Production Supervisor (Temporary)

Bayer AG; Orizaba; On-site; MXN 420,000 - 680,000; Full time

Job summary

Bayer AG in Mexico seeks a Production Supervisor with a background in pharmaceutical manufacturing and aseptic processes. The role focuses on supervising shifts, managing staff and materials, and maintaining GMP, health, and safety standards.

Strong documentation, planning, and SAP usage are required to ensure quality and on-time production. Applicants should have at least one year in aseptic supervision, good communication skills, and the ability to work under pressure in a highly regulated

Qualifications

• Education in Pharmaceutical Chemistry, Biology, or related field as listed.
• Minimum 1 year supervising aseptic processes.
• Knowledge of GMP, health, safety, and environmental standards.
• Experience with SAP and good numerical documentation skills.

Responsibilities

• Oversee area operations during shifts with staff and materials.
• Organize production processes following procedures and quality standards.
• Plan deployment of current staff including vacations.
• Ensure documentation integrity and up-to-date operational instructions.
• Coordinate audits and inspections within area of responsibility.
• Investigate deviations and optimize production and safety measures.
• Review processes and ensure alignment with production schedule.

Skills

Aseptic processes

Teamwork

Communication

Microsoft Office

Intermediate English

SAP

Education

Bachelor's degree in Pharmaceutical Chemistry or Industrial Pharmacy or related field

Tools

SAP

Job description

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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.