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Microbiologist

Department: Quality
Reports to: QC Microbiology Supervisor

This position is responsible for all microbiological testing of production materials under cGMP conditions. The position provides support and training to Manufacturing staff with regards to aseptic technique, aseptic gowning and proper disinfectant techniques. The position completes all assigned tasks per cGMP and USP requirements and in compliance with Anika’s Quality System

- Perform endotoxin, bioburden and sterility testing for raw materials, work in process and finished goods - Perform testing on water used in the manufacturing process according per USP requirements - Complete all required documentation for results on a timely basis - Review environmental monitoring results in classified areas; identify issues and trends and propose corrective action - Maintain established databases and provide reporting on trends and results as required - Assist with validation as required - Maintain supplies for lab operations - Other duties and projects as assigned

The position requires a Bachelors degree in Microbiology and 3 years hands on bench top experience in a manufacturing environment. Experience with GMP, GLP, FDA and ISO requirements is required. Experience with aseptic media fill and environmental monitoring strongly preferred. The ability to meet hard deadlines is required.



How to Apply

Our definition of a qualified applicant is an individual who has submitted a resume for a specific open position and has illustrated they possess the basic qualifications and skills within the position description.

To apply, select the job description and follow the links or send us your resume via e-mail to resume@anikatherapeutics.com.

No third party resumes accepted.