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Quality Control Chemist Jobs in Utah (NOW HIRING)

Description: QC - Chemist first shift: (9 a.m. - 5:30 p.m. M-F - start/end times somewhat flexible) 5 Months (possible extension) Salt Lake City, UT Responsibilities include: * Responsible for ...

Chemist I

Salt Lake City, UT · On-site

$30 - $33/hr

Description: 2 QC - Chemist Salt Lake City, UT First shift: (9 a.m. - 5:30 p.m. M-F 4-5 Months with possible extension Responsibilities include: * Responsible for maintaining safety and compliance ...

Provide chemistry expertise and perform miscellaneous analyses as needed; * Assist with the review and approval of product and process specifications, related to QC; * Develop and support QC wet ...

QC Lab Technician

Salt Lake City, UT · On-site

$19 - $24.25/hr

Provide chemistry expertise and perform miscellaneous analyses as needed; * Assist with the review and approval of product and process specifications, related to QC; * Develop and support QC wet ...

Quality Control

Grantsville, UT · On-site

$25 - $28/hr

Hold QC certification (preferred) * Demonstrate understanding of quality control principles and inspection methods * Have proficiency in maintaining and implementing ESD controls * Exhibit strong ...

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Quality Control Chemist information

See Utah salary details

$16

$28

$41

How much do quality control chemist jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for quality control chemist in Utah is $28.76, according to ZipRecruiter salary data. Most workers in this role earn between $23.41 and $33.27 per hour, depending on experience, location, and employer.

What is a quality control chemist?

A quality control chemist (QC chemist) is a specific type of laboratory chemist, whose primary duties are to measure and test lab materials and products according to industry-specific standard procedures. Jobs are typically in the pharmaceutical or manufacturing fields. As a QC chemist, you assure adherence to all federal regulations and safety procedures. In addition to performing rigorous quality assurance of samples, some QC chemists are responsible for calibrating and performing maintenance on lab equipment. Relevant qualifications for this career include a bachelor’s degree in chemistry, experience in a chemistry lab setting, and skills like attention to detail and the ability to multitask.

What are the key skills and qualifications needed to thrive as a quality control chemist?

To thrive as a Quality Control Chemist, you need a solid background in chemistry, analytical techniques, and a relevant bachelor's degree in chemistry or a related field. Familiarity with laboratory instruments like HPLC, GC, and spectrophotometers, as well as knowledge of regulatory standards such as GMP or ISO, is typically required. Attention to detail, problem-solving ability, and strong organizational skills are crucial soft skills for this role. These competencies ensure the accuracy, reliability, and compliance of product testing, which are vital for product safety and quality assurance.

What are some common challenges faced by quality control chemists in maintaining consistent testing standards across different production batches?

Quality Control Chemists often encounter challenges in ensuring consistency due to variations in raw materials, equipment calibration, and environmental conditions. Addressing these issues requires diligent documentation, regular equipment maintenance, and strict adherence to standard operating procedures. Effective communication with production and R&D teams is also essential to quickly resolve discrepancies and implement corrective actions, ensuring that all products meet quality and regulatory standards.

What is the difference between Quality Control Chemist vs Quality Assurance Technician?

AspectQuality Control ChemistQuality Assurance Technician
CredentialsBachelor's in Chemistry or related field; certifications like CQE beneficialBachelor's in Chemistry, Quality Management, or related; certifications like CQTA helpful
Work EnvironmentLaboratory setting, testing raw materials, in-process, and finished productsManufacturing or production environment, focusing on process compliance and documentation
Employer & IndustryPharmaceutical, food, cosmetics, chemical industriesManufacturing, pharmaceutical, food, and beverage industries

While both roles ensure product quality, the Quality Control Chemist primarily conducts laboratory testing and analysis, whereas the Quality Assurance Technician focuses on process monitoring and compliance to prevent defects. Both positions are essential for maintaining product standards in manufacturing industries.

What are popular job titles related to Quality Control Chemist jobs in Utah?

