QA Specialist – GMP Compliance
The Specialist is a member of a team within Quality and is involved in supporting the GMP Quality Assurance activities at the site. This is an 11 month contract.
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The Specialist is a member of a team within Quality and is involved in supporting the GMP Quality Assurance activities at the site. This is an 11 month contract.
This is for the position of Process Engineer for a pharmaceutical company based in Carlow. This is a hybrid role (2-3 days on site minimum). It is an 11 month contract, with salary based on relevant experience.
Responsible for supporting the Engineering Department in a GMP and Sterile Environment. Ensure that objectives are effectively achieved, consistent with requirements to ensure compliance, safety and reliable supply to our customers.
Responsible for ensuring that the process for the manufacture of drug product at the Carlow site is in compliance with cGMP and the associated regulatory requirements. Responsible for reviewing and approving GMP documentation to support corporate compliance/regulatory expectations for manufacturing operations. Ensure that objectives are effectively achieved, consistent with requirements to ensure compliance, safety and reliable supply to our customers.
Opportunity to enter or expand your experience in the biopharma sector with this quality technician position. 11 month contract on site in Carlow.
Critical to have an understanding of Upstream and Downstream Unit Operations for mAb manufacturing and must have understanding of both continuous and batch fed manufacturing processes. A level 6 with a minimum of 3+ years' experience in a GMP Manufacturing requirement shall be deemed equivalent
This is data manager role with a large pharmaceutical company based in Dublin. The position is Monday to Friday. 11 month contract. The salary is up to 100k depending on experience. As a Data Manager, you will be vital in building our animal data models, working closely with Marketing, IT, and R&D leads and teams to explore the data our products upload to our data platform.
Responsible for supporting the Quality Control Department in the management of external sample shipments and retain sample management. Support various administrative duties associated with sample management. Ensuring that objectives are effectively achieved to, consistent with requirements to ensure Compliance, safety and reliable supply to our customers. This is a Day role based on site (Mon-Fri).
Operate and/or monitor production activities and support equipment, using MES/DCS and PLC based systems, to ensure optimum equipment uptime and target outputs. Equipment will include, yet is not limited to, parts washers, autoclaves, portable tank CIP/SIP/storage panels, Vial Washer, Depyro Tunnel, Debagger and filling machines
This is an amazing opportunity for a Quality Assurance Specialist to join our quality team. You will play a vital role in supporting the introduction of new products and Quality oversite of executed validation completed at our Carlow facility. As the QA Specialist for Validation and New Product Introduction (NPI), you will be an essential member of our esteemed Technical Transfer/Validation Team. This team holds responsibility for managing the development and manufacture of vaccines and biologic