Biotech Manufacturing Supervisor — Lead & Develop Teams

Lonza Group Ltd.

Portsmouth (NH)

Vor Ort

USD 85.000 - 115.000

Vollzeit

Vor 4 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Medical insurance
Dental insurance
Vision insurance
Career growth opportunities

Zusammenfassung

Lonza Group Ltd. in Portsmouth, NH is seeking a Manufacturing Supervisor to lead a team responsible for producing therapeutic proteins in a highly regulated cGMP environment.

You will drive safe, compliant, on-time manufacturing operations and partner with MSAT, Scheduling, and Engineering to meet production goals. This role emphasizes people development, process optimization, and continuous improvement, including coaching operators, reviewing batch records, and supporting recruitment and

Qualifikationen

  • Manufacturing in a cGMP-regulated environment.
  • Strong communication, problem-solving, and decision-making abilities.
  • Experience leading and developing manufacturing teams.
  • Familiarity with quality systems and GMP compliance.

Aufgaben

  • Lead daily manufacturing operations to ensure safe, compliant, and on-time execution of the production schedule.
  • Coach, train, and develop operators through performance management and career planning.
  • Monitor manufacturing activities for cGMP compliance, quality systems, SOPs, and safety standards.
  • Review batch records, logbooks, and production documentation to support timely batch release with minimal errors.
  • Coordinate cross-functional activities to troubleshoot equipment and process-related issues.
  • Support recruiting, onboarding, staffing, and workforce planning activities.

Kenntnisse

Communication
Problem-solving
Decision-making
Organizational skills

Ausbildung

Associate's or Bachelor's degree in a science-related discipline

Jobbeschreibung

Lonza Group Ltd. in Portsmouth, NH is seeking a Manufacturing Supervisor to lead a team responsible for producing therapeutic proteins in a highly regulated cGMP environment.

You will drive safe, compliant, on-time manufacturing operations and partner with MSAT, Scheduling, and Engineering to meet production goals. This role emphasizes people development, process optimization, and continuous improvement, including coaching operators, reviewing batch records, and supporting recruitment and

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