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Pharmaceutical Quality Control Reviewer Jobs (NOW HIRING)

System One

Joint Use QC Engineer

Hayden, ID · Remote

The QC Reviewer plays a key role in reviewing pole attachment applications, verifying compliance with utility specifications, and ensuring that engineering requirements are adhered to before ...

Adecco

QC Scientist I

Greenville, NC

$23 - $24/hr

Review test results and identify out-of-specification, unexpected, or non-routine results ... Knowledge of pharmaceutical quality and regulatory requirements, including GMP standards . * Strong ...

System One

Joint Use QC Engineer

Florence, AZ · Remote

The QC Reviewer plays a key role in reviewing pole attachment applications, verifying compliance with utility specifications, and ensuring that engineering requirements are adhered to before ...

Mountain Ltd.

Joint Use QC Engineer

Florence, AZ · On-site

The QC Reviewer plays a key role in reviewing pole attachment applications, verifying compliance with utility specifications, and ensuring that engineering requirements are adhered to before ...

Adecco

QC Scientist I

Greenville, NC

$23 - $24/hr

Review test results and identify out-of-specification, unexpected, or non-routine results ... Knowledge of pharmaceutical quality and regulatory requirements, including GMP standards . * Strong ...

System One

QC Analyst - 1st Shift

Bethlehem, PA · On-site

$28 - $35/hr

Perform peer review of raw analytical data and support routine stability and QC laboratory activities Requirements * Hands-on pharmaceutical Quality Control laboratory experience in a cGMP ...

System One

QC Analyst - 1st Shift

Bethlehem, PA · On-site

$28 - $35/hr

Perform peer review of raw analytical data and support routine stability and QC laboratory activities Requirements * Hands-on pharmaceutical Quality Control laboratory experience in a cGMP ...

System One

QC Analyst - 1st Shift

Bethlehem, PA · On-site

$28 - $35/hr

Perform peer review of raw analytical data and support routine stability and QC laboratory activities Requirements * Hands-on pharmaceutical Quality Control laboratory experience in a cGMP ...

System One

QC Analyst - 1st Shift

Bethlehem, PA · On-site

$28 - $35/hr

Perform peer review of raw analytical data and support routine stability and QC laboratory activities Requirements * Hands-on pharmaceutical Quality Control laboratory experience in a cGMP ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

TekWissen LLC

Quality Control Chemist

High Point, NC · On-site

Perform routine chemical and physical testing of pharmaceutical raw materials, packaging components ... Review analytical results and recognize out-of-specification (OOS), unexpected, or non-routine ...

Olon USA LLC

QC Associate Scientist

Painesville, OH · On-site

... pharmaceutical laboratory. This role is responsible for performing analytical testing of raw ... Review laboratory data for technical accuracy, completeness, compliance, and adherence to good ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract ... Perform batch release and stability testing for pharmaceutical products * Conduct assay ...

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Pharmaceutical Quality Control Reviewer information

See salary details

$30.5K

$81.3K

$129.5K

How much do pharmaceutical quality control reviewer jobs pay per year?

As of Sep 14, 2026, the average yearly pay for pharmaceutical quality control reviewer in the United States is $81,324.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $100,000.00 per year, depending on experience, location, and employer.

What does a pharmaceutical quality control reviewer do?

A Pharmaceutical Quality Control Reviewer is responsible for reviewing laboratory data, test results, and documentation to ensure that pharmaceutical products meet quality and regulatory standards. They verify that processes and results comply with Good Manufacturing Practices (GMP) and internal protocols. Their work helps to ensure the safety, efficacy, and consistency of medications before they reach the market. Additionally, they may identify deviations, recommend corrective actions, and collaborate with laboratory staff to maintain high-quality standards.

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

To thrive as a Pharmaceutical Quality Control Reviewer, you need a strong background in chemistry, biology, or pharmacy, often supported by a relevant degree and experience in pharmaceutical quality assurance. Familiarity with analytical laboratory instruments, Good Manufacturing Practice (GMP) guidelines, and quality management systems is essential. Attention to detail, critical thinking, and effective communication are vital soft skills for this role. These capabilities ensure accurate review of laboratory data, compliance with regulatory standards, and the release of safe, high-quality pharmaceutical products.

What are some common challenges faced by pharmaceutical quality control reviewers, and how can they be addressed?

Pharmaceutical Quality Control Reviewers often encounter challenges such as tight deadlines for batch release, handling complex documentation, and staying updated with evolving regulatory standards. Managing large volumes of data while ensuring accuracy and compliance can be demanding. These challenges are best addressed by maintaining strong organizational skills, leveraging digital tools for documentation management, and participating in regular training sessions to keep current with industry regulations. Collaboration with laboratory analysts and regulatory affairs teams also helps in resolving discrepancies efficiently.

What is the difference between Pharmaceutical Quality Control Reviewer vs Pharmaceutical Quality Control Analyst?

AspectPharmaceutical Quality Control ReviewerPharmaceutical Quality Control Analyst
CredentialsBachelor's degree in pharmacy, chemistry, or related field; GMP trainingBachelor's degree in science or pharmacy; GMP knowledge
Work EnvironmentReview labs, documentation, and compliance reportsPerforming laboratory tests and data analysis
Employer & Industry UsagePharmaceutical manufacturing, quality assuranceLaboratories, quality control departments in pharma

The Pharmaceutical Quality Control Reviewer primarily evaluates and approves testing documentation, ensuring compliance with regulations, while the Pharmaceutical Quality Control Analyst conducts laboratory tests and analyzes data. Both roles require similar educational backgrounds and GMP knowledge, but their daily tasks differ—reviewers focus on documentation, analysts on testing. They work closely within pharmaceutical quality assurance teams to maintain product quality and compliance.

