Quality Assurance Technician

somafina; Layton (UT); On-site; USD 42,000 - 60,000; Full time

Job summary

Somafina, a growing vitamins and supplements manufacturer in Layton, Utah, seeks a detail‑oriented QA/Compliance Associate to support cGMP processes and product specifications.

You will verify specifications, clear production equipment, authorize rework when needed, manage in‑process documentation, and review labels for accuracy.

Strong written and verbal communication, basic MS Office skills, and the ability to thrive under pressure in a fast‑paced environment are essential.

Qualifications

• Familiarity with GMPs; nutraceutical industry experience is a plus
• Strong written and verbal communication skills
• Comfortable following instructions while also using sound judgment within company guidelines
• Thrives under pressure in a fast-paced environment
• Sharp attention to detail and strong organizational, multitasking, and time-management skills
• Adaptable — you roll with change and stay effective when priorities shift
• A reliable, self-directed team member with high integrity
• Knowledge of Dietary Supplement GMPs and experience in the dietary supplement industry preferred
• Auditing experience a plus, but not required
• Experience enforcing SOPs and product specifications
• Proficient in MS Office, with required Excel skills
• Solid math skills and English proficiency required

Responsibilities

• Verify product specifications and ensure company policies and procedures are followed
• Clear production equipment, rooms, and packaging lines between runs
• Authorize rework when needed and perform cleaning verifications
• Review in-process documentation and manage documentation control
• Conduct yield investigations, product sampling, and point-step process reviews
• Review materials and verify labels against work orders for accuracy
• Partner with Production and Customer Service to keep projects on track and compliant with federal regulations
• Champion cGMP compliance across the facility
• Take on other tasks as assigned by your supervisor

Skills

GMP knowledge

Nutraceutical exp

Communication skills

Attention to detail

Time management

Adaptability

Integrity

MS Office (Excel)

Dietary supplement knowledge

Auditing experience

Education

High school diploma or GED

Tools

MS Office

Job description

About Somafina

Somafina is a growing, thriving third‑party manufacturer of vitamins and supplements. We're passionate about producing high‑quality products that meet the highest standards in the nutraceutical industry — and that starts with a team that cares as much about quality as we do. If you're detail‑oriented, take pride in doing things right, and want to be part of a company built on innovation and customer satisfaction, we'd love to meet you.

What You'll Do

• Verify product specifications and ensure company policies and procedures are followed
• Clear production equipment, rooms, and packaging lines between runs
• Authorize rework when needed and perform cleaning verifications
• Review in‑process documentation and manage documentation control
• Conduct yield investigations, product sampling, and point‑step process reviews
• Review materials and verify labels against work orders for accuracy
• Partner with Production and Customer Service to keep projects on track and compliant with federal regulations
• Champion cGMP compliance across the facility
• Take on other tasks as assigned by your supervisor

What You Bring

Education

High school diploma or GED, plus 1–3 months of related experience/training — or an equivalent combination of education and experience

Skills & Experience

• Familiarity with GMPs; nutraceutical industry experience is a plus
• Strong written and verbal communication skills
• Comfortable following instructions while also using sound judgment within company guidelines
• Thrives under pressure in a fast‑paced environment
• Sharp attention to detail and strong organizational, multitasking, and time‑management skills
• Adaptable — you roll with change and stay effective when priorities shift
• A reliable, self‑directed team member with high integrity
• Knowledge of Dietary Supplement GMPs and experience in the dietary supplement industry preferred
• Auditing experience a plus, but not required
• Experience enforcing SOPs and product specifications
• Proficient in MS Office, with required Excel skills
• Solid math skills and English proficiency required

Physical Requirements

This role is active and hands‑on. You'll regularly stand, walk, sit, and use your hands; occasionally lift/move up to 20 lbs. and frequently up to 10 lbs.; and need close, distant, color, and peripheral vision along with depth perception. The role may involve exposure to a dusty environment and moderate noise levels.