The Role
The Senior Quality Microbiologist conducts microbiological assays for pharmaceutical quality control, prepares samples, documents results, calibrates instruments, and ensures compliance with CGMP regulations.
Summary Generated by Built In
Allen Spolden is actively recruiting for a Sr. Microbiologist with pharmaceutical manufacturing experience. This is a perm (Direct Hire) opportunity.
Relocation assistance will be provided
Location: Gulfport, MS (100% onsite is required.)
Work Schedule: M-F, flexible start (4am up to 11am).
Salary: Dependent on experience. Probably exempt position.
The Sr. Microbiologist will provide quality control support to pharmaceutical manufacturing operations by conducting various microbiological assays for the purpose of microbial growth detection and identification.
Principal Duties include:
- Perform routine preparation of samples and reagents used for testing analysis.
- Report and document results following established procedures.
- Prepare liquid and solid media.
- Participate in laboratory investigations of out of trend/specification results.
- Calibrate, operate, and maintain analytical instrumentation for product testing, including routine preventive maintenance and troubleshooting.
- Actively contribute to a team setting within the laboratory and potentially with other work teams to increase efficiency, solve problems, generate cost savings, improve quality, and provide new product support.
- Ensure personal training requirements are met and that training records are current.
Knowledge and Skill Requirements:
- Minimum of a BS in Biology or Microbiology (or related discipline).
- 4-5 years of microbiology experience required.
- Proficiency in microbiological techniques such as aseptic testing, microbial monitoring, gram staining, and plating.
- Knowledge and control of analytical equipment including calibration and maintenance.
- Knowledge of computer software, including relevant applications such as Microsoft Office.
- Knowledge of CGMPs regulations.
- Understanding of quality systems including change control, deviations and CAPAs.
- Ability to handle multiple tasks concurrently and complete tasks in a timely manner.
- Strong written and verbal language skills to effectively read and write SOP’s and related lab reports and communicate with personnel at all levels in the organization.
Requirements
Education and Experience
- · B.S. in Biology or equivalent experience.
- · 4-5 years’ experience in Microbiology
- · Pharmaceutical Manufacturing Laboratory experience required.
- · Knowledge of computer software, including relevant applications such as Microsoft Office.
- · Expert knowledge and understanding of quality control, SOPs, cGMPs, OSHA, and FDA policies and regulations.
Benefits
Benefits:
- Dental insurance
- Health insurance
- Life insurance
- Paid time off
- Vision insurance
Skills Required
- B.S. in Biology or Microbiology
- 4-5 years microbiology experience
- Pharmaceutical Manufacturing Laboratory experience
- Knowledge of Microsoft Office
- Expert knowledge of quality control and cGMPs
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The Company
What We Do
Allen Spolden specializes in clinical research operations management and provides tailored workforce solutions for clinical research organizations, pharmaceutical, biotech, and healthcare sectors. They offer services in clinical research, data management, regulatory affairs, and talent acquisition.
