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Biotech Manufacturing Associate Jobs in Sandy, UT

Carterra

Quality Technician

Salt Lake City, UT · On-site

$17.50 - $23.50/hr

... leading pharmaceutical and biotechnology companies to thoroughly explore new worlds in ... The position will also support a variety of activities necessary to support Manufacturing ...

New

Amgen

Strategic Sourcing Manager

Salt Lake City, UT · On-site

$124K - $161K/yr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Reporting to the Associate Director of Strategic Sourcing, you will lead the global sourcing ...

All JobsBiotech Manufacturing Associate JobsBiotech Manufacturing Associate Jobs in Sandy, UT

Biotech Manufacturing Associate information

See Sandy, UT salary details

$11

$19

$31

How much do biotech manufacturing associate jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for biotech manufacturing associate in Sandy, UT is $19.80, according to ZipRecruiter salary data. Most workers in this role earn between $15.53 and $22.16 per hour, depending on experience, location, and employer.

What is a biotech manufacturing associate?

Biotech Manufacturing Associates are professionals who work in the production of biotechnology products, such as pharmaceuticals, vaccines, and other biologically derived materials. They are responsible for operating equipment, following strict protocols, and maintaining sterile environments to ensure product quality and safety. Their duties often include preparing materials, monitoring production processes, troubleshooting equipment issues, and documenting all activities according to regulatory standards. This role is essential in ensuring that biotech products are manufactured efficiently and meet both industry and government regulations.

What are the key skills and qualifications needed to thrive as a biotech manufacturing associate?

To thrive as a Biotech Manufacturing Associate, you typically need a background in biology, chemistry, or a related field, along with experience in GMP-regulated environments. Familiarity with bioprocessing equipment, laboratory instrumentation, and documentation systems such as batch records is crucial. Attention to detail, teamwork, and strong problem-solving abilities help you excel in this collaborative and regulated field. These skills ensure the consistent production of safe, high-quality biotech products while maintaining compliance with industry standards.

What are some common challenges faced by biotech manufacturing associates, and how can they be managed effectively?

Biotech Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP), troubleshooting equipment malfunctions, and working under tight production deadlines. Effective management of these challenges involves strong attention to detail, proactive communication with cross-functional teams such as quality assurance and engineering, and continuous learning to stay updated on new protocols and technologies. Developing problem-solving skills and embracing a collaborative mindset can also help associates consistently contribute to high-quality production outcomes.

What is the difference between Biotech Manufacturing Associate vs Laboratory Technician?

AspectBiotech Manufacturing AssociateLaboratory Technician
CredentialsHigh school diploma or equivalent; some roles may require associate degreeHigh school diploma or equivalent; some roles may require associate degree or certification
Work EnvironmentManufacturing floor, production lines, cleanroomsLaboratories, research facilities, testing environments
Industry UsageBiotech manufacturing, pharmaceutical productionResearch labs, quality control, testing labs

While both roles support biotech operations, a Biotech Manufacturing Associate primarily works on production and manufacturing processes in a cleanroom environment, focusing on assembling, monitoring, and maintaining manufacturing equipment. In contrast, a Laboratory Technician typically conducts experiments, tests, and quality control procedures in a laboratory setting. Both roles require attention to detail and adherence to safety protocols, but their daily tasks and work environments differ significantly.

What job categories do people searching Biotech Manufacturing Associate jobs in Sandy, UT look for?

The top searched job categories for Biotech Manufacturing Associate jobs in Sandy, UT are:

What cities near Sandy, UT are hiring for Biotech Manufacturing Associate jobs?

Cities near Sandy, UT with the most Biotech Manufacturing Associate job openings:

Biotech Manufacturing Associate jobs near you
Infographic showing various Biotech Manufacturing Associate job openings in Sandy, UT as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $41,185 per year, or $19.8 per hour.

MS&T Engineer/ Associate Scientist/ Scientist

Ratio Therapeutics, Inc.

West Valley City, UT • On-site

$90K - $130K/yr

Full-time

Re-posted 17 days ago

Key responsibilities

  • Author and execute technology transfer and validation documentation, including protocols, risk assessments, and summary reports.

