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Keywords: Katalyst Healthcares & Life Sciences, Location: Jersey City, NJ

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Senior Validation Engineer

: Bachelor's degree in a related life sciences or requisite industry training and experience. 5 - 10 years GMP experience... industry best practices (e.g., ISPE) including development and execution of all applicable system life cycle deliverables (e.g...

Posted Date: 29 Jun 2024

Regulatory Affairs Specialist

Responsibilities: Provides administrative support for regulatory affairs manager Provides RA support for change control projects and sustaining activities Conducts regulatory assessments and determines need for re-registration for propo...

Posted Date: 19 Jul 2024

Regulatory Affairs Specialist

Responsibilities Responsible for the coordination and preparation of document packages for regulatory submissions from all areas of the Company. Keeps abreast of regulatory procedures and changes. Coordinates the collection of documents...

Posted Date: 18 Jul 2024