Why Mayo Clinic
Mayo Clinic is the nation\'s best hospital (U.S. News & World Report, 2022-2023) and ranked #1 in more specialties than any other care provider. We have a vast array of opportunities ranging from Nursing, Clinical, to Finance, IT, Administrative, Research and Support Services to name a few. Across all locations, you\xe2\x80\x99ll find career opportunities that support diversity, equity and inclusion. At Mayo Clinic, we invest in you with opportunities for growth and development and our benefits and compensation package are highly competitive. We invite you to be a part of our team where you\xe2\x80\x99ll discover a culture of teamwork, professionalism, mutual respect, and most importantly, a life-changing career!
Mayo Clinic offers a variety of employee benefits. For additional information please visit . Eligibility may vary.
Position description
Participates in selection, purchase, validation, and implementation of GMP grade equipment and supplies. Responsible for upkeep and maintenance of GMP grade equipment in the cleanroom suite. Is knowledgeable in FDA and other regulatory requirements and maintains the manufacturing facility in accordance to regulatory requirements. Writes Standard Operating procedures as it relates to GMP grade equipment and use of the cleanrooms for manufacturing. Assists QA department in getting the GMP facility ready for regular audits and inspections. Conducts routine environmental monitoring tasks as defined by the laboratory director. Responsible for the training and competency assessment of all manufacturing techs and/or environmental monitoring techs, who enter and use the GMP facility. Provides technical direction and assistance for questions and problems that arise in the GMP area of the laboratory on a day to day basis.
Qualifications
Bachelor\'s degree in clinical laboratory science (CLS), or medical technology (MT), chemistry, or a human biological science; AND, minimum of four (4) years of relevant laboratory experience in Human Cellular Therapy. Experience in working in GMP facility is required. Knowledge of regulatory standards and requirements such as GMP, GTP, cleanroom requirements, environmental monitoring, FACT and AABB is required. Must have proven experience with validation, implementation, operation, and troubleshooting of laboratory instruments and assays. Good organizational, communication, problem solving, and computer skills.
**This position is not eligible for visa sponsorship. Also, Mayo Clinic DOES NOT participate in the F-1 STEM OPT extension program**
Additional qualifications
Capable of performing under time constraints, multitasking, and working in a fast-paced and changing environment. Demonstrate good communication skills and be able to work closely with others. Able to work independently. Ongoing willingness to upgrade job skills.
Requires CV/Resume, unofficial transcript(s), and for foreign trained lab personnel to provide a detailed equivalency evaluation to include US equivalent degree at the applicants expense.
For international/foreign trained applicants, it is the responsibility of the international/foreign to provide to Mayo Clinic the following information. The applicant is responsible for the cost associated with obtaining the equivalency evaluation.
International transcript:
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