Quality Supervisor - Filling (Night Shift)

Simtrabps; Bloomington (IN); On-site; USD 75,000 - 105,000; Full time

Benefits offered by this job

Medical & Dental Coverage

401(k) Retirement Savings Plan with 0%

Paid Holidays

Paid Time Off

Education Assistance Program

Job summary

Simtra BioPharma Solutions is seeking a Quality Supervisor to join the QA Leadership Team. This role oversees Environmental Monitoring (EM) and QALO, ensuring finished products meet specifications and regulatory standards.

The supervisor supports manufacturing with effective quality oversight on the production floor. Responsibilities include leading QALO activities, training staff, authoring SOPs, and driving continuous improvement while maintaining audit readiness and regulatory compliance

Qualifications

• Bachelor’s degree (preferred science) with 2+ years in pharmaceutical quality or GXP.
• Associate’s degree with 3+ years in pharmaceutical quality or GXP.
• No degree with 5+ years in pharmaceutical quality or GXP.
• 2 years leadership experience.

Responsibilities

• Lead EM and QALO activities and ensure compliance.
• Hire, train, and evaluate personnel; empower staff.
• Provide rapid, quality-first decision making with cross-functional teams.
• Author and review SOPs, batch records, and docs.
• Maintain audit readiness and regulatory knowledge.
• Lead process/product improvement projects and data generation.

Skills

Leadership

Regulatory knowledge

Interpersonal skills

Communication

Problem solving

Education

Bachelor’s degree in science

Associate’s degree

No degree with 5+ years experience

Tools

Microsoft Office

D365

Blue Mountain

Veeva

Job description

Simtra BioPharma Solutions is seeking a Quality Supervisor to join the QA Leadership Team. This role oversees Environmental Monitoring (EM) and QALO, ensuring finished products meet specifications and regulatory standards.

The supervisor supports manufacturing with effective quality oversight on the production floor. Responsibilities include leading QALO activities, training staff, authoring SOPs, and driving continuous improvement while maintaining audit readiness and regulatory compliance