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.
