CQV Engineer
- Dublin
- Contract
- Life Sciences
This vacancy has now expired
Ireland is a hive of activity for the Life Sciences industry at present with global players investing heavily in new and existing facilities here. Here, we are currently supporting our client - one of the world’s largest pharmaceutical organisations – with their latest project
With continued organisational growth including ongoing investment across the portfolio and capital projects programme at their Irish Manufacturing facility just South of Dublin, an excellent opportunity has arisen for a Validation Engineer to join the team.
CQV Engineer Responsibilities:
- Prepare, review and approve documentation for cGMP / Validation of the following: - Equipment, Facility, Utility - Manufacturing Process - Cleaning - Computerised Systems and Automation Packages
- Provide input into project phases from design, commissioning and qualification.
- Preparation, review and approval of Validation documentation.
- Document, resolve and assist in the closure of validation deviations initiated during qualification activities.
- Initiate and management of change control records.
- Evaluate quality standard of service providers for cGMP, including Validation requirements
- 5+ years Validation experience in the Pharmaceutical / Biotech Industry (when / where)
- Need to have experience leading CQV activities for small projects, covering URS’s, design package reviews, FAT's, IQ/OQ/PQ’s.
- CQV Experience with ANY pharma / Biotech manufacturing equipment.
- Equipment which needs qualifying includes: facility / utility upgrade work, Tablet OSD manufacturing equipment: granulators, Capsule fillers, mixers etc.
- Any OSD process manufacturing CQV experience is a bonus
The candidate must have the rights to work in the location stated in the job advert.
Please note, Quanta part of QCS Staffing does not sponsor Visa applications.
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I have always received a highly professional & personable service from the team at Quanta. 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
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’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 Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
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