CRISPR Therapeutics

Biotechnology

QualityControlTechnician,Microbiology

$0–0k Framingham, Massachusetts, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“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.

Biotechnology
Problems you'll solve

Sense of urgency in solving problems

Eligibility Requirements

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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