Pharmaceutical Production Supervisor
Not Disclosed•Full-TimeOn-site
location_onOn-site
About the Role
We are seeking a hands-on and experienced Production Supervisor (2nd Shift) to oversee daily operations in a highly regulated manufacturing environment. This role is critical for executing production schedules efficiently while ensuring full compliance with cGMP, SOPs, and safety standards. The ideal candidate will possess strong leadership abilities, a deep understanding of consumer products or pharmaceutical manufacturing, and a proven track record in supervising teams on the shop floor.
In this position, you will lead and manage operators and support staff during the 2nd shift (Monday through Friday, 3:00 PM - 11:30 PM). Your day will involve conducting regular audits, ensuring accurate documentation, and guiding the execution of change control processes. You will also collaborate closely with process engineers, maintenance personnel, and management to maintain equipment readiness and resolve mechanical issues promptly. A key part of your mission is to foster a clean, safe working environment and to train, coach, and assess team members to drive continuous improvement.
About ttg Talent Solutions
At ttg, "We believe in making a difference One Person at a Time." As a recruiting agency, we are committed to creating an inclusive and diverse work environment. We welcome applications from all qualified candidates regardless of race, color, religion, gender, sexual orientation, national origin, age, disability, or veteran status.
Application & Hiring Process
Please note that all offers of employment are contingent upon the successful completion of a drug test and background check. We maintain a drug- and substance-free workplace to ensure the safety and well-being of all employees.
Work location
Work model: On-site
On-site
Key Responsibilities
- check_circleExecute and oversee production activities per the approved daily schedule
- check_circleLead and manage operators and support staff during the 2nd shift
- check_circleConduct regular audits and spot-checks to ensure compliance with GMP and SOPs
- check_circleEnsure all documentation is completed accurately and timely
- check_circleDirect and support the facility cleaning team to maintain a safe environment
- check_circleGuide execution of change control processes and corrective actions
- check_circleTrain, coach, and assess team members while managing performance reviews
- check_circleCollaborate with maintenance personnel to ensure equipment readiness
- check_circleMaintain shift continuity through thorough documentation and handoff communication
Requirements
- verifiedHigh School Diploma or equivalent
- verifiedMinimum of 2 years of experience as a Production Lead or Supervisor in a manufacturing environment
- verifiedSupervisory experience in a regulated industry
- verifiedStrong knowledge of cGMP, SOPs, production scheduling, and quality/compliance systems
Nice to Have
Previous work in consumer product or active pharmaceutical ingredient (API) production. Familiarity with deviation investigations, technology transfers, and change control systems. Experience leading shift operations in a union or non-union manufacturing environment.
