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Per Diem Qc Data Reviewer Jobs (NOW HIRING)

GMP Data Reviewer (Pharma)

Oakdale, MN

$55K - $65K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Compensation: $55,000 - $65,000 per year The salary for this position reflects a variety of factors ... or quality control data, standard operating procedures (SOPs), quality exceptions, logbooks ...

Assists with QC's data management, including data review and trending. * Maintains specific QC files and database records for process and/or quality improvement efforts. * Maintain laboratory ...

Perform medical record abstraction including data entry into tool, overread, and quality review using applicable HEDIS, State, and project-specific technical specifications. * Apply structured ...

... review and validation of approximately 200 analytical procedures and methods, and regular monitoring, trending, and reporting of QC data to support product quality and continuous improvement.

New

Quality Control Analyst

Rensselaer, NY · On-site

$64K - $97K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

Review analytical QC data, compile trend reports, and provide technical summaries to management to ensure manufacturing accuracy. • Audit Readiness: Maintain a pristine, compliant workspace and ...

The QC Manager leads a team of QC reviewers responsible for data verification, review of assay outputs, documentation accuracy, and compliance across all GLP bioanalytical studies. Key ...

Quality Assurance Technician

Cambridge, MA

$30 - $40/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Verify and approve Quality Control (QC) data accurately and in a timely manner. * Review batch records thoroughly and ensure a complete and accurate chain of custody for all materials and ...

Data Center Construction QA/QC Manager

Amarillo, TX · On-site

$140 - $190/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... review to L1-L5 commissioning and turnover. Working closely with Energy Marshals and key ... Travel Expense Reimbursements & Per Diem (per company policy) Applicants must be currently ...

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Per Diem Qc Data Reviewer information

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$12

$26

$43

How much do per diem qc data reviewer jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for per diem qc data reviewer in the United States is $26.24, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $36.30 per hour, depending on experience, location, and employer.

What is a per diem QC data reviewer?

A Per Diem QC (Quality Control) Data Reviewer is a professional who works on a flexible, as-needed basis to review and verify data in quality control processes, often within pharmaceutical, biotechnology, or laboratory environments. Their main responsibility is to ensure the accuracy, completeness, and compliance of laboratory data with regulatory standards and company procedures. They may review test results, documentation, and reports to identify discrepancies or errors that could impact product quality or regulatory compliance. Per diem positions offer flexibility and are often used to support high workloads or special projects. These roles are critical in maintaining data integrity and ensuring that products meet required quality standards.

What are the key skills and qualifications needed to thrive as a per diem QC data reviewer?

To thrive as a Per Diem QC Data Reviewer, you need strong analytical abilities, attention to detail, and a background in life sciences or a related field, often supported by a bachelor's degree. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practice (GMP) regulations, and relevant data review software is typically required. Excellent organizational skills, effective communication, and the ability to work independently are valuable soft skills for this role. These competencies ensure accurate data review, regulatory compliance, and reliable quality control in pharmaceutical or biotechnology environments.

What are some common challenges faced by per diem QC data reviewers and how can they be addressed?

Per Diem QC Data Reviewers often face challenges such as managing fluctuating work volumes, adapting to varying protocols across projects, and maintaining accuracy under tight deadlines. Since the role is typically flexible or on-call, time management and the ability to quickly familiarize oneself with new datasets or procedures are essential. To address these challenges, it helps to develop strong organizational skills, maintain up-to-date knowledge of quality standards, and communicate proactively with project managers and laboratory teams to clarify expectations and resolve discrepancies efficiently.

What is the difference between Per Diem Qc Data Reviewer vs Per Diem Data Coordinator?

AspectPer Diem Qc Data ReviewerPer Diem Data Coordinator
CredentialsTypically requires a degree in life sciences or related field, with experience in data reviewOften requires similar educational background, with focus on data management skills
Work EnvironmentWorks in clinical trial settings, reviewing data for accuracy and complianceManages data entry, organization, and coordination across trial sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsResearch organizations, clinical trial sponsors, CROs

The Per Diem Qc Data Reviewer primarily focuses on reviewing clinical data for quality and accuracy, while the Per Diem Data Coordinator handles data management and coordination tasks. Both roles require similar educational backgrounds and work within the clinical research industry, but their daily responsibilities differ significantly.

More about Per Diem Qc Data Reviewer jobs

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What are the most commonly searched types of Qc Data Reviewer jobs?

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The top searched job categories for Per Diem Qc Data Reviewer jobs are:

Infographic showing various Per Diem Qc Data Reviewer job openings in the United States as of August 2026, with employment types broken down into 78% Full Time, and 22% Contract. Highlights an 100% In-person job distribution, with an average salary of $54,583 per year, or $26.2 per hour.

$55K - $65K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 10 days ago


Job description

Shift:

Monday through Friday, 8:30 AM - 5:00 PM

Are you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives.

This is a full-time, onsite, GMP Data Reviewer position located in Oakdale, MN, Monday through Friday, 8:30 a.m. - 5:00 p.m.

Compensation: $55,000 - $65,000 per year

The salary for this position reflects a variety of factors. Compensation will be determined based on the candidate’s geographic location, relevant experience, education, skills, and alignment with internal equity. Market conditions, budgetary considerations, and organizational compensation guidelines may also influence the final offer. 

Make an Impact. Build a Career.

