QA Specialist

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 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...

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...

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...

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...

Quality Assurance Specialist Validation and NPI An amazing opportunity has arisen for a Quality Assurance Specialistto 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 validation...

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...

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...

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...

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...

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...

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...

Reporting to the QA Operations Manager and working as part of the QA Operations team, the successful candidate will be expected to carry out the role and responsibilities of the job function in an autonomous and responsible timely manner to meet all related targets and deadlines while maintaining good relations with, and flexibility within your team and...

PE Global is currently recruiting for QC Associate Microbiology Specialist on behalf of our client based in Carlow: 11 month initial contract A fantastic opportunity has arisen for a QC Associate Microbiology Specialist. You will provide technical support to the QC Microbiology Lab & operations to ensure the continued manufacture and supply of quality...

This is an 11-month initial contract. Purpose You will provide technical support to the QC Microbiology Lab & operations to ensure the continued manufacture and supply of quality pharmaceutical products in meeting the priorities of: Compliance, Supply, Strategy and Profit Plan. This role holds more senior responsibilities within the Microbiology Laboratory...

GerTEK is an engineering consultancy company specialising in project management, talent solutions and commissioning qualification and validation services. We partner with many of the world's largest life science & technology companies who entrust in us to deliver their most strategic and important projects with our technically strong personnel ensuring all...

Our client based in Sligo are looking to hire a QA Compliance Specialist on an initial 12 month contract. The Role: As the QA Compliance Specialist you will be responsible for documenting and establishing a quality system which ensures full compliance with all regulatory standards. You will be responsible for reporting on the effectiveness of the quality...

This is an 11-month initial contract. Purpose You will provide technical support to the QC Microbiology Lab & operations to ensure the continued manufacture and supply of quality pharmaceutical products in meeting the priorities of: Compliance, Supply, Strategy and Profit Plan. This role holds more senior responsibilities within the Microbiology Laboratory...

Company description: WuXi Biologics is a world-class biologics services provider (from discovery, through to commercialisation) with global clients in the biopharmaceutical and healthcare industries. Our mission is to accelerate and transform discovery, development and manufacturing in the fast growing field of biologics to benefit patients worldwide. The...