This job has expired

Senior Microbiologist

Gulfport, Mississippi, US
Closing date
Dec 12, 2022

View more

Consultancy/Private Sector
Conservation science
Salary Type
Employment Type
Full time
You need to sign in or create an account to save a job.
Kelly Services is actively recruiting for a Sr. Microbiologist for a pharmaceutical manufacturing company. This is a perm (Direct Hire) opportunity!

Location: Gulfport, MS (100% onsite is required.)
Work Schedule: M-F, flexible start (4am up to 11am).
Salary: Dependent on experience. Probably an exempt position.
If non-local, relocation assistance may be provided.
Must be able to provide proper documentation that proves ability to work in the U.S.

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.

Candidate must have extensive FDA/GMP related microbiology industry experience to be considered.

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).
* 10+ years of microbiology experience required. (FDA/GMP industry experience.)
* 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.

Candidates are encouraged to apply for immediate consideration. Hiring Manager is looking to fill this opportunity as soon as possible.
You need to sign in or create an account to save a job.

Get job alerts

Create a job alert and receive personalized job recommendations straight to your inbox.

Create alert