What are the responsibilities and job description for the Quality Control Microbiology Data Reviewer position at Conperio Technology Solutions?
Quality Control Microbiology Reviewer (Contract – 6 Months)
Location: Lexington, KY (On-site)
All candidates must be able to show proof of being a U.S. Citizen or Green Card Holder.
Local candidates to the Lexington, KY area required.
Project’s estimated term is for 6 months.
About Conperio
Conperio is a trusted technology and staffing partner with over 34 years of experience supporting manufacturers and life sciences organizations in highly regulated environments. In addition to delivering smart manufacturing and digital transformation solutions, Conperio operates a dedicated staffing organization that places top talent with premier customers across quality, engineering, IT, and manufacturing disciplines.
Role Summary
Conperio is seeking a Quality Control Microbiology Data Reviewer to support a 6-month contract assignment at one of our premier customer locations in Lexington, KY. This role is responsible for the detailed review of QC Microbiology laboratory data to ensure accuracy, integrity, and compliance with internal methods, SOPs, and external regulatory requirements, including cGMP, FDA, ICH, and pharmacopeial standards.
Key Responsibilities
- Conduct thorough and timely reviews of raw data, laboratory notebooks, and supporting documentation for raw materials, in-process samples, finished products, and stability samples
- Review microbiological testing associated with USP <61>, <62>, <51>, <788>, and Purified Water testing for completeness and adherence to approved methods
- Ensure documentation complies with ALCOA principles and Good Documentation Practices (GDP)
- Collaborate directly with microbiologists to resolve data discrepancies, incomplete records, and documentation issues
- Review audit trails for computerized systems to confirm data integrity and proper system usage
Qualifications
- Bachelor’s degree in Microbiology, Biology, or a related life science field
- 2–5 years of experience in a pharmaceutical or QC laboratory environment, including laboratory data review
- Required experience with USP <61>, <62>, <51>, <788>, and Purified Water testing
- Strong understanding of cGMP, GDP, and data integrity principles
- Knowledge of FDA and ICH regulatory guidelines
- Exceptional attention to detail and strong written and verbal communication skills
- Ability to manage multiple priorities independently while working collaboratively with a team
Physical Requirements
- Regular use of hands for handling materials and supplies
- Extended computer use and electronic communication
- Ability to stand and walk for extended periods
- Occasional lifting of up to 20 pounds
- Ability to wear appropriate PPE and follow all site safety procedures
Pay: $18.00 - $23.00 per hour
Benefits:
- Dental insurance
- Health insurance
- Retirement plan
- Vision insurance
Work Location: In person
Salary : $18 - $23