About The Position

Join a collaborative team where you’ll help manufacture life‑changing therapies. You’ll guide operations in a cGMP environment and contribute directly to delivering high‑quality products to patients and efficient production activities throughout the night schedule. Shift Schedule: Shift: Rotational Night Shift (7:00 PM – 7:00 AM) Pattern: 2 on, 2 off, 3 on, 2 off, 2 on, 3 off (repeating cycle) Starting off: First 2-week orientation and training period is on the day shift Additional Pay: Nights and weekend shifts include additional pay

Requirements

  • AS/BS degree in a science field; HS diploma with relevant experience may be considered.
  • 5–10 years of experience in a GMP or manufacturing environment.
  • Strong communication skills and the ability to coach and support team members.
  • Proven critical‑thinking and problem‑solving abilities for daily manufacturing challenges.
  • Ability to follow procedures, maintain accurate records, and uphold quality standards.
  • Ability to work in cleanrooms and lift up to 50 lbs.

Nice To Haves

  • 1–4 years of supervisory or team‑leading experience preferred.
  • Experience working in cleanroom environments and with automated or manual systems preferred.

Responsibilities

  • Lead safe, compliant daily operations in a manufacturing suite.
  • Plan schedules and assign tasks to meet production goals.
  • Review batch records and logbooks for clarity and accuracy.
  • Coach and develop operators through ongoing feedback and training.
  • Partner with cross‑functional teams to resolve obstacles.
  • Troubleshoot equipment and process issues as they arise.
  • Support deviations, SOP updates, and continuous improvement efforts.

Benefits

  • An agile career and dynamic working culture.
  • An inclusive and ethical workplace.
  • Compensation programs that recognize high performance.
  • Medical, dental and vision insurance.
  • Our full list of global benefits can be found here: https://www.lonza.com/careers/benefits.
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