Quality Assurance Supervisor

Federal-Package-Network; Chanhassen (MN); On-site; USD 75,000 - 105,000; Full time

Benefits offered by this job

Full benefits package

401(k) with company contributions

Paid time off & leave

Flexible scheduling

Education reimbursement program

Culture that values you

Job summary

Federal Package in Chanhassen, MN seeks a Quality Assurance Supervisor to lead QA operations and ensure compliance with cGMPs, SOPs, and regulatory standards. The role oversees audits, CAPA, deviations, and continuous improvement while guiding a QA team to achieve product quality and efficiency.

Requirements include a Bachelor’s in a science/quality field, 5+ years QA experience in manufacturing, and FDA/ISO audit exposure. Strong leadership and communication are essential.

Qualifications

• Bachelor’s degree in Science, Quality, Engineering, or related field.
• 5+ years of Quality Assurance experience, preferably in manufacturing.
• Experience leading or supervising a team, directly or indirectly.
• Experience with FDA and/or ISO audits.
• Knowledge of cGMPs, quality systems, CAPA, deviations, and root cause investigations.
• Experience with internal audits and continuous improvement.
• Strong written, verbal, and interpersonal communication skills.
• Strong attention to detail, organization, and problem-solving skills.
• Ability to confidently make independent decisions.
• Six Sigma Green Belt certification preferred but not required.

Responsibilities

• Supervise and support Quality Assurance Technicians/Inspectors.
• Oversee daily QA operations and serve as the SME and primary escalation point for QA-related issues.
• Ensure compliance with cGMPs, SOPs, specifications, and regulatory requirements.
• Review batch records and manufacturing documentation for accuracy and compliance.
• Perform quality audits of raw materials, packaging, labels, and finished products.
• Investigate deviations, complaints, and nonconforming materials and support CAPAs.
• Oversee root cause analysis and CAPA development, implementation, and effectiveness.
• Participate in internal, FDA, ISO, and customer audits.
• Support IQ, OQ, and PQ validation activities.
• Create and maintain QA SOPs, work instructions, and quality programs.
• Ensure appropriate training on GMPs, quality systems, and applicable regulatory requirements.
• Lead continuous improvement initiatives focused on product quality, compliance, efficiency, and risk reduction.
• Partner with Manufacturing, Engineering, Supply Chain, and other teams to resolve quality issues.
• Monitor quality trends and support proactive quality improvement.
• Train employees on GMPs, quality procedures, and quality expectations.

Skills

cGMPs knowledge

FDA/ISO audits

CAPA & deviations

Root cause investigations

Leadership/Supervision

Quality systems

Independent decision making

Strong communication

Education

Bachelor’s degree in Science/Quality/Engineering

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Quality Assurance Supervisor

Full Time Regular Management Chanhassen, MN, US

Salary Range: $75,000.00 To $105,000.00 Annually

Who You Are

You are a quality-focused leader with experience in a regulated manufacturing environment and a strong understanding of cGMPs, FDA requirements, and quality systems. You are detail-oriented, organized, and confident making independent decisions. You communicate effectively and have the ability to lead, coach, and develop a QA team while applying strong critical-thinking and continuous-improvement skills.

What You’ll Do

• Supervise and support Quality Assurance Technicians/Inspectors.
• Oversee daily QA operations and serve as the SME and primary escalation point for QA-related issues, providing guidance on quality, compliance, regulatory, and product-related matters.
• Ensure compliance with cGMPs, SOPs, specifications, and regulatory requirements.
• Review batch records and manufacturing documentation for accuracy and compliance.
• Perform quality audits of raw materials, packaging, labels, and finished products.
• Investigate deviations, complaints, and nonconforming materials and support CAPAs.
• Oversee root cause analysis and CAPA development, implementation, and effectiveness.
• Participate in internal, FDA, ISO, and customer audits.
• Support IQ, OQ, and PQ validation activities.
• Create and maintain QA SOPs, work instructions, and quality programs.
• Ensure appropriate training on GMPs, quality systems, and applicable regulatory requirements.
• Lead continuous improvement initiatives focused on product quality, compliance, efficiency, and risk reduction.
• Partner with Manufacturing, Engineering, Supply Chain, and other teams to resolve quality issues.
• Monitor quality trends and support proactive quality improvement.
• Train employees on GMPs, quality procedures, and quality expectations.

What You’ll Bring

• Bachelor’s degree in Science, Quality, Engineering, or a related field.
• 5+ years of Quality Assurance experience, preferably in manufacturing.
• Experience leading or supervising a team, either directly or indirectly.
• Experience with FDA and/or ISO audits.
• Knowledge of cGMPs, quality systems, CAPA, deviations, and root cause investigations.
• Experience with internal audits and continuous improvement.
• Strong written, verbal, and interpersonal communication skills.
• Strong attention to detail, organization, and problem-solving skills.
• Ability to confidently make independent decisions.
• Six Sigma Green Belt certification preferred but not required.

Physical Demands

• Vision Requirements: This position requires the ability to perform tasks involving close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.
• Color Differentiation: The role requires the ability to visually compare colors against established reference standards, including standard color solutions or approved reference materials. The position also requires the ability to accurately identify color-coded labels, status tags, and chemical hazard warnings within the work environment.
• Sensory Evaluation (Odor Detection): The position may require the ability to detect and differentiate odors during the evaluation of raw materials and finished products in accordance with applicable USP monographs and/or internal testing specifications. This includes identifying unexpected or out-of-specification (OOS) odors that may indicate contamination, degradation, or spoilage.
• Material/Product Appearance Evaluation: The position requires the ability to visually evaluate the appearance of raw materials and finished products as required by applicable USP monographs and internal testing specifications, including identifying irregularities or deviations from established standards.

Why Federal Package?

As we continue to grow, we’re actively investing in our people, our technology, and our future. That means this is the perfect time to join our team and make your mark. You’ll have the opportunity to contribute meaningfully, take ownership of your work, and help shape the direction of our organization. Whether you’re passionate about innovation, leadership, or operational excellence, there’s room to grow here.

At Federal Package we believe that you work your best when you feel your best. Here is what you can expect from us:

• Comprehensive Benefits Package: Medical, dental, vision, life insurance, and disability coverage.
• Retirement Support: 401(k) with company contributions to help you plan for your future.
• Generous PTO & Leave: Paid time off, volunteer time, bereavement leave, and new parent paid leave.
• Flexible Scheduling: Flex time and support for work-life balance.
• Education Reimbursement Program: We invest in your continued personal and professional development.
• A Culture That Values You: Your energy, ideas, and ambition will be recognized and rewarded.