• Data Review Scientist I - QC

• Location:

• Cincinnati, OH

• Pay:

• Up to $31/hour
• , based on experience

• Schedule:

• First Shift -
• 7:30 AM or 8:00 AM start

• Employment Type:

• Contract / Temp-to-Perm

• Contract Duration:

• Through
• September 30, 2027

• Work Setting:

• Onsite
• About the Opportunity
• Adecco Healthcare & Life Sciences is seeking a
• Data Review Scientist I
• to support quality control operations within a regulated laboratory environment in Cincinnati, Ohio. This role is ideal for a scientist with hands-on experience in
• chemistry, biochemistry, biology, microbiology, or analytical laboratory testing
• who has a strong eye for detail and enjoys evaluating scientific data for accuracy, completeness, and compliance. You will review analytical testing data associated with
• raw materials, in-process samples, finished products, and stability studies
• , while partnering closely with QC analysts, laboratory leadership, Quality Assurance, and other teams to identify and resolve discrepancies and support quality and product-release timelines.
• What You'll Do
• + Review analytical data, laboratory records, and supporting documentation generated by QC laboratories. + Evaluate data generated from analytical techniques such as
• HPLC, GC, spectroscopy, dissolution testing, and wet chemistry
• . + Verify calculations, results, specifications, instrument outputs, chromatograms, and supporting documentation for accuracy and completeness. + Ensure laboratory records comply with approved methods, specifications, SOPs,
• GMP requirements, and Good Documentation Practices (GDP)
• . + Identify and document errors, discrepancies, atypical results, and documentation deficiencies. + Partner with laboratory personnel to investigate and resolve data and documentation discrepancies. + Review testing data associated with
• raw materials, in-process materials, finished products, and stability samples
• . + Utilize laboratory information management systems (LIMS) and other electronic systems to review, document, and track analytical data and sample status. + Support investigations, deviations,
• OOS/OOT events
• , and other quality activities as assigned. + Maintain accurate, complete, and traceable records in accordance with data integrity requirements. + Collaborate with QC analysts, laboratory leadership, Quality Assurance, and cross-functional teams to support testing and product-release timelines. + Follow all applicable safety, quality, regulatory, and site procedures.
• What We're Looking For
• + •Bachelor's degree required•, preferably in •Chemistry, Biochemistry, Biology, Microbiology•, or a related scientific discipline.

+

• 2+ years of relevant laboratory experience preferred
• , particularly within pharmaceutical, biotechnology, life sciences, or another regulated environment. + Experience working in a
• QC, analytical, chemistry, biology, microbiology, or biochemistry laboratory
• . + Experience reviewing laboratory data or performing analytical laboratory testing strongly preferred. + Working knowledge of analytical techniques such as
• HPLC, GC, spectroscopy, dissolution testing, or wet chemistry
• . + Strong understanding of
• GMP, Good Documentation Practices, pharmaceutical quality standards, and data integrity principles

•. + Exceptional attention to detail with the ability to critically evaluate scientific data and identify discrepancies. + Strong analytical thinking and problem-solving skills. + Excellent organizational, written, and verbal communication skills. + Proficiency with Microsoft Office and laboratory information/electronic data systems. + Ability to work independently while collaborating effectively with laboratory and quality teams. + Ability to manage multiple priorities while maintaining accuracy and meeting deadlines.

• Why Consider This Opportunity?
• + •Up to $31/hour•, based on qualifications and experience.

+

• First-shift schedule
• with a 7:30 AM or 8:00 AM start. + Long-term contract opportunity
• through September 30, 2027
• . +
• Temp-to-perm potential
• for strong performers based on business needs. + Opportunity to build experience within a highly regulated
• pharmaceutical/life sciences quality environment
• . + Exposure to analytical testing, laboratory data review, GMP compliance, data integrity, investigations, and product-release activities. + Opportunity to collaborate with QC, Quality Assurance, laboratory leadership, and cross-functional scientific teams.
• Work Environment
• This is an
• onsite laboratory position in Cincinnati, Ohio
• . The role requires consistent first-shift availability and the ability to work effectively in a regulated laboratory environment.
• About Adecco Healthcare & Life Sciences
• Adecco Healthcare & Life Sciences connects qualified scientific, laboratory, healthcare, and life sciences professionals with opportunities across leading organizations. Eligible associates may have access to
• weekly pay, benefits, 401(k), skills training, and other resources
• based on assignment and eligibility.
• Adecco is an Equal Opportunity Employer.

• Pay Details:

• $28.

00 to $31.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to https://www.adecco.com/en-us/candidate-privacy The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: + The California Fair Chance Act + Los Angeles City Fair Chance Ordinance + Los Angeles County Fair Chance Ordinance for Employers + San Francisco Fair Chance Ordinance

• Massachusetts Candidates Only:

• It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment.

An employer who violates this law shall be subject to criminal penalties and civil liability.