  • Oversee process validation strategies, including process qualification, continued process verification, and lifecycle management activities.

  • Support optimization, characterization, and scale-up of radiopharmaceutical manufacturing processes.

Job description

About Ratio Therapeutics
Ratio Therapeutics is committed to improving and extending the lives of cancer patients without sacrificing their quality of life. We are a team of passionate scientists, engineers, and business professionals dedicated to advancing the field of targeted radioligand therapy. To accomplish this, we utilize our proprietary TRILLIUM™ and MACROPA™ platforms: TRILLIUM™ allows fine-tuning of radioligand pharmacokinetics thereby enhancing the therapeutic index, while MACROPA™ simplifies the manufacturing process for the alpha-emitting isotope, actinium-225. These enabling platform technologies have resulted in an emergent pipeline of novel therapeutic candidates. We are looking for talented, dedicated, and creative individuals eager to help us advance these technologies from discovery research through clinical development. Join us in our quest to become the leading innovator in radioligand therapy and improve the lives of cancer patients and their families.
About the Position
Ratio is seeking an MS&T Associate Scientist/Scientist to support the buildout and phased expansion of our new radiopharmaceutical manufacturing facility in the Salt Lake City metropolitan area (West Valley City, Utah) and to support GMP manufacturing operations once the site is operational. The ideal candidate will enjoy working in a collaborative, fast-paced, multidisciplinary environment.
Initially, this role will focus on technology transfer and validation activities with emphasis on process validation and method validation. Over time, the MS&T Scientist will support ongoing technology transfers, lifecycle validation, periodic reviews of validated systems, change control impact assessments, and validation support for new projects and process introductions.
Key Responsibilities
  • Author and execute technology transfer and validation documentation, including protocols, risk assessments, summary reports, and related lifecycle documentation
  • Oversee process validation strategies including process qualification, continued process verification, and lifecycle management activities.
  • Perform technology transfer and validation activities in alignment with project schedules and site procedures.
  • Support optimization, characterization, and scale-up of radiopharmaceutical manufacturing processes.
  • Create, review, and revise related documents, including SOPs, validation plans, master plans, and protocols.
  • Lead and coordinate execution of validation and technology transfer activities
  • Lead periodic review activities for validated systems
  • Support change control through technology transfer, validation, and other required actions
  • Partner cross-functionally with internal departments, and external vendors to ensure compliant execution of technology and validation activities
  • Lead small to mid-sized projects and provide support for larger projects
  • Support manufacturing process readiness and train personnel in aseptic principles, manufacturing processes, and other programs as required.
  • Support regulatory inspections by the FDA, EMA, and other healthy authorities
  • Participate in quality systems activities, including change controls, CAPAs, deviations, and investigations

Required Qualifications
  • Bachelor's degree in Life Science, Engineering, or a related field
  • 5+ years of relevant technology transfer or validation experience in a GMP-regulated environment
  • 3+ years of experience with GMP aseptic manufacturing processes
  • Hands-on experience with process validation and lifecycle validation practices
  • Familiarity with risk-based validation principles and good documentation practices
  • Ability to work safely in a manufacturing environment
  • Strong organizational skills, attention to detail, and a practical, solution-oriented approach
  • Strong communication skills with the ability to clearly summarize technical topics for cross-functional audiences
  • Comfortable operating in a fast-paced environment with both strategic and hands-on responsibilities

Preferred Qualifications
  • Experience with digital validation platforms such as ValKit or Kneat
  • Experience supporting technology transfer and validation during facility startup or expansion
  • Experience in radiopharmaceutical, pharmaceutical, biotech, or other highly regulated manufacturing operations
  • Experience supporting change control, deviations, and validation impact assessments

The annual base salary for this role is expected to range between $90,000 and $130,000. This range is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. The actual base salary offered will depend on a variety of factors, including qualifications, work experience, skills, level of education attained, certifications or other professional licenses held, the location in which the applicant lives and/or from which they will be performing the job, and other job-related factors permitted by law.

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