Quality Control Technician I
This position plays a key role in ensuring raw materials, in-process materials, and finished products meet established specifications and internal quality requirements. Essential Functions
Quality Control Testing & Laboratory Support
- Perform routine quality control testing on raw materials, in-process samples, and finished products according to approved methods and specifications.
- Conduct laboratory tasks including but not limited to moisture analysis, sample preparation, bulk density, pH testing, Brix testing, organoleptic evaluations, fill volume checks, weight checks, and standard preparation .
- Maintain appropriate sample handling, labeling, traceability, and retention practices.
- Ensure all testing is performed accurately, consistently, and within required timelines to support production and product release.
- Complete all laboratory documentation in compliance with Good Documentation Practices (GDP) and company standards.
- Record data clearly and accurately in laboratory notebooks, worksheets, QC forms, and electronic systems as required.
- Verify that test records are complete, traceable, and audit-ready.
- Assist with compilation and review readiness of testing data for internal and external review.
- Support review of incoming material specifications and confirm testing aligns with defined requirements.
- Assist in the review of batch records and QC documentation to support material and product disposition decisions.
- Support the release process for raw materials, packaging components, labels, in-process materials, and finished products as assigned.
- Review and organize third-party laboratory results and certificates of analysis to ensure alignment with internal specifications.
- Participate in investigations involving out-of-specification (OOS) results, deviations, nonconformances, CAPAs, and related quality events.
- Perform additional testing or re-testing as required and support documentation of findings.
- Communicate quality concerns promptly to QC leadership and assist with corrective follow-up actions.
- Perform routine equipment checks, verification activities, and calibration checks as required.
- Maintain equipment logs and report any instrument performance concerns immediately.
- Ensure laboratory equipment is maintained in a compliant and operational condition.
- Perform environmental monitoring activities as assigned, including documentation and proper filing of results.
- Support a clean, organized, and inspection-ready laboratory environment.
- Wash labware, dispose of lab waste properly, and follow safety and sanitation requirements.
- Follow all company policies and safety requirements including OSHA guidelines and PPE standards.
- Maintain compliance with dietary supplement manufacturing quality expectations and internal quality systems.
- Support ongoing quality system initiatives, continuous improvement efforts, and SOP compliance.
- Communicate testing status, delays, and quality concerns to appropriate stakeholders.
- Coordinate with production, warehouse, and quality teams to ensure efficient workflow and timely product release.
- Demonstrate a strong team-first approach that supports PRL’s culture and performance expectations.
- Perform other duties as assigned by management to support department needs and business priorities.
- Bachelor’s degree in Chemistry, Biology, Food Science, or a related discipline preferred; equivalent experience may be considered.
- 1–3 years of experience in a laboratory or manufacturing environment preferred.
- Experience in dietary supplement, pharmaceutical, food, or other regulated industries strongly preferred.
- Familiarity with GMP environments and laboratory testing practices preferred.
- Experience with laboratory instrumentation and analytical techniques is a plus.
- Strong attention to detail and ability to generate accurate, reproducible results
- Strong organizational skills and ability to manage multiple priorities effectively
- Ability to follow written procedures, specifications, and test methods
- Ability to maintain data integrity and complete documentation correctly and consistently
- Strong communication skills and ability to work cross-functionally
- Proficiency with Microsoft Office (Excel, Word) and comfort with electronic documentation systems
- Ability to work independently while maintaining a collaborative team mindset
- Work is performed in both laboratory and manufacturing environments onsite.
- Must be able to sit or stand for extended periods of time.
- Must be able to lift and carry up to 30 pounds as needed.
- May be exposed to moving machinery, noise, chemicals, powders, and temperature variations.
- Must be able to wear required personal protective equipment (PPE).
- Standard schedule is Monday–Friday; shift times may vary based on operational needs.
- Overtime may be required during peak workload periods.
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