Overview
Quality Engineer Jobs in Lindon, UT at Pharmatech Labs
Title: Quality Engineer
Company: Pharmatech Labs
Location: Lindon, UT
Company Description
Pharmatech Labs is a nutritional contract manufacturer of liquid and powder supplements located in Lindon, UT. We offer research & development services, fulfillment, warehousing, in-house lab work/testing, and quality control. Our high-tech production facility is capable of producing liquids, capsules, blisters, powders, stick packs, gusseted bags, pouches, jars, and tubs.
Role Description
This is a full-time on-site role for a Quality Engineer at Pharmatech Labs in Lindon, UT. Quality Engineer (QE) performs a key function in maintaining and improving the Quality Management System (QMS) at Pharmatech. QE is a leadership and customer-facing role requiring clear understanding and execution of quality and regulatory requirements. When performed well, the QE naturally bolsters the company reputation and customer relationships, providing an unrivaled experience through communication, transparency, collaboration, and improvement.
Responsibilities Include, but are not limited to:
· Act as a liaison between Pharmatech and the client addressing quality issues and resolutions.
· Lead root cause analysis efforts in response to customer complaints and/or non-conformities (NCRs).
· Ensure that communications with customers are thorough, yet clear and concise.
· Play an active role in identifying opportunities to improve quality processes and systems.
· Conduct internal audits to ensure compliance with regulatory requirements, company policies, and standard operating procedures.
· Participate in external (regulatory, certification, and customer) audits.
· Work closely with the manufacturing team to ensure quality standards are understood and consistently applied.
· Provide training and support to manufacturing staff on quality standards and best practices.
· Participate and present in regular Material Review Board (MRB) meetings.
· Track and trend the health of the QMS, and present in annual Management Review meeting.
Qualifications
Strong analytical and problem-solving skills
Attention to detail and quality-focused mindset
Knowledge of FDA regulations and GMP standards
Bachelor’s degree in a technical discipline
3+ years experience in quality or related function in FDA regulated industry
