Production Supervisor (Temporary)

Bayer

Orizaba

Presencial

MXN 55.000 - 75.000

Jornada completa

Hace 4 días
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Descripción de la vacante

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.

Formación

  • 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.

Responsabilidades

  • 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.

Conocimientos

Supervisory experience
Aseptic processes knowledge
GMP knowledge
English communication
Microsoft Office

Educación

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

Herramientas

SAP

Descripción del empleo

Tasks And Responsibilities
  • Manage the operational activities of the area during the applicable shift through the management of assigned human and material resources.
  • Organize, control, and supervise the production processes to ensure they are carried out according to established procedures, following applicable quality, safety, environmental impact, and occupational hygiene standards.
  • Plan the deployment of current staff (vacation planning; assignment of on-site employees).
  • Monitor the integrity of manual and computerized documentation, ensuring compliance with data integrity principles.
  • Ensure that operational instructions are up to date, including the relevant training for operational staff, as well as the implementation and control of organizational security measures.
  • Coordinate the preparation and reception of audits and inspections in your area of responsibility.
  • Carry out the determination of the causes of deviations and follow up on the necessary measures, in the optimization of process engineering of production facilities, as well as in safety considerations and GMP concepts, including their testing.
  • Evaluate the production processes and their documentation, seeking optimization; as well as ensure the coordination of all activities necessary to meet the established production schedule. Follow all eBR instructions contemporaneously. Ensure the review and closure of eBRs for the batches.
  • Comply with the established standards of quality, health, safety, environmental impact, and occupational hygiene in force on site.
  • Be a role model for the principles of the Product Supply System (PSS) in your area of responsibility, leading by example and conducting yourself with the concepts and tools related to the team/colleagues (listening model, performance dialogues, GEMBAs, etc.), ensuring that activities follow the PSS methodology.
Who You Are
  • Education: Degree in Pharmaceutical Chemistry and Biology, Industrial Pharmaceutical Chemistry, Industrial Pharmacy, Chemical Engineering, Environmental Chemical Engineering, Industrial Engineering, or a related field.
  • Experience: Minimum 1 year in supervising aseptic processes.
  • Intermediate English level is desired.
  • Knowledge: Management of human and material resources, occupational hygiene, knowledge of the SAP system, aseptic processes, pharmaceutical technology, process validation.
  • Good Manufacturing Practices, Health, Safety, Environmental Impact, and Hygiene.
  • Team player, ability to work under pressure, good communication skills, Microsoft Office.

At Bayer we believe in diversity, equity and inclusion. We aim to create an environment in which everybody can feel authentic, respected and equally valued. Every day we strive to reflect our values through our unique capabilities, self-experiences, and aspirations. We intentionally seek diversity, to enable our people to bring their fullest potential out and encourage others to likewise do so. Our company wins when we leverage our capabilities to lead the cultural transformation in our business, positively impacting society.

Candidates who meet the requirements based on the job profile will be considered for employment regardless of physical disability, race, color, religion, sex, age, sexual orientation, gender identity and will not be at a disadvantage if unemployed.

Application Period: 10/14/2026 - 10/28/2026

Reference Code: 892568

Division: Pharmaceuticals Location: Mexico : Veracruz : Orizaba

Functional Area: Production&Manufacturing Work Time: Full time

Employment Type: Temporary Work

Contact Us
Address

Orizaba, México

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