Pharmaceutical Production Supervisor

Location: Bridgeton

** Experiencing together a unique human adventure
** Animal health is key to the health of the planet. Working at Virbac means taking part in a unique human adventure in which the engagement of each individual contributes to its evolution. Encouraging internal mobility between positions and countries, offering individual development plans and building a partnership based on trust between managers and employees are as many perspectives of motivation for our teams.

We also offer them a work environment conducive to exploring new territories and balancing their professional and personal lives. Finally, fostering their engagement to animal health also means listening to them and helping them to acquire new skills, preparing them for the challenges of tomorrow and encouraging them to contribute to an ever more responsible approach to our business.
** Virbac Animal Health is seeking a Pharmaceutical Production Supervisor for our Production Team. The Production Supervisor is a  Direct Supervisor of Union Operators and temporary employees in the mixing, granulation, formulation, compression and packaging of pharmaceutical products.
Responsible for operational mastery, safety, quality, productivity, regulatory compliance, continuous improvement, cost improvements  and employee training.
**** Responsabilities
* ***** Area of responsibility 1: [Team Management].
****** Main activities
**** Lead, direct, train and provide support to shift personnel
**** Assure employees understand duties, responsibilities, policies and procedures including product batch record instructions
**** Set and achieve objectives, both departmental and team
**** Empower and motivate team members
**** Foster dialogue and relationships
**** Participate in recruitment
****** Expected results:
** Guarantees motivation, development and performance of team and collaborators.  Maintains a good atmosphere and working conditions.
****** Area of responsibility 2: [Productivity]
****** Main activities
**** Pre shift preparation
**** Organize team’s activities in relation to production schedule
**** Ensures availability of supplies and of 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 to new product introductions by participating in operational mastery and corresponding training
****** Expected results:
** Guarantee performance of production to meet customer demand.
****** Area of responsibility 3: [Regulatory Compliance/Quality].
****** Main activities
**** Ensure the operational and pharmaceutical mastery of their units and processes
**** Direct supervision of production in compliance with our SOPs and regulating agencies’ rules.
**** Reviews 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
****** Expected results:
** Ensure employees work within regulations, standards and procedures
****** Area of responsibility 4: [Continuous Improvement]
****** Main activities
**** Propose, participate and/or lead kaizen events
**** Perform their operating system through Gemba walk
**** Continuously identify and lead improvements in their units and processes
**** Participate in waste reduction in order to increase effectiveness and efficiency of manufacturing operations
****** Expected results:
** Improve production performance, quality, safety delivery and customer service.
****** Area of responsibility 5: [Troubleshooting]
****** Main activities
**** Participate in detecting deviations in collaboration with their team
**** Perform a 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…