ways of working.
Culture & Benefits
- Comprehensive health, prescription drug, dental, and vision coverage.
- 401(k) plan with matching contributions and an additional retirement savings contribution.
- Paid vacation, holidays, personal days, caregiver/parental leave, and medical leave.
- Opportunities to contribute to scientific leadership, talent development, and operational excellence.
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