Aseptic Process Engineer II | Contamination Control Coach

Worklane GmbH

Greenville (SC)

Sur place

USD 85 000 - 120 000

Plein temps

14 jours+

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Résumé du poste

Bausch + Lomb in Greenville, SC is seeking an Aseptic Process Engineer and Aseptic Core Coach to strengthen sterility assurance in sterile solutions manufacturing. You will coach shop-floor personnel, assess aseptic practices, and support training, qualification, and continuous improvement across manufacturing areas and shifts.

The role collaborates with Quality, Engineering, Regulatory Affairs, and site leadership to reduce contamination risk, ensure GMP readiness, and sustain compliance with

Qualifications

  • Bachelor’s degree in microbiology, biology, chemistry, or engineering.
  • Minimum 4 years in aseptic manufacturing or related cGMP environment.
  • Knowledge of aseptic processing, cleanroom behavior, and environmental monitoring.
  • Experience training or coaching in a controlled manufacturing environment.
  • Strong analytical, writing, and communication skills.

Responsabilités

  • Observe gowning, disinfection, material transfer, and aseptic connections.
  • Provide coaching to personnel and leaders to reinforce compliant practices.
  • Support aseptic training curricula and qualification activities.
  • Document observations and deviations following data integrity requirements.
  • Participate in investigations and CAPA development.

Connaissances

Aseptic processing
Cleanroom discipline
Environmental monitoring
Data analysis
Coaching / training

Formation

Bachelor’s degree in microbiology or related field

Outils

CAPA system
GxP documentation

Description du poste

Bausch + Lomb in Greenville, SC is seeking an Aseptic Process Engineer and Aseptic Core Coach to strengthen sterility assurance in sterile solutions manufacturing. You will coach shop-floor personnel, assess aseptic practices, and support training, qualification, and continuous improvement across manufacturing areas and shifts.

The role collaborates with Quality, Engineering, Regulatory Affairs, and site leadership to reduce contamination risk, ensure GMP readiness, and sustain compliance with

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