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Quality Control Analyst Jobs in Utah (NOW HIRING)

QC Lab Technician

Salt Lake City, UT · On-site

$19.25 - $24.25/hr

Salt Lake City, UT The QC Lab Technician will perform routine operations of organoleptic testing, QC analytical instrumentation (including, but not limited to HPLC, UPLC, GC-MS, FTIR, ICP-MS ...

QC Lab Technician

Salt Lake City, UT · On-site

$19 - $24.25/hr

QC Lab Technician Department: QC Lab Location: Salt Lake City, UT The QC Lab Technician will ... Verify and maintain all analytical instrumentation; * Assist with development of methods; * Provide ...

Strong analytical and organizational skills with the ability to monitor performance trends ... as a QC ManagerIAT-II Baseline Certification (Security+, CYSA, et al.)Minimum ...

We are hiring a Quality Control Manager for an exciting opportunity. and Responsibilities The ... Strong analytical and organizational skills with the ability to monitor performance trends ...

We are hiring a Quality Control Manager for an exciting opportunity. and Responsibilities The ... Strong analytical and organizational skills with the ability to monitor performance trends ...

Operate PMI and Spectrometer Analyzer for metal analysis and verification. * Implement programs for ... Experience in quality control or quality assurance inspection. * Experience in the electronic ...

Operate PMI and Spectrometer Analyzer for metal analysis and verification. * Implement programs for ... Experience in quality control or quality assurance inspection. * Experience in the electronic ...

Operate PMI and Spectrometer Analyzer for metal analysis and verification. * Implement programs for ... Experience in quality control or quality assurance inspection. * Experience in the electronic ...

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Quality Control Analyst information

See Utah salary details

$15

$25

$37

How much do quality control analyst jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for quality control analyst in Utah is $25.41, according to ZipRecruiter salary data. Most workers in this role earn between $21.01 and $28.22 per hour, depending on experience, location, and employer.

What is a quality control analyst?

A quality control (QC) analyst or quality assurance analyst tests computer programs to ensure that software applications function properly before being deployed in production or going to market. As a quality control analyst, your job is to identify and fix bugs in software applications and computer systems and make recommendations to management about how to improve a software application’s functionality, user experience (UX), and user interface (UI). Your QC process typically involves a significant amount of collaboration with other analysts and software developers.

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

To thrive as a Quality Control Analyst, you need a solid understanding of quality assurance principles, data analysis, and laboratory or manufacturing processes, often supported by a degree in a related scientific or technical field. Familiarity with tools such as LIMS (Laboratory Information Management Systems), statistical software, and regulatory standards (like GMP or ISO) is typically required. Attention to detail, problem-solving abilities, and strong communication skills help analysts identify issues and collaborate effectively with team members. These skills ensure products or processes consistently meet quality standards, safeguarding consumer safety and organizational reputation.

What are some common challenges faced by quality control analysts, and how can they be effectively managed?

Quality Control Analysts often encounter challenges such as tight production deadlines, variability in sample quality, and adapting to frequent changes in testing protocols or regulatory standards. Managing these challenges involves strong organizational skills, proactive communication with production and laboratory teams, and staying current with industry regulations. Developing efficient documentation practices and using digital tools for data management can also help maintain accuracy and streamline workflow, ultimately supporting consistent product quality.

What is the difference between Quality Control Analyst vs Quality Assurance Specialist?

AspectQuality Control AnalystQuality Assurance Specialist
CertificationsOften requires certifications like ASQ CQE or ISO auditorSimilar certifications, with focus on process audits
Work EnvironmentLaboratory, manufacturing, or production settingsOffice-based, process review, and compliance environments
Primary FocusTesting products, identifying defects, ensuring quality standardsDeveloping and maintaining quality systems, preventing defects
Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, software, healthcare industries

While both roles aim to ensure product quality, the Quality Control Analyst primarily tests and inspects products to identify defects, whereas the Quality Assurance Specialist focuses on creating and improving processes to prevent defects. Both roles often require similar certifications and work in related environments, but their core responsibilities differ in focus and approach.

How much does a quality control analyst earn?

The average salary for a quality control analyst typically ranges from $45,000 to $70,000 per year, depending on experience, industry, and location. Entry-level positions may start lower, while experienced analysts with certifications can earn higher salaries. Many roles also include benefits such as health insurance and paid time off.

What are the most commonly searched types of Quality Control Analyst jobs in Utah?

The most popular types of Quality Control Analyst jobs in Utah are:

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

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

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

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

Infographic showing various Quality Control Analyst job openings in Utah as of August 2026, with employment types broken down into 87% Full Time, and 13% Contract. Highlights an 100% In-person job distribution, with an average salary of $52,861 per year, or $25.4 per hour.

Quality Control Analyst I

Teva Pharmaceuticals

Salt Lake City, UT • On-site

$23.25 - $31.25/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.


