Categories: Careers
      Date: Mar 25, 2010
     Title: Quality Control Supervisor

The Quality Control Supervisor will be responsible for supervising the Quality Control Microbiology/Environmental Monitoring Laboratory and the Quality Control Analytical Laboratory.

Responsibilities:

• Provide technical expertise with microbiological and chemical test procedures, methods, and equipment within the QC Laboratory of a Biopharmaceutical, GMP Manufacturing Facility.
• Direct QC testing on final products, product intermediates, raw materials, water, and environmental samples to assure conformance to specification, action or alert limits; confirm safety of material, equipment and process environment for continued production. 
• Organize testing associated with product and cleaning validations and equipment qualifications.
• Evaluate methods and equipment for effectiveness.

Qualifications:

• Four year scientific degree with five + years of relevant experience working within a Quality Control Lab of a FDA regulated business, preferably pharmaceutical production.
• Experienced with laboratory instruments, procedures and test methods: HPLC, TOC, ELISA, LAL, electrophoresis, particulate content, material identification, host-cell DNA or protein, bioburden, sterility, mycoplasma, viral contamination, environmental monitoring, etc.
• Knowledgeable in OOS investigations, GLPs and GMPs.
• Ability to read and interpret technical procedures, FDA Guidelines and professional journals.
• Strong written and oral communication skills, detail-oriented and ability to work within multifunctional teams, and ability to prioritize work.

To apply for this position, please submit your resume including the position you are applying for to careers@cytovance.com or send it via postal service to Human Resources, 840 Research Parkway, Suite 400, Oklahoma City, OK 73104.