Aseptic Operations Supervisor | Lead, Improve & Ensure GMP

Simtrabps; Bloomington (IN); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Medical & Dental Coverage

401(k) Retirement Savings Plan with 1:

Job summary

Simtra BioPharma Solutions in Bloomington, IN is seeking a Supervisor, Aseptic Operations to lead a team manufacturing sterile injectable products. This role reports to the Manager, Aseptic Operations and ensures compliance with cGMP, batch records, and Quality expectations.

You will collaborate with Quality, Technical Services and Engineering, develop staff, review documentation, drive continuous improvement, and support audits. Strong leadership and manufacturing experience are essential.

Qualifications

• Bachelor's Degree in science, engineering, or business preferred.
• High School diploma or GED required.
• Minimum 2 years manufacturing or operations support experience.
• Minimum 1 year leadership experience.
• Proficiency in Word, Excel, and Outlook; ability to use enterprise software.

Responsibilities

• Lead teams to execute production activities per cGMP.
• Provide guidance and leadership through daily operations.
• Interview, hire, mentor, and review staff; set objectives.
• Oversee day-to-day production, scheduling, staffing, material management, compliance, training and auditing.
• Review, approve, and manage batch and system records; assist product release.
• Develop training programs to enable compliant manufacturing.
• Lead technical reviews and process improvement projects.
• Support audits and inspections; apply RCA tools during deviations.

Skills

Leadership

Team leadership

GMP compliance

Communication

Problem solving

MS Office

ERP software

Education

Bachelor's Degree in science/engineering/business

High School diploma

Tools

Microsoft Dynamics

Veeva

PowerBI

TrackWise

Job description

Simtra BioPharma Solutions in Bloomington, IN is seeking a Supervisor, Aseptic Operations to lead a team manufacturing sterile injectable products. This role reports to the Manager, Aseptic Operations and ensures compliance with cGMP, batch records, and Quality expectations.

You will collaborate with Quality, Technical Services and Engineering, develop staff, review documentation, drive continuous improvement, and support audits. Strong leadership and manufacturing experience are essential.