Job Title Sr. Manager Quality Control Job Description Business: Pharma Solutions Department: Analytical Quality Control (AQC) Location: Lexington Job Overview Reporting to the Director of Quality, the Sr. Manager, Quality Control has responsibility for the Analytical and Microbiology Quality Control (AQC/MQC) laboratories. The position will provide strategic direction and leadership to improve quality, efficiency, process standardization, and capabilities of the Quality Control Department. Reporting Structure This position reports to the Director of Quality. Key Responsibilities: • Direct oversight of activities performed within Quality Control Laboratories • Monitor revenue goals ensuring that Laboratories meet or exceed expectations • Develop and manage department budgets • Regularly monitor applicable internet and written information published by US FDA, EMA, PMDA, Other Applicable Agencies as required, and pharmaceutical manufacturing and laboratory technology organizations for the purpose of review/incorporation of latest requirements and guidelines into routine PPS laboratory operations • Establish short and long-range plans for the timely and efficient execution of the testing activities within scope of the business priorities and applicable regulatory requirements (FDA, OSHA, etc.) • Apply necessary oversight to the stability study program and ensure current regulatory guidelines are followed • Oversee laboratory instrumentation activities including procurement, qualification, preventative maintenance, and calibration • Establish, implement, and manage Laboratory Programs and/or Policies, SOPs, and good record keeping practices that are compliant with current regulatory requirements • Oversee all quality investigations within the departments (deviations, CAPA and LIR) • Ensure Lab is a constant state of compliance and Sustains Permanent Inspection Readiness (PIR) • Ensure suitable laboratory safety procedures are in place • Ensure that there is a department training program in place so that department staff are continuously developing and are current with industry practice • Ensure that department technical expertise and capabilities are constantly evolving and current with industry. • Provides information regarding Quality Control systems and data to internal or external regulatory personnel during inspections or inquiries • Analyse and trend sample results and perform statistical studies and evaluations of key performance indicators • Develop mechanisms and structures to allow for adjustment in the laboratory testing schedules to meet changing priorities due to business needs. • Serve as liaison with the corporate data, documentation, and review center. • Interact directly with project managers, clients, consultants, and regulatory agencies • Oversee the development, execution and implementation of quality improvement plans within the QC Department • Oversee the identification, procurement, qualification and implementation of new laboratory equipment, and software platforms (i.e. LIMS, Empower, etc.) as needed • Perform gap assessments and implement CAPAs as needed • Support internal and external audits, agency inspections, responses and CAPAs • Support Cross Functional Quality and Operational activities/projects as needed • Create and support an environment where department members seek opportunities to improve current practices in terms of quality, efficiency and safety • Lead and develop/mentor QC members • Assign department resources so that company goals/timelines are achieved Qualifications: • B.A. or B.S in scientific related field, Biology, Life Science, Chemistry, or related scientific discipline preferred • Minimum of ten (10) years' progressive experience in a regulated cGMP industry is required, with five (5) years' management experience • Must have experience working within a GMP parenteral/sterile manufacturing environment, contract manufacturing a plus • Strong/demonstrated knowledge of cGMP regulations • Possess excellent technical writing and oral communication skills • Six Sigma Green Belt, Benchmarking and Project Management experience preferred • Ability to travel as needed. • Minimum of ten (10) years' progressive experience in a regulated cGMP industry is required, with five (5) years' management experience • Must have experience working within a GMP parenteral/sterile manufacturing environment, contract manufacturing a plus • Strong/demonstrated knowledge of cGMP regulations • Possess excellent technical writing and oral communication skills