Aseptic QA Supervisor – Evening Shift (Onsite)

Kindeva

Brentwood (MO)

Ibrido

USD 85.000 - 115.000

Tempo pieno

3 giorni fa
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Curriculum e lettera di presentazione personalizzati, pronti da inviare.

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Descrizione del lavoro

Kindeva is hiring a QA Supervisor – Aseptic to lead QA activities in the Sterile Product Manufacturing (SPM) building onsite. The role emphasizes supervision of inspectors, maintaining staffing, and ensuring inspections and batch records meet GMP/GDP standards.

The ideal candidate has aseptic processing knowledge, experience with regulatory requirements, and the ability to partner with Production and QA Management to resolve issues and drive continuous improvement.

Competenze

  • Bachelor's or associate's degree in a technical or science-related discipline, with relevant experience and/or training.
  • Minimum of two years of aseptic manufacturing experience.
  • Supervisory experience in pharmaceutical or medical device manufacturing is preferred.

Mansioni

  • Supervise, plan, and coordinate daily activities of Quality Assurance colleagues during the shift.
  • Coordinate shift staffing, training, vacations, and absences to ensure QA coverage.
  • Ensure training and qualification curricula are maintained for direct reports.
  • Generate daily shift reports for Quality and Production Management.
  • Attend daily shift huddles and Gemba meetings.
  • Review batch records for conformance to procedures and GMP/GDP requirements.
  • Maintain gowning qualifications and support aseptic processing areas.

Conoscenze

Aseptic processing principles
GMP/GDP compliance
Leadership/Supervisory
Team collaboration
Quality systems

Formazione

Bachelor's or Associate's degree in science/technical field

Strumenti

TrackWise
SAP
PRISM

Descrizione del lavoro

Kindeva is hiring a QA Supervisor – Aseptic to lead QA activities in the Sterile Product Manufacturing (SPM) building onsite. The role emphasizes supervision of inspectors, maintaining staffing, and ensuring inspections and batch records meet GMP/GDP standards.

The ideal candidate has aseptic processing knowledge, experience with regulatory requirements, and the ability to partner with Production and QA Management to resolve issues and drive continuous improvement.

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