CQV Engineer
Employer undisclosedRole managed by a recruiter
Perform CQV testing and documentation for small equipment in a sterile drug facility.
21 days ago ago
Intermediate (4-7 years), Expert & Leadership (13+ years), Experienced (8-12 years)
Contractor
Dublin, County Dublin, Ireland
Onsite
Role
What you would be doing
equipment testing
cqv documentation
gmp compliance
safety deliverables
project scheduling
quality records
- Responsible for ensuring that all equipment, is tested in compliance with project related standards from a commissioning perspective.
- Development and execution of CQV testing documentation for benchtop, mobile, analytical, PAT, incubators, BSCs, and TCU equipment for the Sterile Drug product facility.( 100%)
- Responsible for ensuring GMP equipment are tested in compliance with good manufacturing practices, company policies and EU & FDA regulations.
- Responsible for meeting key project deliverables for safety, CQV schedule and quality of project related documentation/electronic records for equipment, utilities assigned.
What you bring
cqv testing
automation
project lifecycle
teamwork
safety
quality
- Demonstratable capacity to effectively execute the CQV testing approach for assigned from initiation to completion.
- Demonstrable experience of performing as part of diverse team of CQV professionals/ contractors to deliver on tasks safely, with quality focus, on time and within budget.
- Experience in CQV of Drug Substance/Drug product small equipment with integrated automation.
- CQV project lifecycle experience from design through to C&Q and handover.
Information not given or found
Training + DevelopmentInformation not given or found
Interview process
Information not given or found
Visa SponsorshipInformation not given or found
Security clearanceInformation not given or found
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