What are the responsibilities and job description for the Sr Quality Control Manager position at Biovation Labs?
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