Job Title: Data ReviewerJob Description

The Data Reviewer plays a vital role in ensuring the delivery of safe and effective medicines by maintaining the accuracy, integrity, and compliance of laboratory and manufacturing data. This position involves conducting technical reviews of analytical and laboratory data associated with raw materials, in‑process, and finished product testing at a biopharmaceutical manufacturing site. The reviewer verifies that all data meet cGMP, FDA, DEA, and ICH regulatory standards prior to batch disposition and release.

ResponsibilitiesPerform independent technical review of laboratory data from physical, dimensional, chemical, and instrumental testing to ensure compliance with approved specifications and procedures.Review analytical results, including visual inspections, titrations, pH, UV/Vis, HPLC, GC, AA, and other applicable techniques.Verify data integrity, calculations, documentation completeness, and adherence to cGMP and data governance standards prior to product or material release.Enter, review, and approve results within laboratory information management systems (LIMS) and associated documentation systems.Prioritize data review activities based on production needs, turnaround goals, and FIFO principles, in coordination with supervisors or data coordinators.Identify, document, and escalate atypical results, deviations, or compliance concerns; support investigations and change control activities as required.Support laboratory safety, inspection readiness, and regulatory compliance by adhering to site policies and applicable regulatory requirements.Provide technical guidance, training, or subject‑matter support to analysts and peers as appropriate for the role level.Essential SkillsMinimum of 2 years of GMP Data Review experience in QC chemistry labs.Proficiency with laboratory information management systems (LIMS) and Empower.Working knowledge of cGMPs and regulated laboratory practices.Experience reviewing or generating analytical laboratory data.Strong attention to detail, documentation accuracy, and data integrity.Effective written and verbal communication skills.Additional Skills & QualificationsBachelor’s degree in Chemistry, Biology, Microbiology, or related life science field, OR Associate degree with relevant laboratory or quality experience, OR High school diploma (or equivalent) with significant relevant experience.Prior experience in a Quality Control or pharmaceutical laboratory environment.Ability to work independently in a fast-paced manufacturing environment.Work Environment

The position operates on a Monday to Friday, 1st shift schedule with a 40-hour work week. The office space is located above the lab, and the role requires on-site presence.

Job Type & Location

This is a Contract position based out of Greenville, NC.

Pay and Benefits

The pay range for this position is $40.00 - $70.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Greenville,NC.

Application Deadline

This position is anticipated to close on Feb 26, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.