Position: Quality Analyst Duration: 6 - 12 Months Location: Rochester NY REQ ID # 3828 Responsibilities: Candidate will initially learn the LIMS Software System and be responsible for Test Designing, Fluid Preparation, Slide Labelling and other lab duties in the SPQC Lab. Candidate must be willing to learn to run, maintain and troubleshoot Vitros 350, XT3400, FS 5, 1, and 4600 analyzers. As an FDA regulated facility, documentation is key to this position in order to meet regulatory requirements; therefore, candidate must have an understanding of cGMPs and documentation in a regulated industry. Full understanding of quality control is expected. This position requires an individual who can multi-task, adapt to changes in daily workload and priorities, and function in a cross-functional team setting. Maintains a clean and orderly work area in lab and office. Uses Quality Systems for document retrieval and on-line learning. Identifies unacceptable product quality and takes appropriate actions. Some lifting not to exceed 50lbs. Manual dexterity of handling instruments and repetitive motion. Standing for long periods of time. Wears appropriate PPE in the lab. Participates in Overtime as required by the organization. Qualifications: A BA/BS Degree or equivalent is required. A Degree in science concentration is preferred. Year experience is required. Experience in documentation protocols and procedures are a plus Candidate must have a demonstrated proven track record of planning and organization of daily workload, high affinity toward teamwork and demonstrated problem solving using innovative solutions. Careful attention to detail and accuracy of work are required. Having a working knowledge of computers and windows software is desired.
