Quality Assurance Specialist
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| Job Type | Contractor |
| Location | Dublin |
| Area | Dublin |
| Sector | Quality |
| Start Date | |
| Advertiser | Darcy Ainscough-Denton |
| Telephone | +353 1 574 6266 |
| Job Ref | 2542 |
| Job Views | 482 |
- Description
- Quality Assurance Specialist – Team Horizon
We are currently recruiting an ambitious Quality Assurance Specialist to be part of our client’s team who are a global, research-based biopharmaceutical company that combines the focus and passion of leading-edge biotech with the expertise and capability of an established pharmaceutical leader.
Reporting to the Director of Supplier Quality, this position operates within the Supplier Quality team to support the qualification and post-qualification monitoring of GxP Suppliers. The Supplier Quality team operates globally across the client’s organisation and sits within the wider Central Quality Systems and Compliance group. In this role you will be a contributor in supporting the execution of the company’s plans and maintaining the company’s position as a knowledge leader in the biopharma industry.
Why you should apply:
Our client has developed a stand-out culture of innovation, inclusion, and development, and consistently features as a great place to work.
The role is generously compensated and attracts a competitive base salary.
Excellent career progression opportunities.
What you will bedoing:
Support the Global GxP Supplier approval and update processes.
Support the Supplier Change Notification (SCN) process to ensure Supplier changes are reviewed and assigned to the appropriate owners.
Support the Quality Agreement Management process.
Support process performance projects as directed.
Perform all responsibilities in accordance with company policies, procedures, federal regulations, and safety requirements.
What you need to apply:
BA/BSc or equivalent in Biological Sciences, Chemistry, Microbiology or other science.
6-9 years’ experience in Quality with medical device, pharmaceuticals, or biologics experience.
This position requires the individual to understand and follow written SOPs, record all work legibly and in real time; close attention to detail is necessary.
The person in this position will receive supervisory direction on all routine and non-routine activities. Routine activities will be unsupervised as training and competency develops. The person in this position must have good organizational skills.
The position requires the individual to work collaboratively with colleagues, peers and managers.
A good understanding of the concepts and systems applied to cGMP operations.
The person will have experience with Technical Writing and Problem-Solving methods.
