CRISPR Therapeutics
Biotechnology
QualityControlTechnician,Microbiology
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Quality Control Technician, Microbiology at CRISPR Therapeutics. Skills: Microbiology testing, Environmental monitoring, cGMP compliance. Support routine environmental monitoring of air, surface, and gas utilities for manufacturing of in process and final product drug lots. Collect and process environmental monitoring samples of air, surface, personnel gowning, and gas systems samples according to established schedules or as requested”
Industry & Context.
Sense of urgency in solving problems
Ability to walk, bend, and crouch consistently throughout the shift, Ability to lift sampling equipment weight up to twenty pounds, Ability to wear full gown for up to 50-75% of the shift, this may be for up to 6 hours
What They're Looking For.
Must Have
Associate Degree/Certificate with 1-3+ years relevant GMP experience or BS in Biology or related discipline, Ability to walk, bend, and crouch consistently throughout the shift, Ability to lift sampling equipment weight up to twenty pounds, Ability to wear full gown for up to 50-75% of the shift, this may be for up to 6 hours
Nice to Have
BS in Biology or related discipline, with 0-2+ years of relevant GMP experience, Experience with electronic GMP Quality Systems (ex. LIMS Labvantage and ComplianceWire), Experience with collecting environmental monitoring samples, Experience incubating and analyzing environmental monitoring samples
What You'll Do.
Support routine environmental monitoring of air
and gas utilities for manufacturing of in process and final product drug lots
Collect and process environmental monitoring samples of air
and gas systems samples according to established schedules or as requested
Incubate and analyze environmental monitoring and process gas samples while ensuring activities occur in an efficient and cGMP compliant manner
Maintain accurate sampling and testing records and adhere to cGMP/GDP expectations
and cleaning of Environmental Monitoring instrumentation/ equipment
Assist in everyday organization of the laboratory including safety
and ordering of supplies
How You'll Work.
Team & Collaboration
Collaborative – Openness, One Team
Full Job Description
_**Job Description:**_ **Company Overview** Since its inception over a decade ago, CRISPR Therapeutics has transformed from a research-stage company advancing programs in the field of gene editing, to a company with a diverse portfolio of product candidates across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine, cardiovascular and rare diseases. The Nobel Prize-winning CRISPR science has revolutionized biomedical research and represents a powerful, clinically validated approach with the potential to create a new class of potentially transformative medicines. To accelerate and expand its efforts, CRISPR Therapeutics has established strategic partnerships with leading companies including Vertex Pharmaceuticals. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&D operations based in Boston, Massachusetts and San Francisco, California. **Position Summary** The QC Microbiology team is looking for an engaged, self-driven individual interested in performing microbiology testing to support production activities of the cell therapy products located in Framingham, MA. As an QC Environmental Monitoring Technician, you will support routine environmental monitoring of air, surface, and gas utilities for manufacturing of in process and final product drug lots. **Responsibilities** * Collect and process environmental monitoring samples of air, surface, personnel gowning, and gas systems samples according to established schedules or as requested. * Ability to perform repetitive tasks while maintaining a high attention to detail. * Incubate and analyze environmental monitoring and process gas samples while ensuring activities occur in an efficient and cGMP compliant manner. * Participate in executing method validations and/or classified areas qualifications. * Maintain accurate sampling and testing records and adhere to cGMP/GDP expectations. * Review data,
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