Production Supervisor (3rd Shift 10p-6:30a)
Teva Pharmaceuticals
June 25, 2026
On-site
Davie, FL
Operations
3rd Shift M-F 10p-6:30a
Responsibilities:
- Direct and oversee manufacturing operations under general supervision; ensure safe execution and compliance with cGMP and SOPs.
- Supervise and coordinate manufacturing schedule to meet production requirements; assign/delegate work to hourly personnel.
- Ensure training compliance (100%); provide ongoing cGMP and safety training.
- Assure operations comply with batch records, SOPs, and cGMP; revise batch records and SOPs as required.
- Coordinate with Quality Control for intermediate and final product release.
- Review/approve time sheets; support hiring, training, problem resolution, delegation, attendance tracking, disciplinary actions, and performance evaluations.
- Maintain equipment and safety rule compliance; maintain management presence on the manufacturing floor and apprise Manufacturing Manager of issues.
- Improve efficiency by analyzing/correcting equipment/processing problems; troubleshoot with minor adjustments.
- Coordinate with materials management and quality assurance documentation; interface with vendors for new equipment.
Qualifications:
- Bachelor’s degree or equivalent plus 7+ years responsible supervisory experience in the pharmaceutical industry (preferably manufacturing).
Skills/Abilities:
- Resource management; basic computer/word processing; English communication; clear oral/written communication.
- Selecting/training/supervising/evaluating staff; handle multiple tasks; resolve inquiries/complaints.
- Analyze and troubleshoot moderate–complex problems; recommend and administer solutions independently.
Benefits (including):
- Comprehensive health insurance; 401(k) with match and defined contribution; paid time off; life and disability insurance; additional listed benefits.
Application:
- Apply through the internal career site on Twist.
Responsibilities:
- Direct and oversee manufacturing operations under general supervision; ensure safe execution and compliance with cGMP and SOPs.
- Supervise and coordinate manufacturing schedule to meet production requirements; assign/delegate work to hourly personnel.
- Ensure training compliance (100%); provide ongoing cGMP and safety training.
- Assure operations comply with batch records, SOPs, and cGMP; revise batch records and SOPs as required.
- Coordinate with Quality Control for intermediate and final product release.
- Review/approve time sheets; support hiring, training, problem resolution, delegation, attendance tracking, disciplinary actions, and performance evaluations.
- Maintain equipment and safety rule compliance; maintain management presence on the manufacturing floor and apprise Manufacturing Manager of issues.
- Improve efficiency by analyzing/correcting equipment/processing problems; troubleshoot with minor adjustments.
- Coordinate with materials management and quality assurance documentation; interface with vendors for new equipment.
Qualifications:
- Bachelor’s degree or equivalent plus 7+ years responsible supervisory experience in the pharmaceutical industry (preferably manufacturing).
Skills/Abilities:
- Resource management; basic computer/word processing; English communication; clear oral/written communication.
- Selecting/training/supervising/evaluating staff; handle multiple tasks; resolve inquiries/complaints.
- Analyze and troubleshoot moderate–complex problems; recommend and administer solutions independently.
Benefits (including):
- Comprehensive health insurance; 401(k) with match and defined contribution; paid time off; life and disability insurance; additional listed benefits.
Application:
- Apply through the internal career site on Twist.