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Sr Quality Control Manager

Biovation Labs
Valley, UT Full Time
POSTED ON 4/16/2026
AVAILABLE BEFORE 6/15/2026

Job Summary
We are seeking an experienced and detail-oriented Sr. Quality Control Manager to lead and oversee our quality assurance and control processes within a manufacturing environment. The ideal candidate will ensure compliance with industry standards, regulatory requirements, and internal quality systems. This leadership role requires a strong understanding of quality management principles, regulatory frameworks, and project management to drive continuous improvement and maintain the highest standards of product quality. The Sr. Quality Control Manager will play a critical role in maintaining the integrity of our products and ensuring customer satisfaction.

Job Duties & Responsibilities:

Leadership & Oversight

· Lead, mentor, and develop Quality Control staff to ensure consistent execution of sampling, inspection, and testing procedures.

· Serve as the on-site quality decision-maker for in-process production issues and material release recommendations.

· Build a strong, proactive quality culture that emphasizes accountability, continuous learning, and ownership.

· Represent the Quality Control Department at leadership meetings and communicate QC trends and findings.

Operational Quality Control

· Oversee raw material, in-process, and finished-product testing programs in compliance with approved specifications and test methods.

· Manage the translation of third-party laboratory results, in-house testing, and any supplemental information into a Biovation Certificate of Analysis (COA) for product approval/release.

· Verify environmental monitoring, calibration, and maintenance of QC instruments.

· Partner with Production to ensure corrective actions for line or blend deviations are implemented effectively.

· Oversee re-qualification of expired raw materials according to GMPs.

Compliance & Coordination

· Ensure all QC activities are performed in accordance with cGMP, FDA, and company SOP requirements.

· Responsible for launching and investigating non-conformances and associated CAPAs; oversee and support OOS investigations.

· Collaborate with QA on deviation investigations, complaint assessments, and CAPA follow-up.

· Support internal and external audits, providing QC documentation and responses as needed.

· Participate in mock recalls, rework evaluations, and material review processes.

· Assist in maintaining and updating QC-related SOPs and specifications.

Continuous Improvement & Metrics

· Identify opportunities to streamline QC processes and testing efficiency.

· Track and report on key QC metrics (e.g., in-process defects, OOS rate, turnaround time) to leadership.

· Support cross-functional training and operational improvements that enhance first-pass yield and reduce waste.

· Participate in continuous improvement plans, including processes and guidelines to assist in streamlining regulatory systems and operations.

Qualifications:

· Bachelor’s degree in a scientific discipline (Chemistry, Biology, Food Science, or related field).

· Minimum 5–7 years of experience in Quality Control, preferably within dietary supplement, food, or pharmaceutical manufacturing.

· Deep understanding of cGMP and regulatory standards under 21 CFR 111 and 117.

· Demonstrated experience leading QC teams in a manufacturing environment.

· Strong analytical and decision-making skills with a hands-on approach.

· Familiarity with ERP and electronic quality systems preferred.

· Regulatory and Certification Audit Experience (NSF, SQF, FDA, Customer) strongly preferred.

· Effective communication skills both verbally and in writing.

Pay: $80,000.00 - $100,000.00 per year

Benefits:

  • 401(k)
  • 401(k) matching
  • Dental insurance
  • Employee assistance program
  • Employee discount
  • Health insurance
  • Health savings account
  • Life insurance
  • Paid time off
  • Referral program

Work Location: In person

Salary : $80,000 - $100,000

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