Kelly Scientific Resources (KSR) is a specialty service of Kelly Services, Inc., a leader in providing workforce solutions. Since its launch in 1995, KSR has provided staffing and placement services to a broad spectrum of industries, including biotechnology, chemical, consumer products, cosmetics, environmental, food sciences, medical/clinical, pharmaceutical, and petrochemical. Today, KSR leads the world in dedicated scientific and clinical research staffing. Visit www.kellyscientific.com to learn more and view a full listing of our opportunities. Microbiologist - 1 year contract Responsibilities: Primary role is to perform micro testing of raw materials, semi-finished and finished products, cleaning validation samples and complaint samples within standard times. This will include setting up tests using aseptic techniques, transfers and reading plates. Maintain QC laboratory equipment performance: perform assigned laboratory duties; maintain equipment according to SOPs & manufacturers’ guidelines; Maintain quality results: perform tests according to quality & customer service standards; document results according to cGMP standards; assist in investigations of OOS results by problem solving & troubleshooting; write minor deviations; ensure compliance to cGMP; write investigation reports; assist in regulatory & corporate audits; conduct & participate in self-inspections.. Complete operational requirements as per schedule: attend Production Coordination/Value Stream Daily Meetings; support process validation; implement efficiencies to improve productivity; review QC procedures; implement new procedures; maintain QC laboratory supplies inventory. Implement new programs, tests methods, instrumentation, & procedures: prepare proposals; initiate change proposals; write justifications & feasibility reports; perform parallel testing; evaluate new methods. Maintain a safe & healthy work environment: follow all safety policies; maintain a clean & orderly work area; report any potentially unsafe conditions within the workplace. Perform all work according to cGMP and following regulatory and standards, including thorough documentation and prompt reporting of any anomalies Follow all safety policies and maintain a clean and orderly work area May be required to work shifts Qualifications: University Degree or College Diploma in Microbiology Minimum of 2 years Quality Control microbiology experience in pharmaceutical laboratory environment Good theoretical and practical knowledge of microbiological techniques Knowledge of Microbial IDs and investigations Demonstrated computer proficiency LIMS, SAP and Excel Good knowledge of laboratory GMP and the Pharmacopoeias. Good verbal and written communication skills Works well in a fast-paced team environment and individually Ability to manage multiple projects and tasks concurrently and effectively