Quality Assurance Technician

Pharmatech, Inc.; Lindon (UT); On-site; USD 42,000 - 58,000; Full time

Job summary

Pharmatech Labs in Lindon, Utah, is seeking a bilingual Quality Assurance Technician (English & Spanish) to ensure quality and safety of all products. You will perform sampling, testing, and inspection of raw materials, in-process products, and finished goods per CFR Part 111 & 117, working with powders, liquids, and packaging materials.

The role requires a high school diploma (associate/bachelor’s preferred) with GMP knowledge, strong attention to detail, and effective teamwork.

Qualifications

• High school diploma or equivalent; associate or bachelor’s degree in a related field preferred.
• Previous experience in quality or similar role in the dietary supplement or food industry.
• Knowledge of CFR Part 111 & 117 (GMPs).
• Strong attention to detail and organized skills.
• English and Spanish language proficiency.

Responsibilities

• Inspect and sample raw materials for transfer to QC Lab.
• Perform in-process testing to ensure product meets specs.
• Complete monitoring records and ensure documentation accuracy.
• Conduct final inspections of pallets and labeling accuracy.
• Assist with labeling verification and MMR/BPR review.

Skills

Bilingual English/Spanish

Attention to detail

Communication and teamwork

Quality assurance mindset

Education

High school diploma or equivalent

Associate or Bachelor’s degree in a related field preferred

Tools

Scales with significant figures

pH meters

Density meters

QC monitoring instruments

Job description

Job Title:Quality Assurance Technician

Location:Lindon, Utah

Company:Pharmatech Labs

About Us:

Pharmatech Labs, located in Lindon, Utah, is a premier nutritional contract manufacturer specializing in liquid and powder supplements. We offer comprehensive, accelerated, one-stop-shop services, including; Concept development, Research and development, Customization and flavor work, In-house laboratory testing, Quality manufacturing, and Packaging and kitting.

Our mission is to enhance lives by being the most customer-focused manufacturer of health products, delivering an unparalleled experience in the development and production of nutritional products.

Job Type:Full Time

Shifts Needed: Swing Shift

Schedule:

Days: M-Th: 4:30pm - 3:00am, with occasional Fridays required during high volume periods.

JOB SUMMARY

We are looking for a Bilingual Quality Assurance Technician(English & Spanish). The Quality Assurance Technician performs a critical role to ensure the quality and safety of all products we manufacture. You will be responsible for performing routine sampling, testing, and inspection of raw materials, in-process products, and finished goods in accordance with CFR Part 111 & 117. This includes working with powders, liquids, and packaging materials.

DUTIES & RESPONSIBILITIES

Incoming Materials:

• Collect, prepare, inspect, sample, process and document all raw materials to be transferred to QC Lab (retention of packaging materials as well).
• Ensure samples are transferred to QC Lab in a timely manner.
• Ensure controlled and efficient storage of retain samples to allow for safe storage and easy retrieval.
• Ensure completeness of verifications and accuracy throughout all documentation.
• Perform cleaning procedures in the sampling booths to ensure no cross-contact of allergens or cross- contamination of bacteria.
• Create and place expiration date stickers on all raw materials.
• Ensure that all raw materials have allergens declared and enforce Allergen Management Program.

In-Process / Manufacturing:

• Perform in-process testing throughout the production process (at set frequencies) to ensure product meets specification and quality standards. (this differs based on product, and customer requirements)
• Fill out monitoring records for in-process testing, and AQLs with Good Documentation Practices to meet federal regulations such as CFR 111 & 117 as well as customer expectations.
• Perform Double Label Verification checks for production.

Finished Product Release:

• Final inspection of every completed pallet to ensure labels reflect the correct information, label placement, overall quality and case count.
• Inspection of trailers prior to loading them with finished pallets to ensure there is no foreign materials that would jeopardize the quality and safety of all products.
• Final review and scanning of MMR/BPR records for release.
• Releasing SKU/Lot in JDE Software.

QUALIFICATIONS

• High school diploma or equivalent; associate or bachelor’s degree in a related field preferred.
• Previous experience in quality or similar role in the dietary supplement or food industry.
• Knowledge of CFR Part 111 & 117 (GMPs).
• Strong attention to detail and organized skills.
• Must be able to speak, read, write, and understand English.
• Must be able to speak and understand Spanish.
• Excellent communication and teamwork abilities.
• Proficiency in using scales (significant figures), pH meters, density meters, and other instruments for quality control monitoring.

Physical Requirements:

• Ability to lift and carry up to 50 pounds.
• Ability to stand, walk, and perform repetitive tasks for extended periods.
• Ability to work in a manufacturing environment with exposure to noise and varying temperatures.

WORKING CONDITIONS

Full-Time position on Swing Shifts; may require occasional overtime. Work is performed in a warehouse & production setting.

Benefits:

• Comprehensive health, dental, and vision insurance.
• 401(k) plan with company match.
• Paid Time Off.
• Paid Holidays.
• Professional development and training opportunities.

Pharmatech Labs is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.