Aseptic Operations Supervisor – Sterile Pharma

Simtra-Biopharma-Solutions; Bloomington (IN); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Medical & Dental Coverage

401(k) Retirement Savings Plan with 2%

Paid Holidays

Paid Time Off

Adoption Reimbursement Program

Job summary

Simtra BioPharma Solutions is seeking a Supervisor, Aseptic Operations to lead a team engaged in sterile injectable manufacturing. You will ensure compliance with cGMP, oversee batch records, and coordinate with Quality, Technical Services, and Engineering for smooth operations.

You will interview, hire, mentor, and conduct annual reviews, while maintaining strong on-floor leadership and safety practices. Bloomington, IN site with comprehensive benefits.

Qualifications

• Bachelor's degree in a science, engineering, or business discipline strongly preferred.
• High school diploma or GED required.
• Minimum 2 years of manufacturing or operations support experience.
• Minimum 1 year leadership experience.

Responsibilities

• Understand, follow, coach, and lead teams to execute production activities in accordance with cGMP.
• Provide guidance, support, direction and leadership through daily interactions.
• Interview, hire, mentor and develop staff; conduct annual performance reviews.
• Supervise day-to-day production, scheduling, staffing, material management, compliance, training and auditing to meet deadlines and quality standards.
• Review, approve, and manage documentation for batch and system records; assist in release of product for distribution.
• Develop and implement training programs to ensure compliant manufacturing processes.

Skills

Leadership

Gemba presence

Cross-functional communication

Education

Bachelor's degree in science/engineering/business

High School diploma or GED

Tools

Microsoft Word

Microsoft Excel

Microsoft Outlook

Microsoft Dynamics

Veeva

PowerBI

Trackwise

Job description

Simtra BioPharma Solutions is seeking a Supervisor, Aseptic Operations to lead a team engaged in sterile injectable manufacturing. You will ensure compliance with cGMP, oversee batch records, and coordinate with Quality, Technical Services, and Engineering for smooth operations.

You will interview, hire, mentor, and conduct annual reviews, while maintaining strong on-floor leadership and safety practices. Bloomington, IN site with comprehensive benefits.