On-Site Sterile GMP Manufacturing Supervisor

Alcami Corporation

Morrisville (NC)

In loco

USD 70.000 - 90.000

Tempo pieno

2 giorni fa
Candidati tra i primi

Una candidatura completa in un minuto

Curriculum e lettera di presentazione personalizzati, pronti da inviare.

Supera i filtri ATS

Descrizione del lavoro

Alcami Corporation seeks a Manufacturing Supervisor to lead GMP operations for sterile injectable products from discovery to distribution. You will oversee a 4–12 person manufacturing team, ensure SOP and batch record adherence, and drive performance in a fast‑paced, on‑site environment.

Role requires at least 2 years in a regulated cgmp setting, with preference for a Bachelor’s degree. 5% travel and 12‑hour day shifts may apply.

Competenze

  • Requires a high school diploma or GED; a bachelor's degree is preferred.
  • Minimum 2+ years of hands-on CGMP experience.
  • Experience with CGMP Drug Product manufacturing required.

Mansioni

  • Follow SOPs and CGMPs to execute manufacturing protocols.
  • Ensure training compliance and timely completion of requirements.
  • Supervise manufacturing activities including cleaning, equipment prep, dispensing, and filling.
  • Communicate effectively with cross-functional teams and management.
  • Direct supervise 4–12 direct reports and drive shift performance.
  • Maintain timekeeping and manage time-off requests to keep operations running.
  • Collaborate on quality issues and implement process improvements.
  • Support batch releases, investigations, and CAPA activities.
  • Assist in hiring and onboarding for manufacturing staff.
  • Perform other duties as assigned.

Formazione

High School Diploma or GED
Bachelor’s degree

Strumenti

Light inspection booths
Autoclaves
pH meters
Filtration equipment
Isolator aseptic filling

Descrizione del lavoro

Alcami Corporation seeks a Manufacturing Supervisor to lead GMP operations for sterile injectable products from discovery to distribution. You will oversee a 4–12 person manufacturing team, ensure SOP and batch record adherence, and drive performance in a fast‑paced, on‑site environment.

Role requires at least 2 years in a regulated cgmp setting, with preference for a Bachelor’s degree. 5% travel and 12‑hour day shifts may apply.

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