15 часов назад
Associate Director, CDMO Alliance Management (Pharmaceutical Manufacturing)
169 222 - 253 000$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Associate Director, CDMO Alliance Management (Pharmaceutical Manufacturing): Managing the end-to-end lifecycle of contract development and manufacturing organization partnerships with an accent on strategic sourcing, contract negotiation, governance, and supplier performance. Focus on strengthening supply-chain resilience, assessing GMP and operational risks, and coordinating cross-functional responses to manufacturing incidents and disruptions.
Location: Princeton, NJ, United States
Salary: $169,222–$253,000 annually, plus incentive opportunity.
Company
is a pharmaceutical company developing and delivering healthcare products and services.
What you will do
- Act as the central business partner and point of contact for Contract Development and Manufacturing Organizations (CDMOs).
- Lead partner selection, contract negotiations, governance structures, and executive business reviews.
- Define and monitor KPIs covering CDMO delivery, quality, and operational performance.
- Assess supply-chain and partner-site risks and drive improvement measures based on performance data.
- Coordinate cross-functional responses to major incidents, regulatory changes, demand volatility, and manufacturing deviations.
- Support decisions on new CDMO selections and major capital investments, including business-side assessments during GMP audits.
Requirements
- Bachelor’s degree in Science, Engineering, Business, or a related field; an MBA or advanced degree is preferred.
- 8–12+ years of experience in alliance management, strategic sourcing, or external manufacturing in the pharmaceutical or biotech industry.
- Experience influencing and collaborating with stakeholders in complex, matrixed organizations and with international colleagues.
- Strong expertise in risk management, business continuity planning, KPI-based performance analytics, negotiation, and supplier relationship management.
- Knowledge of the CDMO landscape and manufacturing processes across modalities such as small molecules, biologics, and sterile fill-finish.
- Thorough knowledge of GMP requirements, including CFR Title 21 Parts 210–211 and Part 600, as well as EU, MHRA, and other global health authority regulations.
Culture & Benefits
- Comprehensive medical, dental, vision, and prescription drug coverage.
- Company-provided life, accidental death and dismemberment, and short- and long-term disability insurance.
- Tuition reimbursement and student loan assistance.
- Generous 401(k) match, flexible time off, paid holidays, and paid leave programs.
- Culture emphasizing accountability, strategic problem solving, patient and customer centricity, impactful communication, respectful collaboration, and professional development.
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