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Supervisor, Microbiology

Covidien

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Job Snapshot
Location:
3600 North Second Street
Saint Louis, MO 63147 (map it!Map it! )
Base Pay:
$60,076 - $81,103 /Year
Other Pay:
RFR Bonus Plan
Employee Type:
Full-Time
Industry:
Pharmaceutical
Manufacturing
Manages Others:
Yes
Job Type:
Pharmaceutical
Manufacturing
Education:
4 Year Degree
Experience:
At least 5 year(s)
Travel:
None
Relocation Covered:
Yes
Post Date:
11/5/2009
Contact Information
Contact:
Veta Gray
Description Supervise a Quality Team to ensure that plant operations meet all regulatory compliance requirements.  This position will manage quality activities including environmental monitoring and microbiology.
  • Directly supervise staff for Manage team member assignments to ensure tasks are completed accurately and on schedule.
  • Staffing responsibilities include hiring, training, and managing employee accountability and development. 
  • Coordinate activities among production, laboratories, engineering, and others to ensure testing/product release schedule is met. 
  • Must be willing to  perform Microbiology testing as necessary.
  • Review and approve change control, validation protocols (IQ, OQ, PQ, PV) and reports, Standard Operating Procedures, Standard Test Methods, Specifications, investigations, Batch Records, CAPAs, and exception reports. 
  • Trending of environmental and microbial data. 
  • Provide periodic review and update of controlled documents.
Requirements Education required/ preferred: Bachelor’s degree in microbiology or related field is required. 

Experience:
  • Two or more years of supervisory experience and five or more years of QC experience in a FDA regulated environment preferred.
  • Experience supervising personnel on multiple shifts is preferred. 
  • Experience in a pharmaceutical manufacturing environment.

 

Preferred Skills/Qualifications:
  • Expertise in the manufacture and control of sterile products, microbiological analysis techniques and statistical quality control. 
  • Good working knowledge of FDA aseptic processing requirements and USP/EP/ISO guidelines. 

  • Background should include analytical method validation work. 

  • Ability to use relevant software packages to process and analyze data.

     

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