Website Karwell Technologies
Karwell Technologies
Company : Karwell Technologies
Job Description:
The Validation Resource for Utilities and Facilities is responsible for ensuring the qualification and validation of critical utility systems and facility infrastructure in a GMP-regulated environment. This includes HVAC systems, water systems (e.g., WFI, RO/DI), cleanrooms, compressed gases, and other support utilities. This resource have to ensure compliance with industry standards and regulatory requirements while working closely with cross-functional teams to support new installations, system upgrades, and operational readiness.
Roles & Responsibilities:
Commissioning Activities
" Plan and execute commissioning activities for utility systems (e.g., HVAC, purified water systems, clean steam, compressed gases) and facilities (e.g., cleanrooms, environmental monitoring systems).
" Troubleshoot and resolve technical issues during the commissioning phase.
Qualification & Validation
" Author, execute, and review qualification protocols (IQ, OQ, PQ) for utilities and facilities.
" Validate critical systems, including HVAC balancing, environmental monitoring, water quality testing, and cleanroom certification.
" Ensure systems meet performance requirements and GMP standards.
" Perform thermal mapping, pressure testing, and other critical tests as needed.
Documentation
" Develop and maintain accurate and complete documentation, including protocols, validation reports, and SOPs.
" Document deviations, CAPAs, and change controls associated with facilities and utilities systems.
" Ensure traceability of qualification activities in alignment with the Validation Master Plan (VMP).
Compliance and Risk Management
" Ensure all utility and facility qualification activities meet global regulatory requirements (e.g., FDA, EMA, WHO).
" Perform risk assessments and develop mitigation strategies for utility and facility systems.
" Ensure compliance with 21 CFR Part 11, Annex 11, and applicable ISO standards.
- Requirements:
- 3 5 years of experience in commissioning, qualification, and validation of utilities and facilities in a pharmaceutical, biotech, or regulated manufacturing environment.
- Hands-on experience with systems such as HVAC, purified water, clean steam, gases, and cleanrooms.
- Kneat experience.
- Familiarity with environmental monitoring and building management systems (Client).
- Manufacturing plant and utility environments, including cleanrooms.
- Flexibility to work extended hours or weekends during critical project phases.