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Production Supervisor-1st Shift
5 months ago
- Location: Saint Paul, Minnesota
- Type: Direct Hire
- Job #67065
- Salary: $72,800
Leading pharmaceutical company is looking for a Production Supervisor to join their team in Saint Paul, MN. This is a direct hire position
Shift of the Production Supervisor:
Monday - Friday 6:00am - 2:30pm
Responsibilities of the Production Supervisor:
- Safety leader on the floor who ensures that all safety policies, procedures, and requirements are adhered to by the production staff, visiting customers, and management staff. Expected to track and lead the safety audit program to build a culture of safety.
- Provide day-to-day leadership and "on the floor" management for each team to ensure the necessary materials, equipment, and documentation are available so the manufacturing tasks can be executed as efficiently as possible.
- Active participant in Quality programs within . Embodies 's commitment to producing the highest quality products through adherence and diligence to current Good Manufacturing Practices.
- Provide appropriate transitional shift information to ensure smooth operation throughout shift changes. Will also communicate policies and procedures to production staff, as necessary.
- Production floor leader accountable for understanding the needs and abilities of the team.
- Training and coaching of production staff through Standard Operating Procedures (SOPs), cGMPs, technical experience, and continuous improvement. Ensures production personnel are current with required training curriculum.
- Writes and conducts annual performance reviews to direct reports. Upholds 's Key Behaviors of Teamwork, Customer Service, Entrepreneurship, Accountability and Leadership.
- Collects all relevant production data in a master data file for review and analysis of shift performance and other Key Performance Indicators (KPI's). Reviews and assesses the yield rates for potential areas of improvement.
- Reviews production floor documentation for proper entries to release the production line for operation. Upon completion of product runs, reviews all entries in the Master Batch Record.
- Collaborate with functional support departments such as: Scheduling, Engineering, Quality, Materials Management, Project Management and Purchasing.
- All other tasks as assigned.
- High School degree or equivalent, required. Associate or Bachelor's Degree in science related discipline, preferred.
- 5+ years of experience in cGMP manufacturing environment, preferably in pharmaceutical or medical device industries.
- 2+ years of supervisory/leadership experience strongly preferred.
DAVIS Companies partners with the top employers locally and nationally. They choose us because of our reputation for finding high quality talent, fast, but also our experience for evaluating and representing the best candidates in the marketplace. We make every effort to provide updates and feedback to candidates at each stage of the process as we appreciate how stressful looking for a new role can be. Apply today and experience "The DAVIS Difference".
