This key position will oversee the quality control support of multiple
technologies. You will facilitate the performance, qualification,
validation, and transfer of new or current QC procedures. You will be
responsible for the day to day activities of numerous QC laboratory
operations in support of production, validation, and development activities.
The ideal candidate will have a BS or MS in Microbiology, Chemistry, Medical
Technology, or a closely related discipline with a minimum of 7 years of
related work experience with 3 years of lead analyst or supervisory
experience. A thorough knowledge of cGMP regulations and regulatory
inspection requirements is required. A demonstrated experience and knowledge
in managing multiple laboratories and/or operations.
Please contact Eric at scientificresources.com for more information or to
submit your resume