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Pharmaceutical Production Supervisor

2 months ago

Bridgeton, Missouri, United States Virbac Full time
Job Description

**Job Title:** Pharmaceutical Production Supervisor

**Company:** Virbac Animal Health

**Location:** Bridgeton, MO

**Job Type:** Full-time

**About Us:

Virbac Animal Health is a leading manufacturer of pharmaceutical products for animals. We are seeking a highly skilled Pharmaceutical Production Supervisor to join our team.

Responsibilities:
  • **Team Management:** Lead, direct, train, and provide support to shift personnel. Ensure employees understand duties, responsibilities, policies, and procedures, including product batch record instructions.
  • **Productivity:** Pre-shift preparation, organize team's activities in relation to production schedule, ensure availability of supplies and equipment according to production needs, maintain inventory of miscellaneous production supplies and parts, monitor and assess department work flow and daily task activities, monitor KPIs, enhance productivity and product quality levels, support new product introductions by participating in operational mastery and corresponding training.
  • **Regulatory Compliance/Quality:** Ensure operational and pharmaceutical mastery of units and processes, direct supervision of production in compliance with SOPs and regulating agencies' rules, review product batch records for accuracy of entries, compliance to established limits, specifications, and presence of all verification signatures, provide hands-on leadership to ensure Quality and Compliance, participate in writing and/or updating GMP documentation in coordination with QA, write and/or update local operating procedures, participate in qualification and validation in the unit.
  • **Continuous Improvement:** Propose, participate, and/or lead kaizen events, perform operating system through Gemba walk, continuously identify and lead improvements in units and processes, participate in waste reduction in order to increase effectiveness and efficiency of manufacturing operations.
  • **Troubleshooting:** Participate in detecting deviations in collaboration with team, perform thorough root cause analysis and understand other kinds of root cause analysis tools, lead deviation investigations and participate in CAPA with QA, manage deviations and exceptions in collaboration with QA, process engineer.
  • **Safety:** Ensure compliance with Safety Program, ensure employees work safely in accordance with regulations, standards, and procedures, eliminate unreasonable risk to health and the environment, report all safety and/or environmental incidents to Safety Manager.
  • **Training:** Identify and anticipate team's skill requirements and propose training programs, coordinate individual training for team in accordance to required curricula.
Requirements:
  • **Education:** BS in Chemistry/Engineering with a minimum of 5 years in the pharmaceutical industry or at least 10 years of experience in the pharmaceutical industry with part of the experience as a Supervisor.
  • **Skills:** Prior operational pharmaceutical experience, knowledge of chemical safety and advanced analytical troubleshooting, supervisory and continuous improvement experience, experience supervising in a union environment is beneficial, pass prerequisite test assessments.

**What We Offer:** Excellent benefits package, including generous time off, 401k + match, life, medical, dental, and vision benefits, and more.