Associate Quality Control
| Job Type | Contractor |
| Area | Dublin, Ireland |
| Sector | Laboratory/Scientific |
| Start Date | |
| Advertiser | Mary King |
| Job Ref | 1003597 |
| Job Views | 81 |
- Description
Team Horizon is seeking a Associate Quality Control for our client based in South Dublin. The role undertakes implementing continuous improvement projects and supporting a lean culture and Right First Time (RFT). The role also represents the QC unit by liaising with internal and external customers.
Additionally, the role may involve carrying out additional work functions that are not described in this specification but are associated with their role.
Why you should apply:
- This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
- There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
- Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.
What you will be doing:
- Under minimal supervision, responsible for one or more of the following activities in QC including: Reagent management, media preparation, GMP document review and management, sample and data management and some analytical testing.
- With a high degree of technical flexibility, work across diverse areas within the lab
- Plan and perform routine tasks with efficiency and accuracy.
- Review, evaluate, back-up/archive, and approve analytical data.
- Troubleshoot, solve problems and communicate with stakeholders.
- Participate in audits, initiatives, and projects that may be departmental or organizational in scope.
- Evaluate lab practices for compliance and operational excellence improvement on a continuous basis.
- Approve lab results
- May participate in lab investigations.
- May provide technical guidance.
- May train others.
- May contribute to regulatory filings.
- May represent the department/organization on various teams
- May interact with outside resources.
What you need to apply:
- Bachelor’s degree in a science discipline.
- 1-2 years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry.
- Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.
