Tedor Pharma - Cumberland, RI
posted about 1 month ago
Full-time - Mid Level
Cumberland, RI
Chemical Manufacturing
About the position
The Production Supervisor will oversee daily manufacturing operations at Tedor Pharma's facility, ensuring compliance with industry standards while leading a team of Manufacturing Associates. This role focuses on optimizing processes, supporting new product implementations, and driving continuous improvement in pharmaceutical production.
Responsibilities
- Supervise daily manufacturing operations of the facility producing pharmaceuticals.
- Provide first-line supervision to Manufacturing Associates on various shifts.
- Ensure compliance with site SOPs, EHS standards, and legal requirements.
- Support the implementation of new products and processes, including equipment changeovers.
- Develop work assignments for Manufacturing Associates to meet production schedules efficiently.
- Review GMP documents such as SOPs and BPRs.
- Accountable for the development and performance management of Manufacturing Associates.
- Lead cross-functional collaboration to achieve high-quality results.
- Optimize manufacturing processes and stand in for the Production Manager when necessary.
Requirements
- Bachelor's degree or Associate's degree with 5+ years of directly related experience.
- 3-5 years of experience in the pharmaceutical industry.
- 3 years of manufacturing supervisory experience or similar leadership role.
- Knowledge of Solid Oral Dosage/Tablet Manufacturing.
Nice-to-haves
- Strong quality/compliance orientation and track record.
- Excellent interpersonal and leadership skills.
- Strong influence and relationship-building skills with an emphasis on teamwork.
- Ability to lift 50 lbs. frequently and occasionally.
Benefits
- 401(k)
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
