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  1. Investigative Writer – GMP SOP Pharmaceutical

    Full Time Permanent Position for a large US Company. B-851 Investigative Writer – GMP SOP Pharmaceutical Location: Job is in Buffalo, NY Domain:  Manufacturing Experience: 3-20 Years   Experienced Investigative Writer   is required having responsibility for Ensuring compliance with relevant SOPs, while gathering, analyzing and applying information from internal and external sources to perform a risk assessment;   Job Responsibilities: Investigating process deviations and customer ...

  2. Sr. Quality Engineer, Critical Systems

    Developing, evaluating and ownership of all quality characteristics of the plant facilities and equipment quality system (critical systems); Reviewing and approving all non-routine validation, re-qualification and change control documents from a compliance perspective; Working in partnership other departments to solve problems and provide expertise on compliance issues; Approving validation, engineering, laboratory, computerized system documents to ensure accuracy, cGMP compliance, ISO, etc.; ...

  3. Microbiologist

    Job title: Microbiology Medical Technologist - FT 75hrs Per Pay Period Posted on: 04/16/2014 Status: Full Time Job Description Performs, interprets and evaluates routine and complex diagnostic procedures applying the principles, theories and techniques of clinical laboratory sciences. Participates in continuous quality improvement activities and educational experiences in support of departmental philosophy and objectives, as well as, initiatives. B.S. Medical Technology or Related Science or ...