What are popular job titles related to Pharmaceutical Quality Control Reviewer jobs?

For Pharmaceutical Quality Control Reviewer jobs, the most frequently searched job titles are:

Infographic showing various Pharmaceutical Quality Control Reviewer job openings in the United States as of September 2026, with employment types broken down into 2% As Needed, 80% Full Time, 14% Part Time, 3% Contract, and 1% Nights. Highlights an 83% Physical, 1% Hybrid, and 16% Remote job distribution, with an average salary of $81,324 per year, or $39.1 per hour.

Joint Use QC Engineer

Hayden, ID • Remote

System One
Business Consulting Services • 5 - 10K employees
Learn more about System Oneexternal

Contractor

Re-posted 29 days ago

Job description

Mountain Ltd. is seeking an OSP Engineer to work Remotely! This will be working as a Permit/ROW QC Engineer.  
PA Quality Control Reviewer
Job Summary The Quality Control (QC) Reviewer is responsible for ensuring that all engineering standards from various third-party pole owners are met in the applications submitted by engineering vendors for joint-use projects. The QC Reviewer plays a key role in reviewing pole attachment applications, verifying compliance with utility specifications, and ensuring that engineering requirements are adhered to before applications are submitted for approval. This role also involves collaborating with the Quality Control Lead and escalating any issues with vendor submissions.
Essential Duties and Responsibilities The Essential Duties and Responsibilities listed below are a range of duties performed by the employee and not intended to reflect all duties performed:
  • QC Review of Applications: Conduct thorough reviews of pole attachment applications submitted by third-party engineering vendors. Ensure that the applications meet the specific engineering standards and utility requirements and comply with all QC Checklist.
  • Compliance with Utility Specifications: Verify that submitted applications adhere to utility-specific requirements, National Electrical Safety Code (NESC), and other relevant industry standards. Ensure correct cable attachments, clearance requirements, guying, and cabinet installations.
  • Standards Adherence: Ensure engineering standards regarding pole attachment, equipment placement, and guying specifications are followed, including bolt placements, horizontal clearances, vertical clearances, and adherence to restrictions for different pole types (e.g., wood, metal, fiberglass).
  • Communication and Escalation: Collaborate with the Lead QC Reviewer to address any issues or discrepancies found in vendor applications. Escalate vendor-related issues, especially regarding non-compliance or missed deadlines, to the Lead QC Reviewer.
  • Documentation and Reporting: Maintain detailed documentation of the review process and track any rejected applications or required corrections. Provide regular reports on application status, compliance issues, and vendor performance.
  • Continuous Improvement: Provide feedback to the engineering vendors and internal teams to improve the quality of future submissions. Help establish and maintain QC processes and QC Checklist to ensure consistent adherence to utility standards.
Qualifications/Skills
  • Technical Expertise: Strong understanding of joint-use pole attachment standards and utility engineering specification.
  • Reference Specification: Familiarity with NESC and other industry standards is required.
  • Detail-Oriented:  Ability to meticulously review and verify application details, ensuring they comply with utility requirements. Strong attention to detail in reviewing technical documents and pole attachment specifications.
  • Communication and Collaboration Skills: Excellent written and verbal communication skills to coordinate with engineering vendors and internal teams. Ability to escalate issues and provide clear, actionable feedback when discrepancies arise.
  • Problem Solving and Issue Resolution: Proven ability to identify non-compliance issues or discrepancies in engineering submissions and resolve them efficiently by collaborating with the Lead QC Reviewer and other stakeholders.
  • Vendor Management: Ability to manage relationships with third-party vendors, ensuring that engineering submissions meet quality standards and deadlines. Escalate non-compliance and missed deadlines to the Lead QC Reviewer when necessary.
Education and Experience
  • Minimum of three years of experience in quality control, utility joint-use, or engineering review processes, particularly in overhead distribution and pole attachment compliance.
  • Familiarity with utility specifications and industry standards.
  • NESC requirements are essential.
Physical Requirements
  • Ability to work for extended periods in a stationary position while consistently using computer systems for processing and submitting applications.
  • Frequent use of computers and technology devices for data management, application submittal, and project tracking.
They must:
  • QC Joint Use applications
  • Perform Make Ready reviews
  • Be able to markup/redline work prints
  • Have used Alden and/or NJUNS or other pole owner systems
  • Have experience using SalesForce or similar CRM
  • Be able to review Pole load analysis
 Preferred experience:
  • IQGEO
  • Katapult
Shape the future. Summit success. Join our team and become part of a legacy that has been at the forefront of engineering excellence since 1979. Thank you for your interest in Mountain Ltd. For more career opportunities, please visit us at www.mountainltd.com #M4  

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About System One

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System One helps employers get work done more efficiently and economically without compromising quality. Over our 35+ year history, we've helped connect thousands of talented people with innovative companies. The excitement of a perfect fit motivates us every single day.

Industry

Business consulting services and recruiting and staffing services

Company size

5,001 - 10,000 Employees

Headquarters location

Pittsburgh, PA, US

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