QC Analyst II

Location: West Chester, OH

Type: Contract-to-Hire

Department: Quality Control

Hourly Pay Rate: $32-$34 Kelly Science is seeking an Analyst II, QC Chemistry to join a quality control laboratory supporting pharmaceutical manufacturing operations. This role is responsible for performing analytical testing, maintaining laboratory equipment, supporting investigations, and ensuring compliance with cGxP and quality standards. This is a contract-to-hire opportunity with an opening only on night shift, rotating schedule. Night Shift 2-2-3 rotating 12-hour schedule 6:00 PM – 6:00

AMKey Responsibilities: Perform analytical testing on samples including finished products, raw materials, stability, in-process, and water samples Operate, maintain, and troubleshoot laboratory equipment and instrumentation Support laboratory investigations and assist with resolving deviations or out-of-specification results Execute laboratory protocols to support validation, method development, and method transfer activities Review QC data to ensure accuracy and compliance with quality standards Assist with updates to laboratory methods and Standard Operating Procedures (SOPs)Identify and recommend opportunities for continuous improvement in laboratory processes Work collaboratively with Quality Control, Quality Assurance, and manufacturing teams Safely handle chemicals and hazardous materials according to established safety procedures Maintain compliance with cGxP requirements and regulatory standards Support environmental monitoring activities as needed, including data review and sample collection within manufacturing areas

Qualifications: Required Working knowledge of cGxP requirements and laboratory quality practices Strong analytical and problem-solving skills Basic knowledge of laboratory techniques, statistics, and quality control terminology Strong written, verbal, and organizational skills Ability to adapt quickly in a fast-paced laboratory environment Preferred Bachelor’s degree in Chemistry, Biology, or related scientific field Prior QC laboratory experience in the pharmaceutical or biotech industry Experience with analytical instrumentation such as HPLC