Manufacturing Head, Millburn Site (Millburn) Job at Novartis, Millburn, NJ

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  • Novartis
  • Millburn, NJ

Job Description

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Summary

At Advanced Accelerator Applications, a Novartis company, we are committed to leading innovation in nuclear medicine and delivering the next generation of targeted radioligand therapy to cancer patients. We are looking for an experienced pharmaceutical leader to help us reach our ambitious goals.

The Manufacturing Head is responsible for leading a manufacturing facility in achieving all objectives in key areas such as Safety, Supply, Cost, Quality, and People for a GMP Radioligand Therapies Production Site. The leader is responsible for translating Novartis Manufacturing and Supply and Country strategies into actionable plans including preparation and execution of capital projects; continuously improving operational efficiencies at the site; ensuring the site has adequate resources and capabilities to ensure CGMP compliance, quality, service to patients, and people development.

About The Role

Key responsibilities:

  1. Direct and manage Production, HSE (Safety), Engineering, Supply Chain and Manufacturing Science & Technology activities.
  2. Lead the site leadership team comprising department heads from each function, monitoring performance to company goals through established metrics, and driving cross-site collaboration.
  3. Ensure compliance with cGMP, safety rules, and other applicable regulations across the site, people, operations, and processes.
  4. Coordinate site activities through planning to meet manufacturing objectives in a timely and cost-effective manner.
  5. Collaborate with other Site Heads to establish processes and procedures, standardize where possible, and adapt as needed for site-specific needs.
  6. Partner with functional leadership to establish production and quality standards and develop controls.
  7. Develop and communicate the site strategic plan aligned with company objectives.
  8. Provide leadership, mentorship, and development opportunities to site employees, fostering a positive work environment.
  9. Lead site meetings to ensure compliance with policies, safety regulations, and procedures, and facilitate discussions on company initiatives.
  10. Promote a culture of respect, support, and personal investment among employees.

Essential Requirements

  1. BSc in chemical engineering, chemistry, pharmacy, or a related field, or equivalent experience.
  2. At least 10 years in the pharmaceutical industry, with 5+ years in leadership roles, including sterile manufacturing.
  3. Strategic thinking and enterprise focus.
  4. Strong collaboration skills, experience in matrix organizations.
  5. Ability to analyze data and summarize outcomes effectively.
  6. Deep knowledge of cGMPs.
  7. Ability to prioritize and work under pressure.
  8. Effective communication skills and ability to inspire large teams.

Desirable Requirements

  • Training in radiochemistry or radiopharmaceuticals.

Benefits and Rewards: Refer to our handbook for details: .

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Job Tags

Full time,

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