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Location
Framingham, MA, United States
Compensation
Not disclosed
Level
director
Type
full time · On-site

Posted by employer 2 days ago

First seen on Joblaze 4 hours ago

Last verified on the company career page 4 hours ago

Not disclosed in this posting: compensation, years of experience, visa sponsorship.

Joblaze summary

The Quality Site Head at CRISPR Therapeutics oversees the quality assurance and compliance processes within the facility, ensuring that all operations meet regulatory standards. This role requires expertise in quality management systems, regulatory affairs, and a strong background in biotechnology or pharmaceuticals. It is suited for a senior professional with extensive experience in quality control and assurance, ideally in a manufacturing environment. The position plays a critical role in maintaining the integrity of the company's innovative therapeutic developments.

Joblaze insights

  • Listed today — first seen on Joblaze October 1, 2026. Last confirmed on CRISPR Therapeutics's careers page October 1, 2026.

Quick facts

Is the Quality Site Head role remote?
No — this is an on-site role in Framingham, MA, United States.
Where is the role based?
CRISPR Therapeutics is hiring for this position in Framingham, MA, United States.
What seniority level is this role?
CRISPR Therapeutics targets director candidates for this position.
Is this full-time or contract?
Full-time for this Quality Site Head role at CRISPR Therapeutics.

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