Equipment Validation Professional

The Job DescriptionCleaning Strategy DevelopmentCreate and own the Cleaning Validation Master Plan for the facilityGenerate cleaning validation protocols and summary reportsExecute cleaning validation protocols, including visual inspection and sampling, and coordinate with other support groups (e.g. operations, maintenance, lab, etc.)Author cleaning...

We are looking for a Validation Support Professional to join our team at Eir evo talent. The successful candidate will have experience supporting the validation of major capital automation projects and be able to guide in transitioning from manual to automated validation methodologies.This role involves developing life cycle validation documentation and...

Key ResponsibilitiesThe Automation Engineer SME will be responsible for:Configuring and programming biopharma manufacturing equipment used in both upstream and downstream processes, as well as QC lab and analytical equipment.Leading the development and execution of validation protocols for computerized equipment.Providing expert guidance to internal...

About the RoleRéalta Technologies is seeking an experienced Automation Engineer SME to join our team. The successful candidate will have hands-on experience in configuring, validating, and programming biopharma equipment.The Automation Engineer SME will be responsible for providing expert guidance to internal validation teams and leading the development and...

We're currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Cork. 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.DutiesExecute cycle development, cleaning validation and PQ of equipment.Writing and adhering to validation...

We're currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Cork. 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.Duties1. Execute cycle development, cleaning validation and PQ of equipment.2. Writing and adhering to...

We are looking for an experienced Manufacturing Engineer II to join our team at Hero Recruitment. In this role, you will be responsible for ensuring that manufacturing processes meet the highest standards of quality, compliance, and efficiency.You will have the opportunity to develop and execute Test Method Validations (TMVs) to ensure the reliability and...

Job OverviewWe are seeking a highly skilled professional to lead our validation efforts.In this role, you will be responsible for developing and executing Test Method Validations to ensure compliance with quality and regulatory standards.Responsibilities:TMV Development: Develop and execute TMVs for test equipment, ensuring compliance with QMS and regulatory...

OverviewTN Ireland is a leading player in the Life Sciences Sector with a strong presence in Ireland. We are currently seeking an experienced Technical Writer to join our team on a major expansion project in the Munster region.Role SummaryThe successful candidate will be responsible for managing a large program, generating/reviewing/approving SIP protocols,...

Job Description:Key Responsibilities:Perform project management tasks for medium to large-scale projects involving new or existing equipment.Assist in determining the budget to support requirements.Evaluate technology necessary to support requirements.Propose options to stakeholders.Provide technical support for projects.Assist in negotiation with...

We're currently recruiting for an exciting opportunity with an award-winning Medical Device organization based in Limerick.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.DutiesProvide support for the validation activities associated with equipment, reagents, facilities,...

Hobson Prior is collaborating with a Biotech company who are in search of a Specialist in QA Validation. The chosen individual will offer supervision for the production and distribution of Gene Therapy medicinal products. They will be instrumental in guaranteeing that processes and equipment meet validation and qualification standards as per relevant...

We're currently recruiting for an exciting opportunity with an award-winning Medical Device organization based in Limerick. 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.Duties1. Provide support for the validation activities associated with equipment, reagents, facilities,...

Hobson Prior is collaborating with a Biotech company who are in search of a Specialist in QA Validation. The chosen individual will offer supervision for the production and distribution of Gene Therapy medicinal products. They will be instrumental in guaranteeing that processes and equipment meet validation and qualification standards as per relevant...

Validation EngineerIreland, Ireland/North Europe/Full TimeAbout CAI:CAI is a 100% employee-owned company established in 1996, that has grown year over year to nearly 700 people worldwide. We provide commissioning, qualification, validation, start-up, project management and consulting services related to operational readiness to FDA regulated and other...

**About the Role**We are seeking an experienced Validation Specialist to join our team at a leading pharmaceutical organization based in Ireland.The successful candidate will be responsible for executing cycle development, cleaning validation, and performance qualification of equipment. They will also write and adhere to validation strategies, coordinate...

About the Job:We are seeking a highly skilled Documentation Writer to join our team as a Validation Support Documenter & Technical Writer. In this role, you will be responsible for creating and maintaining technical documentation, including user guides, manuals, and SOPs. You will also support the validation of major capital automation projects and...

Job Description A Validation Technical Writer is required by Careerwise recruitment to work with our Limerick biotech client on a 12-months contracting position. Role of this position Generation of Summary Reports. Writing and approving Deviations/ GMP documents. Maintain and update Cleaning/ SIP Validation Plan. Schedule of Cleaning/ SIP...

Senior Validation & CSV EngineerThis person is responsible for leading validation teams' efforts for systems and processes to ensure compliance with industry standards and regulatory requirements. This role involves leading validation activities, developing validation strategies, executing test plans, analyzing data, and providing technical expertise to...

Job DescriptionIn this role, you will develop and execute Test Method Validations to ensure compliance with quality and regulatory standards.You will work closely with design, process, and quality teams to validate and implement manufacturing processes.Responsibilities Include:TMV Development: Develop and execute TMVs for test equipment, ensuring compliance...