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Job Description
Simtra BioPharma Solutions is seeking a Manufacturing Supervisor for its Finishing department in Bloomington, Indiana. This role is crucial for supporting daily operations, ensuring the safe and efficient execution of the production schedule, and maintaining compliance with cGMP and safety standards. The Supervisor will lead a team, optimize equipment efficiency, and identify continuous improvement opportunities using LEAN Manufacturing principles.
Responsibilities:
- Provide guidance and leadership to the production team.
- Supervise day-to-day production, scheduling, and staffing.
- Review and manage documentation for batch and system records.
- Implement training programs and internal auditing programs.
- Lead technical reviews, investigations, and process improvement projects.
- Resolve technical and cGMP problems.
- Author Non-conformance investigation reports (NCRs).
Requirements:
- High School diploma or GED required.
- Minimum 2 years of manufacturing experience required.
- Minimum 1 year leadership experience required.
- In-depth process knowledge of related manufacturing equipment and processes preferred.
- Experienced understanding of cGMPs and other regulatory guidelines applicable to the medical/pharmaceutical industry preferred.
- Computer proficiency in Microsoft Word, Excel, and Outlook.
Simtra BioPharma Solutions offers:
- Day One Benefits, including Medical & Dental Coverage.
- Flexible Spending Accounts.
- Life and AD&D Insurance.
- Short and Long-Term Disability Insurance.
- 401(k) Retirement Savings Plan with Company Match.
- Paid Time Off and Paid Holidays.
- Adoption Reimbursement Program.
- Education Assistance Program.
- Employee Assistance Program.
- Onsite Campus Amenities, including a Workout Facility and Cafeteria.
