C&Q Engineer
- Ireland, Dublin
- Contract
- Compliance / Quality Assurance
With more than 2,000 employees, more than 300 million units per year, and a lot of innovative medicines in the pipeline, no wonder our client is one of the largest production units in the world! Our client 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. Their destination: 170 countries, worldwide!
Do you want to work with an exciting company who are an established market leader within their niche field? We have a fantastic opportunity for a C&Q Engineer to work on an exciting CapEx project in Dublin on an initial 12 month contract. As a C&Q Engineer you will play a key role in the successful delivery of a new state of the art facility.
Essential Duties and Responsibilities for this C&Q Engineer role include, but are not limited to, the following:
- Participate in design document reviews and ensure that 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. Liaising with Quality, Engineering and CQV to align on Critical parameters and document content.
- Track and confirm closure of actions items identified through FAT, HAZOP, Design Qualification and other reviews.
- Maintain a strong interface with the Automation and Engineering teams to ensure that the information flow meets the needs of the Automation and Engineering teams, resolving issues as they arise.
- Participate in construction system completion walkdowns.
- Perform shakedown and commissioning and qualification of systems.
- B.Sc/B.Eng. degree in engineering discipline, with particular emphasis mechanical or process engineering.
- Extensive experience from biotechnology or pharmaceutical GMP manufacturing/CQV environment.
- Demonstrated ability to work on own initiative and proactively respond to business needs.
- Excellent interpersonal and communication skills.
- Familiar with Delta-V & Navis Works an advantage
- Extensive Clean in Place (CIP) experience
#LI-BP1
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing's speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
I have always received a highly professional & personable service from the team at QCS Staffing. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
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