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New · posted Oct 15

Tolmar · Pharmaceuticals

QC Data Reviewer II (2nd Shift)

  • Fort Collins, CO
  • On-site
  • Full-time
  • Senior & Principal
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Pay$67K–$71Ka year · $32.00–$34.00 an hour
EmploymentFull-time
LocationFort Collins, COOn-site
LevelSenior & Principal
FunctionQuality ControlQuality
Deadline

Open until filled

The role

Purpose and Scope

Perform data review to ensure the quality of laboratory data is maintained in accordance with the highest standards. Ensure that all data generated is documented according to cGMP and ALCOA+, and maintain data integrity.  Data review will encompass review against all applicable methods, work instructions and standard operating procedures.

What you need

  • Bachelor’s Degree in science or related field.
  • Two or more years of analytical laboratory experience and/or data review in a pharmaceutical environment.

Knowledge, Skills & Abilities

Knowledge

  • Experienced in the operation of analytical laboratory instruments such as HPLC, GC, FTIR, pH, GC, UV-Vis spectrophotometry, TLC, Karl Fischer titration, rheometry.
  • Experience with sample preparation from a variety of matrices.
  • Working understanding of FDA regulations, USP, NF, ICH, EP, and other pertinent compendia.
  • Experience in the accurate review of laboratory testing data.
  • Experience with laboratory and wet chemistry techniques (e.g. weighing, volumetric glassware, titrations, etc.).
  • Effective written and oral communication skills.
  • Experience with the use of electronic document management system(s).
  • Experience with the use of a LIMS system preferred.
  • Experience with the use of word processing, spreadsheet, and database programs, including MS Office.
  • Experience with computer systems for sample tracking, laboratory equipment, and raw data handling.

Abilities

  • Ability to learn and apply new techniques.
  • Attention to detail. Accurate and consistent in data compilation and review.
  • Ability to work independently, with other analysts, and handle multiple projects and timelines concurrently.
  • Ability to identify process inefficiencies and correct them.
  • Experience with electronic notebook administration a plus.

Skills named in this posting

What you'll do

  1. Perform data review to ensure compliance with published methods, work instructions, compendia, and other standard operating procedures.
  2. Evaluate testing results and data against relevant specifications and suitability requirements.
  3. Ensure that all data generated follows the principles of ALCOA + and recognize discrepancies related to testing documentation.
  4. Perform review of logbooks, materials, equipment calibration and instrument settings.
  5. Review all applicable data printouts including, titration and other wet chemistry printouts, chromatography, integration and sequences.
  6. Review and approve all audit trails and any associated metadata applicable to the testing and data generated. Work to resolve any discrepancies that are found.
  7. Generate standard forms for testing to ensure consistency across all types of testing.
  8. Perform routine calculations.
  9. Review daily verifications generated in the laboratory.
  10. Review and approve sample submission paperwork.
  11. Authorize all sample data in the notebook as well as the associated data repositories (Endeavor and LIMS).
  12. Perform review of chemist reports generated in the laboratory.
  13. Attend required company and department meetings.
  14. Complete required training activities within required timeframes.
  15. Assist with training of other analysts and reviewers.
  16. Assist with review and preparation of standard operating procedures and training documents.
  17. Foster cooperation and teamwork among staff.
  18. Following policies, protocols, and standard operating procedures.
  19. Ensure testing per deviations and laboratory investigations was followed.
  20. Participate in laboratory process improvement initiatives such as lean lab principles, implementation of electronic laboratory notebooks and ERP systems.
  21. Participate in required annual hazardous waste training. Hazardous waste involvement may include but is not limited to container and tank management and inspections, generation of hazardous waste as a part of production or sampling processes, and transfer of hazardous waste between lab procedure area, satellite accumulation, and storage. Responsible for daily activities and supervising staff that are hazardous waste generators and/or handlers. Respond to spills according to the Chemical Spill Response procedure.
  22. Perform other duties as assigned.

Pay and benefits

$66,560 – $70,720 a year

Employer provided

$32.00 – $34.00 an hour · yearly at 2,080 hours (40 a week)

How this compares

Tolmar compensation programs are focused on equitable, fair pay practices including market-based base pay and a strong benefits package. The final compensation offered may vary from the posted range based on the selected candidates qualifications and experience.