Pace® Life Sciences delivers a comprehensive suite of contract CMC development, CTM manufacturing, regulatory compliance, consulting, and facility support services to the pharmaceutical, biopharmaceutical, and gene therapy industries. Operating across a network of CDMO sites, GMP analytical testing laboratories, and manufacturing support centers, we partner with clients to efficiently advance programs from early development through commercialization.

Our experienced industry experts and continued investment in state-of-the-art facilities reflect our commitment to quality, speed, and reliability. United by a shared purpose, we bring meaningful value to patients, healthcare professionals, and health businesses worldwide by delivering services that support a safer, healthier future.

ESSENTIAL FUNCTIONS 

This class specification lists the major duties and requirements of the job and is not all-inclusive. Incumbent(s) may be expected to perform job-related duties other than those contained in this document and may be required to have specific job-related knowledge and 

skills. 

  • Overseeing, reviewing, writing, updating, completing, and processing quality forms, documents, databases, and related materials and information.  This includes, but is not limited to manufacturing batch records, technical records, pertinent laboratory or quality control data, standard operating procedures (SOPs), quality exceptions, logbooks, tracking systems and LIMS data/reports. Data and records may be in the form of electronic or paper records or laboratory notebooks. 

  • Provides intermediate to complex analysis, interpretation and counsel to staff, management, and functional leaders regarding quality policies, programs, and practices; involves varied operations and leading implementation and change. 

  • Provides various research, feedback, and decisions to resolve management and employee questions and requirements; assists with receiving customer feedback and coordinating resources and responses as required. 

  • Analyzes and reviews intermediate to complex operations, results, feedback, and related quality information on an ongoing to as needed basis to determine trends, draw conclusions, interpret findings, and presents results, proposals, and recommendations to management. 

  • Ensures the accuracy of various tests, equipment, actions, procedures and operational databases, reports, and related details through audits, queries, and operational reviews; works with teams to resolve discrepancies. 

  • Assists with developing or participating in quality or cross-functional project or program objectives, which includes proposed budgets, timelines, materials, personnel, and other project requirements, receives direction, and presents information to management. 

  • Interprets and applies department policies and procedures and assists with applicable laws, rules, and regulations; receives guidance within these areas as needed. 

  • Contributes to the efficiency and effectiveness of the department's service to its customers by offering suggestions and directing or participating as an active member of a work team. 

  • Promotes and supports the overall mission of Pace Analytical by demonstrating courteous and cooperative behavior when interacting with customers and staff; acts in a manner that promotes a harmonious and effective workplace environment.  

QUALIFICATIONS 

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. 

Education and Experience 

Bachelor's degree in chemistry, operations, or a closely related field; AND two to four (2-4) years of quality experience, including experience with complex programs or operations; OR an equivalent combination of education, training, and experience. 

Required Knowledge and Skills 

Required Knowledge 

  • Intermediate to complex principles, practices, and techniques of quality. 

  • Various understanding of the administration and oversight of quality programs, policies, and procedures. 

  • Intermediate to complex methods to resolve quality problems, questions, and concerns. 

  • Various understanding of applicable quality laws, codes, and regulations. 

  • Understanding of various testing tools, equipment, and calibration. 

  • Computer applications and systems related to the work. 

  • Principles and practices to serving as an effective project team member. 

  • Methods to communicate with staff, coworkers, and customers to ensure safe, effective, and appropriate operations. 

  • Correct business English, including spelling, grammar, and punctuation. 

Required Skills 

  • Performing intermediate to complex professional-level quality duties in a variety of assigned areas. 

  • Overseeing and administering comprehensive and varied quality functions. 

  • Training others in policies and procedures related to the work. 

  • Serving as a team member and the development and management of projects. 

  • Operating in a both a team and individual contributor environment. 

  • Interpreting, applying, and explaining applicable laws, codes, and regulations. 

  • Preparing intermediate to complex functionals reports, correspondence, and other written materials. 

  • Using initiative and independent judgment within established department guidelines. 

  • Using tact, discretion, and prudence in working with those contacted in the course of the work. 

  • Performing effective oral presentations to large and small groups across functional peers and the department. 

  • Contributing effectively to the accomplishment of team or work unit goals, objectives and activities. 

  • Establishing and maintaining effective working relationships with a variety of individuals contacted in the course of the work. 

PHYSICAL/MENTAL REQUIREMENTS 

The physical demands described herein are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.  

 

Mobility to work in a lab and office setting, use standard office and lab equipment and stamina to sit for extended periods of time; exerting up to 20 pounds of force occasionally and/or up to 10 pounds of force frequently to lift, carry, push, pull or move objects; vision to read printed materials and computer screens; and hearing and speech to communicate in person or over the telephone.   

WORKING ENVIRONMENT 

Work is performed in a lab and office setting. Work is subject to chemicals, fumes, gases, noxious odors and related items in a lab setting.  

Find Your Place at Pace - We need you - your curiosity, your talents, and your drive - to help us advance this important work.

Benefits
When you join Pace®, you commit to work that makes a positive impact on our communities and our world. We commit to supporting you with benefits and perks that make a positive impact on your life. Full-time roles are eligible for our comprehensive benefits program which includes competitive salaries, medical, dental vision, 401K retirement savings plan (100% vested immediately in the employer match), life, disability and voluntary benefits, paid time off for holiday, sick and vacation days, HSA, wellness program, flexible spending accounts, tuition reimbursement, Employee Assistance program, parental leave, optional legal coverage and ID theft.

Equal Opportunity Employer

Pace® provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.