Microbiology Technical Specialist

Integrated Resources, Inc

St. Louis, Missouri

JOB DETAILS
JOB TYPE
Full-time
SKILLS
Assays, Business Development, Cell Cultures, Cleanroom, Clinical Research, Code of Federal Regulations, Computer Skills, Current Good Manufacturing Practice (cGMP), Employee Orientation, FDA (Food and Drug Administration), GMP (Good Manufacturing Practices), Identify Issues, Information Technology & Information Systems, Laboratory, Maintain Compliance, Microbiology, Microsoft Excel, Microsoft Word, Project Tracking, Regulatory Requirements, Rehabilitation Nursing, Sales, Technical Leadership, Technical Writing, Time Management, United States Drug Enforcement Agency (DEA)
LOCATION
St. Louis, Missouri
POSTED
1 day ago
Microbiology Technical SpecialistIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionJob Title: Microbiology Technical SpecialistLocation: St. Louis, MO Duration: PermanentJob Role: The ideal candidate will act as a technical expert to provide technical guidance to lab staff, clientele and sales/business development personnel. This role will be for those with prior lab experience and a desire to enhance their career outside of a supervisor position. The candidate will be expected to work independently with limited supervision. Other responsibilities include:Oversight of technical projects including method development, validations, verifications and transfers.Technical writing including, but not limited to, authoring protocol and summary reports.Troubleshooting methods; conducting investigations into non-conformances, deviations, OOS and CAPAs.Ensuring compliance with CFR, FDA, DEA, and GMP regulatory requirements.Qualifications: BS/MS degree in Microbiology or related scientific discipline with 5+ years of experience in a cGMP regulated environment. Extensive knowledge of Microbiology principles with extensive experience in 3 or more of the following areas: Technical Writing, Sterility (Clean room or isolator), Bacterial Endotoxin Testing, Microbial Limit Testing, Antibiotic Assays, Antimicrobial Effectiveness Testing, Cell Culture. Experience meeting aggressive timelines. Strong computer experience using professional tools such as Excel and Word.Additional InformationWe do have referral bonus of $500 per candidate, if you refer any of your friends or colleague who are looking out for the same job.

About the Company

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Integrated Resources, Inc