Quality Control Micro Analyst II
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| Job Type | Fixed Term |
| Area | Dublin |
| Sector | Laboratory/Scientific |
| Start Date | |
| Advertiser | Mary King |
| Job Ref | 2593 |
| Job Views | 429 |
- Description
- Team Horizon is seeking a Quality Control Micro Analyst II for our client based in Dublin on a 12-month contract.Our client 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.
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 be doing:
Provide technical support with regard to method verification, Environmental Monitoring, Utilities and all other lab-based activities.
Support validation/verification and qualification of test methods and processes.
Troubleshoot laboratory methods and instrument issues as they arise.
Completion of project work and implementation of initiatives designed to improve the efficiency of the laboratory function/department.
Investigate out of specification/limit results utilizing Structured Problem Solving, Root Cause Analysis tools in conjunction with the QC Manager, QA and other relevant departments and to implement effective corrective and preventative actions.
Lead and participate in Quality Risk Assessments relating to QC.
Technical report writing in support of routine testing and method verifications.
Perform technical review of data generated in laboratory, validation protocols and reports.
Represent the QC department in internal and external audits where appropriate.
What you need to apply:
Degree in Science/ Microbiology or related science.
Minimum of 5 years of experience in cGMP Quality environment.
Experience in testing of sterile drug product and aseptic filling process of sterile pharmaceutical /biopharmaceutical products.
Good knowledge of current regulatory requirements for QC / Sterility Assurance in support of cGMP operations supporting clinical and commercial manufacturing.
Experience in Quality Risk Management.
Excellent knowledge of LIMS.
