Microbiology Lab Supervisor

Industry

Pharmaceuticals

Advert ID

USA/414716

Location

Newberry,Columbia - Lexington County,Augusta,Aiken

Job Type

Permanent

Hours

Full-Time

Salary Range

68000.0 - 70000.0 YEARLY

No. of Openings

1

Branch Information

Aiken, SC - (USA) 152 Rudy Mason Parkway, NE SC Aiken , SC - 29801 Phone : 803-642-0750

ContactNumber

803-642-0750

Job Description

Manpower has an opening for a Microbiology Lab Supervisor in Aiken, SC. The usual working hours are Mon-Fri 8AM to 5PM, although this job will also require a flexible schedule. Salary will be based off of experience. Job duties would include but not be limited to:
• Supervise Microbiology Laboratory
• Oversee and conduct USP and EP microbiological analyses of raw materials, finished products, and environmental monitoring samples to include:
• OOS/Atypical results investigations.
• Troubleshooting Microbiological Methods application.
• Troubleshooting laboratory instrumentation.
• Write and execute laboratory equipment qualification protocols (e.g., refrigerators, water baths, incubators, autoclaves, etc.).
• Review raw data, testing frequency, quality control specifications, and pharmacopoeia procedural revisions for correctness, compliance, and accuracy.
• Support Regulatory Inspections and Audits (i.e. FDA, EMA, MRHA, CAG, etc.)

Required:
• Bachelor of Science Degree in biology
• Microbiology degree preferred
• Minimum of 7 years’ experience in Microbiology Laboratory
• Experience serving as a subject matter expert in microbiology during regulatory inspections and audits
• Working knowledge of particle counters, air sampling equipment, laboratory bio-safety, Quality Management standards, and GMP requirements.
•Knowledge and work experience in a FDA regulated manufacturing and/or packaging facility is preferred.

Required:
• Bachelor of Science Degree in biology
• Microbiology degree preferred
• Minimum of 7 years’ experience in Microbiology Laboratory
• Experience serving as a subject matter expert in microbiology during regulatory inspections and audits
• Working knowledge of particle counters, air sampling equipment, laboratory bio-safety, Quality Management standards, and GMP requirements.
•Knowledge and work experience in a FDA regulated manufacturing and/or packaging facility is preferred.