Teva Pharmaceuticals USA rating

8.6

Company rating: 8.6 out of 10

Based on 26 frontline employees who took The Breakroom Quiz

16th of 86 rated pharmaceutical


Job description

We Are Teva
We're Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it's innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we're dedicated to addressing patients' needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.
Our Team, Your Impact
This position is responsible for performing testing and analysis of incoming materials, intermediates, finished products, swab samples, and other samples to support the commercial and development activities at the site in compliance with all regulatory requirements, company policies and procedures.
How You'll Spend Your Day
All areas of responsibility listed below are essential to the satisfactory performance of this position by any incumbents with reasonable accommodation if necessary. Any non-essential functions are assumed to be included in other related duties or assignments.
  • Responsible for testing and analyzing incoming materials such as intermediates, finished products and swab samples.
  • Responsible for preparing, maintaining and reviewing thorough records, documentation on solutions, sample preparation and investigational/experimental samples.
  • Responsible for supporting laboratory investigations into Out of Specification/Out of Trend results or other laboratory events.
  • Responsible for performing revisions to documentation such as Standard Operating Procedures, Test Methods and Specifications.
  • Responsible for coordinating and sending materials for contract laboratory testing.
  • Responsible for compliance with DEA and site requirements regarding the handling, use and disposal of controlled substances.
  • Responsible for performing verification of compendial methods.
  • Responsible for providing training to other analysts on activities for which they have developed a level of expertise.
  • Responsible for performing peer review on documents which may also become a full-time role.
  • Responsible for assisting with activities associated with the stability program including sampling and statistical analyses.
  • Responsible for assisting with activities related to the sampling of incoming materials as needed.
  • Responsible for maintaining work areas and performing job functions in a safe and efficient manner in accordance with company policies and procedures, Good Manufacturing Practices (cGMP's), Standard Operating Procedures (SOP's) and Batch Record instructions.
  • Responsible for performing additional related duties as assigned.

Your Skills and Experience
Any equivalent combination of education, training and/or experience that fulfills the requirements of the position will be considered.
Education/Certification/Experience:
  • Requires a Bachelor's degree, preferably in Chemistry or Microbiology, or equivalent education/experience with a minimum of 3 years relevant progressive experience in a Quality Control Laboratory environment.
  • Solid understanding of the principles of analytical chemistry as it applies to HPLC, GC, FTIR, UV-Vis and other general analytical techniques.
  • Requires working knowledge of cGMP, DEA and other applicable industry regulatory requirements as they relate to the production of pharmaceutical products and associated quality systems.
  • Prefer experience with Laboratory Information Management Systems (Labware LIMS and/or Empower preferred).

Also Good to Have
Skills/Knowledge/Abilities:
  • Computer proficiency with comprehensive working knowledge of MS Office products, Learning Management Systems (LMS), ERP systems such as SAP or Oracle and manufacturing/quality systems such as LIMS, Trackwise and Qdocs.
  • Ability to effectively document a process, explaining scientific and/or technical ideas in writing (technical writing skills).
  • Ability to communicate effectively with excellent written and oral communication skills.
  • Ability to interact positively and collaborate with co-workers, management and other internal stakeholders.
  • Self-directed with ability to organize and prioritize work.
  • Detail oriented with ability to identify errors and/or inconsistencies while performing tasks.

Problem Solving:
  • Works on problems of moderate scope where evaluation of contributing factors requires analysis of situation or data.
  • Exercises judgment within broadly defined practices and policies and selects methods and techniques for obtaining solutions.
  • Selects methods, techniques, and evaluation criteria for obtaining results.
  • Acts independently and proactively to recommend methods and procedures for problem resolution.

WORKING ENVIRONMENT
  • Exposure to fumes, odors, dusts, mists or gasses (for non-office).
  • Exposure to moving mechanical parts or moving equipment.
  • Exposure to low to moderate to loud noise levels.
  • May be required to wear personal protective equipment (PPE) as needed for assigned area and/or process (i.e. safety glasses, gloves, hearing protection, etc.).

How We'll Take Care of You
At Teva, better health starts from within, and that includes you. From day one, you'll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community. When it comes to your career, you'll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you'll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way.
We offer a competitive benefits package, including:
• Comprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment, providing the employee enrolls.
• Retirement Savings: 401(k) with employer match, up to 6% and an annual 3.75% Defined Contribution to the 401k plan.
• Time Off: Paid Time Off including vacation, sick/safe time, caretaker time and holidays.
• Life and Disability Protection: Company paid Life and Disability insurance.
• Additional benefits include, but are not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible , Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more.
Already Working @Teva?
Make sure to apply through our internal career site on Twist-your one-stop shop for career development
Teva's Equal Employment Opportunity Commitment
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.
Please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Request a reasonable accommodation by sending an email to disabilityassistance@tevapharm.com with the nature of your request and your contact information. Only inquiries concerning a request for a reasonable accommodation will be responded to from this email address.
Important notice to Employment Agencies - Please Read Carefully
Teva Pharmaceuticals USA does not accept unsolicited assistance from agencies for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

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