Associate Scientist R D

Position: Associate Scientist I   R D
** 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…