  • Shift differential $1.50 per hour

Where you'll work

Fort Collins, COOn-siteOpen in Maps (opens in a new tab)

More jobs in Fort Collins, CO

Working conditions

Core Hours: Core Hours: Monday - Friday, 3:00 pm - 11:30 pm

  • Training Hours may vary 
  • Laboratory setting: may be exposed to solvents, bio-hazardous materials, hazardous waste, and pharmaceutical substances.
  • Office setting.

From the posting

About Tolmar

Core Values

  • The QC Data Reviewer II is expected to operate within the framework of Tolmar’s Core Values:
    • Center on People:  We commit to support the well-being of our patients. We are committed to treating our employees and those we serve as valued partners. By placing people at the heart of our actions, we actively engage, invigorate, acquire knowledge, and grow together.
    • Are Proactive & Agile:  We embody a culture of engagement and action. With a hands-on approach, we fearlessly adapt to change. We anticipate, respond swiftly and efficiently to ignite a spirit that propels us towards extraordinary outcomes.
    • Act Ethically:  We are committed to consistently conducting our business in an ethical, compliant, and socially aware manner, in line with our purpose of positively impacting lives. We actively cultivate diversity, equity, inclusion & sustainability in our workplace.
    • Constantly Improve:  We are committed to a collaborative & proactive effort to improve our products, systems, processes, and services by reducing waste, increasing efficiency & improving quality.
    • Are Accountable:  We think, act, and communicate with honesty, transparency, and clarity in alignment with our core values. We don't compromise our values for near term gain. We take accountability & ownership of our work, actions, successes, and setbacks. We strive to deliver our best as we shape the future.
Tolmar company page · 9 open roles
Equal opportunity, accessibility and legal noticesTolmar's statements, word for word

Tolmar is an Equal Opportunity Employer. We do not discriminate on the basis age 40 and over, color, disability, gender identity, genetic information, military or veteran status, national origin, race, religion, sex, sexual orientation or any other applicable status protected by state or local law. It is our intention that all qualified applicants be given equal opportunity and that selection decisions are based on job-related factors.

Job intelligence

The context around this role

Live data · October 15, 2026

Salary intelligence

How the pay compares

This role's midpoint is 28% below the US median for Quality Control roles at this level.

This roleEmployer provided

$66,560 to $70,720 a year

Senior & Principal roles in the US49 roles publishing pay

Middle half $78,500 to $108,500, median $95,000
Annual base pay
Annual base payLowMedianHigh
This role$66,560—$70,720
All US$78,500$95,000$108,500

This role: Tolmar's own published range, converted to a year at 2,080 hours. Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, October 15, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Quality Control

The general path across 275 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not Tolmar's own promotion track.

  1. One step back

    Associate & Specialist

    Often: Quality Inspector · Quality Control Inspector

    $60K median149 open

  2. This role

    Senior & Principal

    Often: Scientist, Quality Control · Senior Scientist, Quality Control

    $95K median70 open

  3. Next step

    Manager

    Often: Quality Control Manager · Manager Quality Control

    $127K median31 open

  4. Later

    Director

    Often: Associate Director, Quality Control · Senior Director, Quality Control

    $199K median25 open

Skills DNA

What this role leans on

How many of the posting's 42 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 5 linesLab testing and methods: 20 linesDocumentation and SOPs: 8 linesInvestigations and CAPA: 1 lineRegulatory submissions: 1 lineQuality systems and risk: 1 lineData and digital systems: 4 linesCollaboration and leadership: 7 linesGMPLab testingDocumentationInvestigationsSubmissionsQuality systemsData systemsTeamwork
  • Lab testing and methods20
  • Documentation and SOPs8
  • Collaboration and leadership7
  • GMP and compliance5
  • Data and digital systems4
  • Investigations and CAPA1
  • Regulatory submissions1
  • Quality systems and risk1

Regulatory intelligence

The rules behind this role

Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.

From Regulatory News

Manufacturing and quality coverage for this profession

Company hiring pulse

Tolmar on Regulatory Jobs

9
Open roles
8
Distinct roles
2
Locations

By discipline

  • Quality8 89%
  • Compliance & Safety1 11%

By level

  • Senior & Principal4 44%
  • Associate & Specialist4 44%
  • Manager1 11%
See all 9 Tolmar roles

More roles at Tolmar

All 9 Tolmar roles

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QC Data Reviewer II (2nd Shift) at Tolmar

Open until filled. $67K–$71K a year, employer provided.

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    QC Data Reviewer II (2nd Shift) at Tolmar — Fort Collins, CO | Regulatory Jobs