Quality Control Microbiology Specialist

Requirements

• B.S./M.S. in Life Sciences or related field with 0-3 years of experience, in GMP QC Laboratory.
• Proficient in microbiology methods (plate enumeration, growth promotion, microbial ID, etc.) and aseptic technique needed to perform EM in a GMP environment.
• Strong knowledge of US and EU cGMP regulations/guidance.
• The ability to work and lead in a fast-paced environment, manage priorities, and maintain timelines for multiple projects is essential.
• Effective communication skills, both verbal and written, at all levels and across various functions.

Additional Information

About eGenesis eGenesis is a clinical-stage biotechnology company developing human-compatible engineered organs to address the severe global organ shortage. The Company's proprietary genome engineering platform enables extensive, multiplex gene edits to remove key biological barriers, add protective human transgenes, and inactivate endogenous retroviruses. EGEN-2784, a genetically engineered porcine kidney, is the Company's lead program and is currently being evaluated in a multi-patient Expanded Access study at MGH. eGenesis is headquartered in Cambridge, MA. POSITION SUMMARY eGenesis is seeking an innovative QC Microbiology Specialist to lead and provide the technical and strategic oversight of eGenesis' environmental monitoring program. In this position you will be responsible for hands on environmental monitoring sampling, testing, reporting and trending of eGenesis' two GMP manufacturing facilities (Greater Madison Area and Northwest Indiana). You will ensure activities are executed in a cGMP compliant manner and will work collaboratively on implementation and maintenance of our contamination control program. The ideal candidate will be independently motivated, a strong communicator and demonstrate proficiency in regulatory compliance. This position will be an onsite position in the Greater Madison Area.

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