For Quality Control Chemist jobs in Utah, the most frequently searched job titles are:

What job categories do people searching Quality Control Chemist jobs in Utah look for?

The top searched job categories for Quality Control Chemist jobs in Utah are:

What are popular job titles related to Quality Control Chemist jobs in UT?

For Quality Control Chemist jobs in UT, the most frequently searched job titles are:

Infographic showing various Quality Control Chemist job openings in Utah as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, 4% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $59,823 per year, or $28.8 per hour.

Senior Manager, QC Chemistry

Denali Therapeutics

Salt Lake City, UT • On-site

Full-time

Medical, Retirement

Re-posted 10 days ago


Job description

Neurodegenerative diseases are one of the largest medical challenges of our time. Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine. Denali is founded on the collaboration of leading scientists, industry experts, and investors who share the vision that scientific discovery energetically applied to translational medicine is the key to delivering effective therapies to patients.
We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients.
The Senior Manager, QC Chemistry will serve as both a technical and people leader within the QC Chemistry group, overseeing up to 5 chemists responsible for analytical testing of biologics and related materials. This individual will ensure the delivery of safe, compliant, and on-time analytical results at scale. This is a hands-on leadership role with routine lab work (approximately 40-60%, workload-dependent) required to support critical testing, troubleshooting, and method lifecycle activities.
The ideal candidate will play a key role in supporting both clinical and commercial readiness by ensuring phase-appropriate method performance, data integrity, and operational excellence across all testing activities, with a strong emphasis on chromatography-based methods.
Key Accountabilities/Core Job Responsibilities:
  • Lead and develop QC Chemistry team; set priorities, build schedules, run tier huddles, and ensure coverage/cross-training
  • Hands-on (~50%) lab leader supporting chromatography testing, troubleshooting, record approvals, and bench mentoring
  • Own analytical method lifecycle (readiness, validation/verification/transfer); author/review protocols, reports, and change control
  • Serve as QC SME for HPLC/UPLC and core analytical techniques (e.g., UV/Vis); support biologics assays (e.g., CE-SDS, icIEF, potency) as needed
  • Ensure GMP/ALCOA+ data integrity & GDP; review/approve ELN/LIMS entries; maintain audit readiness and responses
  • Lead OOT/OOS/deviation investigations, root cause, and CAPAs; verify effectiveness and drive timely closure
  • Act as QC lead for method transfers, coordinating with AD/CMC/Manufacturing; define readiness and execute in QC
  • Oversee instrument lifecycle (URS inputs, IOQ/PQ, calibration/PM, training, release-to-use) with ENG/vendors
  • Drive operations & KPIs (TAT, investigation cycle time, schedule adherence); standardize SOPs/templates and oversee routine QC testing, stability, and sample management
  • Lead direct report(s) through goal setting, development planning, training compliance, and ongoing performance feedback

Qualifications/Skills:
  • Typically requires a BS in Chemistry, Biochemistry, or related field and 8+ years of GMP QC experience (pharma/biotech), including 3+ years of people management experience
  • Strong hands-on chromatography experience (HPLC/UPLC required)
  • Prior experience leading or mentoring small teams
  • Experience with analytical method validation, transfer, and troubleshooting
  • Strong knowledge of GMP, data integrity (ALCOA+), and QC documentation practices
  • Experience with OOS/OOT investigations, root cause analysis, and CAPAs
  • Familiarity with CDS/ELN/LIMS systems (e.g., Empower, OpenLab)
  • Biologics analytical experience (e.g., CE-SDS, icIEF, potency) is a plus, not required
  • Ability to work onsite in Salt Lake City, UT with occasional off-shift support

Compensation for the role will depend on a number of factors, including a candidate's qualifications, skills, competencies, and experience. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. Learn more at https://www.denalitherapeutics.com/careers
This compensation and benefits information is based on Denali's good faith estimate as of the date of publication and may be modified in the future.
Denali is committed to its core company value of unity by creating a diverse and inclusive environment. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class.
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