MVA Scientific Consultants is a small analytical laboratory working with pharmaceutical, medical device, environmental, and manufacturing companies (among others) seeking a Quality Manager to lead our Quality Systems Program. We are ISO 17025 certified and cGMP compliant. The responsibilities of this position include oversight of the quality program, ensuring that the requirements of cGMP and ISO 17025 are met. This will be a hands-on job, making sure that all of the record keeping, reporting, maintenance and calibration functions are carried out promptly and properly, implementing and ensuring compliance with procedures and protocols, scheduling and conducting quality training, and addressing corrective action/preventive action activities and effectiveness. The position includes responsibility for internal audits and reporting and interfacing with external auditors from our clients, the FDA and our ISO certifying body. The Quality Manager will work closely with scientists and management to execute his or her duties.
The ideal candidate will be highly organized and have experience implementing and enforcing a quality program in an analytical environment. Part-time or flexible scheduling will be considered for the right candidate.
About MVA Scientific Consultants
MVA Scientific Consultants is a full-service laboratory offering customized analytical testing, investigative analysis and ongoing R&D support to a wide variety of industries, including pharmaceutical, environmental, and industrial hygiene, among others. We help our clients solve problems and answer questions, and we pride ourselves on providing high quality service in a timely manner. We are ISO/IEC 17025 accredited, cGMP compliant, and FDA registered. MVA was founded in 1990 and maintains a staff of 18 to 20 people. We provide a flexible, family-friendly environment. Additional benefits include health insurance, a 401(k) with company matching, and paid vacation and sick time.
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