QC Associate Microbiology Specialist

QC Associate Microbiology Specialist.We are actively recruiting for a QC Microbiology Specialist to provide technical support to the QC Microbiology Lab & operations to ensure the continued manufacture and supply of quality pharmaceutical products within a leading Pharmaceutical Manufacturing multinational.Key Responsibilities: * Development and execution...

LSC have a great contract opportunity for a QC Associate Microbiology Specialist to join a global Biopharmaceutical company in Carlow. This is a state-of-the-art vaccines and biologics manufacturing facility currently producing many products in various therapeutic areas including: oncology, autoimmunity, pneumonia, and infectious disease. If you have 5+...

Purpose As QC Bioassay Analyst you will perform and review a range of techniques such as immunoassays, cell based potency bioassays and asceptic techiniques as part of routine and non-routine testing and project work to ensure processes and end products comply with corporate and regulatory requirements to facilitate product release. Reporting to the Bioassay...

This is an 11-month contract and is a 2-shift cycle. This is an onsite role. Purpose Responsible for ensuring that the process for the manufacture of drug products at our Carlow site complies with cGMP and the associated regulatory requirements. Responsible for reviewing and approving GMP documentation to support corporate compliance/regulatory expectations...

Quality Assurance Specialist – Validation and NPIAn amazing opportunity has arisen for a Quality Assurance Specialist to join the quality team within a leading Biopharmaceutical Multinational. As a member of the Tech Transfer/Validation Team you will play a vital role in supporting the introduction of new products and Quality oversite of executed...

QA Validation Specialist (New Product Introduction) 11 month contract On site Carlow AMC22404 I am on the lookout for a QA Specialist for Validation and NPI for a rapidly expanding biotechnology manufacturer in Carlow. You will be an essential member of the Technical transfer and Validation team responsible for managing development and manufacturer of...

LSC have a great contract opportunity for a QA Specialist to join a global Biopharmaceutical company in Carlow. This is a state-of-the-art vaccines and biologics manufacturing facility currently producing many products in various therapeutic areas including: oncology, autoimmunity, pneumonia, and infectious disease. If you have 3 years of experience working...

This is an 11-month initial contract. Purpose In this role, 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...

The role: PE Global is currently recruiting for a QA Validation Specialist on behalf of a leading pharmaceutical company based in Carlow. This is an initial 11-month contract role. Description: Carlow is offering an amazing opportunity for a Quality Assurance Specialist to join our quality team. In this role, you will play a vital role in supporting the...

QA Associate Specialist - Shift RK22685 Contract 11 months On site - Carlow Were currently recruiting for an exciting opportunity with a multinational Pharmaceutical organization based in Carlow. This is an excellent position for anyone who is looking to join a leading multinational at an exciting growth period. Duties Responsible for ensuring manufacturing...

Summary: Our client is a biopharmaceutical company based in Carlow looking for a Senior Validation Engineer to join its team for a significant expansion project transitioning the new facility from construction & project phase to a commercialisation of fully operational facility delivering life-saving products to patients. Responsibilities: Vial and Syringe...

Quality Control Technician AS22683 Contract 11 months Were currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Carlow. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do. Reporting into the Quality Control Manager/ Associate...

This is a 12-month contract with a view to extension. Purpose The role will require the leadership of an experienced, energetic, and committed Senior/ Lead Engineering (CQV/ Technical Engineer) with broad experience in Vial and Syringe Filling operations and the below key areas. Vial and Syringe Sterile operations Isolators, VHP, decontamination systems....

Senior Validation Engineer 12 month contract On site Carlow AMC22531 Start date ASAP I am looking for an experienced Equipment Validation Engineer to support the transition of a new biomanufacturing facility from project phase to a fully operational manufacturing facility. This role would be suitable for a CQV/lead Engineer with 6+ years experience in Vial...

The role: PE Global is currently recruiting for a Senior CQV Engineer on behalf of a leading pharmaceutical company based in Carlow. This is an initial 12-month contract role. Description: An exciting opportunity has come to join the science, engineering/ manufacturing & commercialisation team to support the transition of the new facility from construction &...

LOCATIONCarlow & Ennis ROLE SUMMARY (purpose) To provide best in class engineering design and project management services to the operating business through innovate cost effective solutions, carried out in a safe and consistent manner throughout the business. Ensure engineering projects are delivered to budget and in compliance with company Health & Safety...