
C&Q Engineers
1 week ago
Overview
C&Q Engineer - Ireland, Dublin - 12 Months Contract.
With more than 2,000 employees, more than 300 million units per year, and a pipeline of innovative medicines, our client is one of the largest production units in the world.
The company produces, packs and distributes in a high-tech environment, sterile injectable medicines.
More than 1 million injectable medicines are produced, packaged and distributed every day to 170 countries worldwide.
This role supports delivery of a new state-of-the-art facility on an initial 12-month contract.
Responsibilities
Participate in design document reviews and ensure quality aspects are included in design.
Attend FAT and execution of agreed testing protocols and sign off on permission to ship forms.
Generate CQV documents at project level and for specific equipment/systems.
Liaise with Quality, Engineering and CQV to align on Critical parameters and document content.
Track and confirm closure of action items identified through FAT, HAZOP, Design Qualification and other reviews.
Maintain a strong interface with the Automation and Engineering teams to ensure information flow meets project needs, resolving issues as they arise.
Participate in construction system completion walkdowns.
Perform shakedown, commissioning and qualification of systems.
Desirable Experience / Qualifications
B.Sc/B.Eng.
degree in engineering discipline, with emphasis on mechanical or process engineering.
Extensive experience in biotechnology or pharmaceutical GMP manufacturing/CQV environment.
Ability to work on own initiative and proactively respond to business needs.
Excellent interpersonal and communication skills.
Familiarity with Delta-V & Navis Works is an advantage.
Additional Details
Seniority level: Entry level
Employment type: Contract
Job function: Engineering and Information Technology
If this role is of interest to you, please apply now
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