Aseptic Production Supervisor

Bayer; Orizaba; On-site; MXN 55,000 - 75,000; Full time

Job summary

Bayer in Orizaba, Veracruz is seeking a Production Supervisor to lead area operations, manage resources, and ensure compliant production under safety standards.

You will coordinate staff deployments, review documentation, and support audits while fostering a culture of quality and continuous improvement.

This temporary, full-time role requires a degree in pharmaceutical or engineering fields and at least 1 year supervising aseptic processes.

Qualifications

• Minimum 1 year supervising aseptic processes.
• Intermediate English is desired.
• Knowledge of GMP, SAP, and process validation.
• Experience managing human and material resources in a production environment.

Responsibilities

• Manage operational activities of the area during the shift with available staff and materials.
• Organize and supervise production processes to meet quality, safety, and environmental standards.
• Plan staff deployment and vacation coverage.
• Ensure documentation integrity and adherence to data standards.
• Keep operational instructions up to date and train staff accordingly.
• Coordinate audits and inspections in your area.
• Investigate causes of deviations and implement corrective actions.
• Ensure production schedules are met and eBR closures completed.
• Uphold product supply system principles in daily work.
• Lead by example and promote safety and hygiene.

Skills

Supervisory experience

Aseptic processes knowledge

GMP knowledge

English communication

Microsoft Office

Education

Degree in Pharmaceutical Chemistry and Biology, Industrial Pharmaceutical Chemistry, Industrial Pharmacy, Chemical Engineering, Environmental Chemical Engineering, Industrial Engineering, or related field

Tools

SAP

Job description

Bayer in Orizaba, Veracruz is seeking a Production Supervisor to lead area operations, manage resources, and ensure compliant production under safety standards.

You will coordinate staff deployments, review documentation, and support audits while fostering a culture of quality and continuous improvement.

This temporary, full-time role requires a degree in pharmaceutical or engineering fields and at least 1 year supervising aseptic processes.