Job Description:
The end client is unable to sponsor or transfer visas for this position; all parties authorized to work in the US without sponsorship are encouraged to apply.
A Pharmaceutical Company is seeking a Quality Analyst, MicroBiology in Boston, MA.
Role Description • Familiar with aseptic technique • Perform Environmental Monitoring and utilities monitoring. • Perform bioburden, sterility, endotoxin and other routine and more advanced testing. Key Responsibilities/Essential Functions • Perform routine QC testing in accordance with SOPs and cGMP guidelines. Minimal supervision. • Perform verification and approval of data to ensure accuracy. • Assist with audit readiness of laboratory area and calibration and maintenance of laboratory equipment. May assist with ordering. • Utilize a range of electronic systems such as LIMS and document/equipment management software. • Author, review and potentially act as the business owner for SOP changes; participate and lead change controls, CAPAs, investigations, and other quality systems. • Resolve routine and advanced problems by utilizing appropriate resources. Provide problem solving skills to lead and/or support investigations. • May write and execute protocols for procedural and instrumentation validations. • Work on special projects as needed. Lead continuous development and improvement efforts. • Represent Quality Control in team meetings and projects. • Train on and maintain extensive knowledge of current regulatory requirements and relevant internal procedures. • Work independently and as a team player with quality and attention to detail. Good communication skills both oral and written. Effectively and efficiently participate in assigned tasks in a quality manner. • Actively promote safety rules and awareness. Report and take initiative to correct safety & environmental hazards. Work with potentially hazardous chemical, radiological and/or biological materials on a daily basis. Demonstrate good safety practices at all times including the appropriate use of protective equipment.
Skills & Requirements • Typically requires 5-8 years with a BS degree in a related scientific discipline (e.g. microbiology) or equivalent combination of education and previous relevant experience in the pharmaceutical industry, related GMP environment, or equivalent. Other Requirements • Routinely scheduled work, and/or overtime work required on evenings, weekends, and/or holidays, including during adverse weather conditions. Some non-routine travel may be required. • Work with (or in proximity to) potentially hazardous chemical, radiological, and or biological materials and must be able to lift/move materials, e.g. 30 lb. portable equipment, 50 lb. lead/shields.
Why Hays?
You will be working with a professional recruiter who has intimate knowledge of the Information Technology industry and market trends . Your Hays recruiter will lead you through a thorough screening process in order to understand your skills, experience, needs, and drivers. You will also get support on resume writing, interview tips, and career planning, so when there's a position you really want, you're fully prepared to get it.
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Hays is an Equal Opportunity Employer.
Drug testing may be required; please contact a recruiter for more information. #1115741
