Quality Control (QC) Technician

Life Solutions – Vista, CA (On-Site)

$21–$23/hour | Full-Time | Hourly

Life Solutions is an FDA-registered, GMP-certified OTC dietary supplement manufacturer located in Vista, CA. As our team grows, we are seeking a detail-oriented Quality Control (QC) Technician to support laboratory testing and product release activities in a GMP environment. The QC technician plays a crucial role in delivering products that meet the highest standards of quality.

Position Summary

The QC Technician performs sampling, testing, documentation, and release support for raw materials, in-process materials, packaging components, labels, and finished products in accordance with approved specifications and SOPs. In this role, you will be responsible for ensuring that all products meet strict quality standards and comply with industry regulations. Your will help maintain the integrity of our products, uphold safety standards, and support continuous improvement initiatives. This position offers an exciting opportunity to contribute to high-quality manufacturing processes in a growing environment dedicated to excellence.

Key Responsibilities

• Perform testing of raw materials, in-process blends, packaging components, labels, and finished products.
• Conduct thorough quality inspections using precision testing instruments.
• Perform purity and potency testing of new and existing raw materials, inspect incoming ingredients, evaluate samples, and qualify materials to ensure they meet approved specifications prior to release.
• Conduct visual inspection of raw materials, in-process materials, packaging components, labels, and finished products to verify identity, integrity, labeling accuracy, and overall compliance with specifications.
• Coordinate third-party testing on products and equipment certifications.
• Execute pass/fail determinations per approved specifications.
• Maintain accurate laboratory documentation and QC logs.
• Review Certificates of Analysis (CoAs) and supporting records.
• Apply release labels and coordinate with QA for final approval.
• Support deviation investigations and maintain compliance with GMP requirements.
• Maintain laboratory equipment logs and testing records.
• Follow and adhere to approved Standard Operating Procedures (SOPs) for sampling, testing, documentation, and material/product release activities in compliance with GMP requirements.
• Review and assist in drafting, revising, and maintaining Quality Control SOPs, test methods, and specification documents in accordance with GMP requirements and document control procedures.
• Operate and calibrate advanced testing tools to ensure accuracy in quality assessments.
• Collect and analyze data related to product quality, documenting findings in detail for review and reporting purposes.
• Support the production team by identifying root causes of defects and collaborating on corrective actions aligned with FDA regulations and GMP standards.
• Assist in implementing and maintaining quality systems that promote continuous improvement and uphold industry best practices.
• Perform routine quality audits in accordance with OTC manufacturing standards to verify compliance with quality management systems.
• Participate in internal and external quality audits and inspections, providing detailed reports and ensuring corrective measures are effectively executed.

Qualifications

• 1–3 years of QC experience in a manufacturing environment required.
• Hands-on testing and documentation required.
• Associate’s or Bachelor’s degree in Chemistry, Biology, or related science preferred.
• Pharmaceutical, OTC/dietary supplement, or GMP facility experience preferred.
• Working knowledge of industry standards including FDA cGMP requirements, specifically 21 CFR Part 211 (Dietary Supplements), and NSF/ANSI 455-2 standards preferred.
• Experience with batch record review preferred.
• Ability to interpret results accurately.
• Strong documentation skills and attention to detail.
• Self-driven and motivated.
• High standards for quality and excellence.
• Clear and effective communicator of technical information.
• Team player with strong collaboration skills.
• Familiarity with analytical testing and quality management software a plus.

Work Environment

Life Solutions offers a collaborative, quality-focused working environment. This is an on-site role in Vista, CA.

Job Types: Full-time, Permanent

Pay: $21.00 - $23.00 per hour

Expected hours: 40 per week

Benefits:

• Paid time off
• Retirement plan

People with a criminal record are encouraged to apply

Work Location: In person

Salary : $21 - $23