Senior Raw materials Analyst
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| Job Type | Contractor |
| Area | Dublin, Ireland |
| Sector | Laboratory/Scientific |
| Start Date | |
| Advertiser | Mary King |
| Job Ref | 1002877 |
| Job Views | 1180 |
- Description
- Team Horizon is seeking a Senior QC Analyst for our client based in Dublin. As a part of this role you will be point of contact for raw material testing (within QC and contract Laboratory). You will also coordinate and document sample shipment to Contract Laboratory facility.
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.
Our client has developed a stand-out culture of innovation, inclusion, and development, and consistently features as a great place to work.
What you will be doing:
Monitor contract laboratory sample turnaround time.
Coordinate and document result retrieval from Contract Laboratory facility.
Review and Verify QC data.
Generate Material Specification Reports and associated documentation.
Generate CoA’s for raw materials.
Investigate and determine Root Cause associated with laboratory deviations and investigations.
Compile trend analysis and write associated reports for internal and regulatory.
Manage, communicate and document compendia updates as required.
Author/revise and contribute to test methods; SOPs; Material Specification Reports; protocols, technical studies and/or reports.
Generate SOP’s/other documentation as applicable.
Performing all task as per GMP requirements.
Assist in additional duties as directed by the QC Lab Support supervisor.
Supports CAPA and change control through participation in project planning and collaboration.
And other duties required
What you need to apply:
Degree in chemistry or biological science with a preference for Analytical Chemistry or Biochemistry
Degree qualification in relevant science discipline.
Preferably 3 years post educational experience with experience working in a regulated GMP environment preferably within a Pharma/Biotech facility.
Planning/scheduling of own work and that of a team
An ability to work independently, as well as a member of a team in a dynamic, fast-paced environment.
Excellent written and oral communication skills.
Understand GMP requirements.
