Pharmatech, Inc. Jobs Hiring Now
Pharmatech, Inc. is hiring for 8 open roles on Migrate Mate as of July 16, 2026, concentrated in business operations and manufacturing operations. Migrate Mate updates Pharmatech, Inc.'s live openings daily. Pharmatech, Inc. is a contract manufacturing and production company serving the dietary supplement and personal care industries, with roles spanning manufacturing, quality, and warehouse operations.
Find Pharmatech, Inc. JobsOverview
Pharmatech, Inc. hiring data on Migrate Mate, as of July 16, 2026.
- Open jobs
- 8
- Top team
- Business Operations
- Seniority
- Across all levels
- Work type
- 0% remote or hybrid
- Top location
- Lindon
Open Roles at Pharmatech, Inc.
Showing 8 of 8+ Pharmatech, Inc. jobs
At Pharmatech, we make life better! We are committed to building a positive and supportive culture of transparency and honesty, striving for the well-being of our teams, customers, and community. We offer competitive compensation, benefits, and opportunities for continuous growth. Our core values are people, customer service, team, and continuous improvement. If this aligns with your personal core values, please apply to join our team!
Industry: Dietary Supplement Co-Manufacturing
Employment Type: Full-Time, On-Site
Job Summary:
This is a full-time on-site role for a Quality / Documentation Specialist at Pharmatech Labs in Lindon, UT. This is a key role on the Quality Compliance team, responsible for maintaining and improving the Quality Management System (QMS), as well as generating reviewing, and or approving compliance documentation. This is a customer-facing role requiring strong verbal and written communication skills and understanding of regulatory requirements, thereby maintaining the company reputation and customer relationships - providing an unrivaled experience through communication, transparency, collaboration, and improvement.
Employment Type: Full-Time, On-Site
Key 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.
- Support 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.
Education & Experience:
- Bachelor’s degree in a relevant field preferred
- Experience in a quality role, in an FDA regulated industry / working in a co-manufacturing or contract manufacturing environment is highly desirable.
Required Skills & Abilities:
- Strong technical writing skills
- Excellent problem-solving and analytical skills
- Detail-oriented with a strong focus on accuracy and compliance
- Effective communication and interpersonal skills to interact with clients and internal teams
- Understanding of quality systems and cGMP / GDP standards
- Familiar with FDA, NSF/NSF Sport, SQF, ISO, 21 CFR 111, and other regulatory requirements preferred
- Ability to manage complex projects with clear priorities in a fast-paced environment
Working Conditions:
- Office and manufacturing environment
- Standard working hours with flexibility to address urgent client needs or quality issues as they arise
At Pharmatech, we make life better! We are committed to building a positive and supportive culture of transparency and honesty, striving for the well-being of our teams, customers, and community. We offer competitive compensation, benefits, and opportunities for continuous growth. Our core values are people, customer service, team, and continuous improvement. If this aligns with your personal core values, please apply to join our team!
Industry: Dietary Supplement Co-Manufacturing
Employment Type: Full-Time, On-Site
Job Summary:
This is a full-time on-site role for a Quality / Documentation Specialist at Pharmatech Labs in Lindon, UT. This is a key role on the Quality Compliance team, responsible for maintaining and improving the Quality Management System (QMS), as well as generating reviewing, and or approving compliance documentation. This is a customer-facing role requiring strong verbal and written communication skills and understanding of regulatory requirements, thereby maintaining the company reputation and customer relationships - providing an unrivaled experience through communication, transparency, collaboration, and improvement.
Employment Type: Full-Time, On-Site
Key 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.
- Support 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.
Education & Experience:
- Bachelor’s degree in a relevant field preferred
- Experience in a quality role, in an FDA regulated industry / working in a co-manufacturing or contract manufacturing environment is highly desirable.
Required Skills & Abilities:
- Strong technical writing skills
- Excellent problem-solving and analytical skills
- Detail-oriented with a strong focus on accuracy and compliance
- Effective communication and interpersonal skills to interact with clients and internal teams
- Understanding of quality systems and cGMP / GDP standards
- Familiar with FDA, NSF/NSF Sport, SQF, ISO, 21 CFR 111, and other regulatory requirements preferred
- Ability to manage complex projects with clear priorities in a fast-paced environment
Working Conditions:
- Office and manufacturing environment
- Standard working hours with flexibility to address urgent client needs or quality issues as they arise
Job Roles at Pharmatech, Inc.
Working at Pharmatech, Inc.
Pharmatech, Inc.'s 8 open roles are across all levels, and about 0% are remote or hybrid. The most active teams are business operations and manufacturing operations. Pharmatech, Inc. operates in the contract manufacturing and production space, supporting dietary supplement and personal care product lines through blending, compounding, packaging, and quality functions. Roles typically require hands-on work in regulated production environments. Most Pharmatech, Inc. roles are based in Lindon.
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Browse jobs by rolePharmatech, Inc. Jobs: Frequently Asked Questions
How many jobs is Pharmatech, Inc. hiring for right now?
Pharmatech, Inc. is hiring for 8 open roles on Migrate Mate as of July 16, 2026, updated daily, concentrated in business operations and manufacturing operations. Roles span manufacturing, warehouse, and quality functions at its production facilities. Migrate Mate pulls the latest openings directly so the count reflects what Pharmatech, Inc. is actively recruiting for.
What kinds of roles does Pharmatech, Inc. hire for?
The most active teams are business operations and manufacturing operations. Pharmatech, Inc. regularly hires for production and manufacturing positions including blending operators, compounding and fill operators, packaging associates, sanitation technicians, and raw material handlers, as well as quality and document specialists and warehouse material handlers. Most postings are across all levels, with an emphasis on hands-on production floor work.
Are Pharmatech, Inc. jobs remote or in-person?
Mostly on-site. About 0% of Pharmatech, Inc.'s open roles on Migrate Mate are remote or hybrid as of July 16, 2026, with the rest based in Lindon. Each Pharmatech, Inc. listing shows its work location so you can filter before applying.
How do I apply to a job at Pharmatech, Inc.?
Find a Pharmatech, Inc. role that fits on Migrate Mate, then follow the listing through to Pharmatech, Inc.'s own application page to submit your materials directly. Pharmatech, Inc. manages its own hiring process, including screening and interviews. Migrate Mate keeps the listings current so you're applying to roles Pharmatech, Inc. is actively filling.
Does Pharmatech, Inc. hire entry-level?
Most of Pharmatech, Inc.'s open roles on Migrate Mate are across all levels as of July 16, 2026. Check individual Pharmatech, Inc. listings for stated experience requirements.
Where is Pharmatech, Inc. hiring?
Most Pharmatech, Inc. roles are based in Lindon, and about 0% offer remote or hybrid work as of July 16, 2026. Migrate Mate shows the location on each listing.