Responsibilities: Microbiological testing for release of product by microbial enumeration per USP <61>, bioburden, bacterial endotoxin and particulate testing. Other responsibilities are testing of raw materials and in-process samples, enumeration and interpretation of environmental isolates, and other GMP governed procedures including but not limited to environmental monitoring, water bioburden and bacterial endotoxin testing and media growth promotion. The QC Microbiologist may be required to prepare status and microbiology reports, perform method validation and transfer, and author/revise procedures and SOPs as needed. The QC Microbiologist is responsible for complying with current Good Manufacturing Practices.
Requires: BS preferably Microbiology or a Science degree; Experience in a pharmaceutical manufacturing facility is highly preferred, experience in a FDA regulated/cGMP environment is highly preferred; One to three years of prior laboratory experience/knowledge; Excellent written/verbal communication skills; Ability to provide leadership, teamwork, and cooperation; Good computer skills.
This position will require working approximately 4 hours per month on Saturday/Sunday.
Location: Cambridge
Compensation: $20-$25/hr.
This is a contract job.
Principals only. Recruiters, please dont contact this job poster.
Please, no phone calls about this job!
Please do not contact job poster about other services, products or commercial interests.
