Katalyst Healthcares and Life Sciences
Job Location :
Framingham,MA, USA
Posted on :
2025-01-01T07:06:10Z
Job Description :
Responsibilities:
- Writes and executes commissioning, qualification, & validation protocols for facilities utilities, equipment, and computerized systems.
- Resolves protocol discrepancies and deviations.
- Reviews vendor generated validation protocol packages.
- Responsible for the generation of complex protocols using a risk-based approach that meets current regulatory requirements and industry practices.
- Excellent oral and written communication.
- Ability to effectively manage time and prioritize tasks independently.
- Excellent organizational skills.
- Ability to manage day-to-day operations in a fast-paced environment.
- Ability to effectively manage several tasks simultaneously.
- Must be self-motivated and have a proven ability to work in a team environment.
- Min Education Bachelor's degree.
- plant utilities, clean utilities, CIP, SIP, Fill Finish, HVAC, Filling lines, CTUs .
Requirements:
- Validation experience specific to pharma or biotech - 7+ years of experience.
- Knowledge in data acquisition systems, such as Kaye.
- plant utilities, clean utilities, CIP, SIP, Fill Finish, HVAC, Filling lines, CTUs, component prep equipment, formulation.
- Well-developed communication skills, both verbal and written.
- BSc/BEng plus previous experience in CQV field or equivalent combination of education and experience.
- Experience in pharmaceutical/biopharmaceutical industry or related industry/manufacturing environment.
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