2 часа назад
Associate Director, Process & Analytical Development (Pharmaceutical Manufacturing)
155 700 - 181 650$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Associate Director, Process & Analytical Development (Pharmaceutical Manufacturing): Leading process and analytical development, project-specific manufacturing activities, and organizational readiness for future pharmaceutical manufacturing operations with an accent on GMP compliance, technology transfer, validation, and scale-up. Focus on building high-performing teams, planning capacity and resources, driving Lean and digital transformation, and coordinating complex facility startup and expansion initiatives.
Location: Initially remote in the United States; transition to an on-site U.S. East Coast or Midwest location is anticipated as the project progresses, expected in 2027. Monday–Friday, 8:00 a.m.–5:00 p.m.
Salary: $155,700–$181,650 gross annual base salary, plus performance-related bonus.
Company
operates more than 30 sites across five continents and supports the development and manufacturing of medicines and life-science products.
What you will do
- Lead, coach, and develop the Process & Analytical Development team while building accountability, collaboration, safety, and continuous improvement.
- Set strategic direction through long-range planning, portfolio prioritization, resource allocation, budgeting, and performance management.
- Ensure process development, analytical development, and project-specific manufacturing activities are delivered safely, compliantly, on time, in full, and within budget.
- Support Sales & Operations Planning by aligning capabilities, capacity, and organizational structures with customer demand.
- Lead facility startup, operational readiness, validation, manufacturing scale-up, technology transfer, and process development initiatives.
- Drive Lean maturity, digital tools, automation, data-driven decision-making, governance, risk management, and succession planning.
Requirements
- Master’s degree in engineering, life sciences, pharmaceutical sciences, chemistry, biochemistry, or a related scientific discipline.
- At least 10 years of progressive leadership experience in pharmaceutical, biotechnology, process development, analytical development, or manufacturing operations.
- Deep understanding of small-molecule and bioconjugate technologies, small-molecule drug-substance manufacturing, GMP environments, and pharmaceutical commercialization.
- Experience with facility startups, technology transfers, validation programs, operational readiness, greenfield or brownfield expansions, and large-scale capital projects.
- Ability to lead cross-functional work with Engineering, Quality, Manufacturing, MSAT, Automation, EH&S, Finance, and Human Resources.
- Knowledge of Lean Manufacturing, Six Sigma, digital systems, automation technologies, and data integrity principles, with strong executive communication and problem-solving skills.
Culture & Benefits
- Performance-related bonus.
- Medical, dental, and vision insurance.
- 401(k) matching plan.
- Life insurance and short- and long-term disability insurance.
- Employee assistance programs and paid time off.
- Culture centered on collaboration, accountability, excellence, passion, integrity, safety, and innovation.
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