2nd Shift Finishing Supervisor – Pharmaceutical Manufacturing

Simtra BioPharma Solutions; Bloomington (IN); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Medical & Dental Coverage

401(k) Retirement Savings Plan with 6%

Paid Holidays

Paid Time Off

Education Assistance Program

Job summary

Simtra BioPharma Solutions in Bloomington, IN is seeking a Manufacturing Supervisor for the Finishing department on 2nd shift. You will lead a team on daily operations, ensure safety, quality, and adherence to cGMP while driving production schedule.

The role emphasizes hands-on leadership, strong communication, and Lean improvement initiatives. You will mentor staff, manage staffing, and partner with cross-functional teams to optimize equipment efficiency and process reliability.

Qualifications

• High School diploma or GED is required.
• Minimum 2 years of manufacturing experience is required.
• Minimum 1 year of leadership experience is required.
• Proficiency with MS Word, Excel, Outlook and enterprise software (Veeva/Trackwise/SCADA) is preferred.

Responsibilities

• Follow cGMP and safety standards in Finishing production.
• Lead and develop a team, and manage day-to-day operations.
• Supervise production scheduling, staffing, material management and audits.
• Review and approve batch documentation and see product release goals.
• Lead training programs to ensure compliant manufacturing processes.
• Drive Lean initiatives and continuous improvement on the shop floor.
• Provide guidance during deviations and conduct RCA when needed.
• Represent the company during audits and inspections.

Skills

Communication

Leadership

LEAN manufacturing

Gemba presence

Education

High School diploma or GED

Tools

Microsoft Word

Microsoft Excel

Outlook

Veeva

Trackwise

SCADA

Job description

Simtra BioPharma Solutions in Bloomington, IN is seeking a Manufacturing Supervisor for the Finishing department on 2nd shift. You will lead a team on daily operations, ensure safety, quality, and adherence to cGMP while driving production schedule.

The role emphasizes hands-on leadership, strong communication, and Lean improvement initiatives. You will mentor staff, manage staffing, and partner with cross-functional teams to optimize equipment efficiency and process reliability.