Manufacturing QA Coordinator

Cognizant is seeking an agile and experienced CSV/QA Tester to join our collaborative team on a long-term contract basis. This full-time hybrid role based in Cork comes with a favorable salary and benefits package.As a CSV/QA Tester, you will assess software quality on newly purchased and existing QCL and production Lab Instruments. You will conduct testing...

Cognizant is seeking an agile and experienced CSV/QA Tester to join our collaborative team on a long-term contract basis. This full-time hybrid role based in Cork comes with a favorable salary and benefits package.As a CSV/QA Tester, you will assess software quality on newly purchased and existing QCL and production Lab Instruments. You will conduct testing...

About the RoleThis is an exciting opportunity for a Senior Quality Control Specialist to join our team at TN Ireland. The successful candidate will be responsible for managing QA GxP documentation, coordinating site training, and participating in internal audits.The ideal candidate will possess knowledge of current Good Manufacturing Practices (cGMPs), OPEX...

Job DescriptionA QA Specialist is required on an initial 12-Month basis by CareerWise Recruitment for our Cork-based multinational research-based pharmaceutical Company. This role is a QA Specialist II, in the GSIUC QA Department, under the QA General Operations Support team. This specific role is required to perform QA review of manufacturing and...

We are seeking an experienced Pharmaceutical QA Expert to join our team at Scientificjobs. As a key member of our QA Product Quality Team, you will play a crucial role in ensuring the highest standards of quality and compliance within our organization.In this role, you will manage and drive the site QA systems in close cooperation with other specialists. You...

Job Description: The QA Technician at our Cork facility will provide QA support to a growing manufacturing site. The incumbent performs material and product inspections and releases; documents the reviews and approvals, identifies, and communicates to management instances where materials or products are non-conforming with cGMP and QA standards. This...

Job Description: The QA Technician at our Cork facility will provide QA support to a growing manufacturing site. The incumbent performs material and product inspections and releases; documents the reviews and approvals, identifies, and communicates to management instances where materials or products are non-conforming with cGMP and QA standards. This...

Who We Are BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality...

QA Team Lead Job DescriptionWe are looking for an exceptional QA Team Lead to join our Quality Team at Boston Scientific's Cork facility. As a key member of the team, you will be responsible for providing leadership and guidance to a team of Quality Technicians.Main Responsibilities:Team Leadership: Supervise a team of Quality Technicians and provide expert...

Job DescriptionA QA Specialist I (Packaging and Labelling Operations) is required on an initial 12-month basis by CareerWise Recruitment for our Cork-based multinational research-based pharmaceutical company. This is a contract role for a QA Specialist within the GSIUC QA Department under the QA packaging and labelling support team. The successful candidate...

Job Summary">We are seeking a highly skilled QA Validation Associate to join our team at Claran Consultants Ltd. As a key member of our team, you will be responsible for the review and approval of validation lifecycle activities in a GMP regulated environment.">Main Responsibilities">Apply a risk management approach to identify, categorise, prioritise,...

Who We Are BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality...

Who We Are BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality...

Who We AreBioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists, and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality...

Overview The Outsourced Technical Services (OTS) Department at PM Group partners with Global leaders across a range of industries to find the best people for their current and ongoing business needs. Partnering with PM Group and our clients means that you will gain unrivalled experience working with global brands. We are seeking a skilled and experienced QA...

Job SummaryWe are seeking an experienced QA Validation Specialist to join our Client Validation team in a GMP regulated environment. The successful candidate will be responsible for reviewing and approving validation lifecycle activities, developing validation plans, and coordinating cross-functional teams. This role requires strong organizational and...

Key ResponsibilitiesProvide strategic direction to the QA CDMO Operations department to ensure corporate objectives are met.Ensure manufacturing and QC adherence to company policies/procedures, regulatory licenses, industry standards, and GMP regulations.Represent QA during site health authority inspections and business forums, including MRB and site...

We are a global healthcare leader committed to making life better for people around the world. As a Stability QA Professional, you will play a critical role in ensuring the quality and regulatory compliance of our biopharmaceutical products within our state-of-the-art manufacturing facility.Your responsibilities will include developing and maintaining...

**Job Summary**We are seeking an experienced Production Shift Manager to lead the shift team at our client's Sterile manufacturing plant in West Cork.About the Role:The successful candidate will be responsible for managing the shift team to achieve production targets and maintaining high-quality standards.Main Responsibilities:Manage the shift team to...

About the RoleQuality Associate - GMP ManufacturingThis is an entry-level or junior quality role that would suit a QA professional with 6 -12 months experience in a GMP manufacturing site. The role is predominantly desk-based batch review work.You will be responsible for ensuring the highest standards of quality control and compliance throughout the...