Equipment and Process Validation Lead

Job Description: Validating Medical Device Manufacturing ProcessesWe are seeking a highly skilled Senior Manufacturing Engineer to lead our validation efforts for medical device manufacturing processes. As a key member of our team, you will ensure that all manufacturing processes adhere to strict quality and regulatory standards.You will work closely with...

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...

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...

**Role Description**We're currently recruiting for a highly skilled 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...

We're looking for a skilled Validation Engineer to join our Quality Systems team in Limerick. As a key member of our organization, you will play a crucial role in ensuring the validity of our medical devices.About Life Science RecruitmentWe're an award-winning organization dedicated to providing exceptional recruitment services to the Life Sciences industry....

About Cpl HealthcareCpl Healthcare is a leading provider of healthcare professionals and managed services, dedicated to advancing healthcare by bringing life-changing medicines to patients worldwide.Our biopharma client based in Limerick has a long history of innovation and excellence, with a state-of-the-art Biotech Drug Substance Manufacturing Facility...

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...

Validation & CSV Lead Engineer Job Type:Permanent Location:Limerick, Ireland (Fully Onsite) The Role The validation leadshould be able toguide the team in creating the master validation plan (MVP), Validation strategy, Creating the validation output document (FAT, SAT, IQ OQ PQ) aligning to business SOPs.The client is seeking to validate a new machinewhich...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana, and our employees work together to discover and bring life-changing medicines to those who need them.We are seeking a Computerized Instrument Validation Lead to join our team at our Next...

Job Description: Senior Manufacturing Engineer (Test Method Validation)The ideal candidate will develop and execute Test Method Validations for Test Equipment per current QMS/Regulatory standards. This includes validating and implementing medical device manufacturing processes as assigned, identifying equipment/fixture installation qualification...

At Lilly, we unite caring with discovery to make life better for people around the world.We are a global healthcare leader headquartered in Indianapolis, Indiana.Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

The Eli Lilly and Company team is seeking a highly skilled Process Automation Lead to join our organization. As a key member of our manufacturing team, you will be responsible for providing technical leadership and expertise for automation support of manufacturing operations in accordance with Good Manufacturing Practices (GMP) and safety guidelines.This...

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...

NIRAS Ireland is a leading provider of project management, engineering design, and project resourcing services to the pharmaceutical and life science sectors. We specialize in designing and delivering process-driven projects, and we are committed to building long-term partnerships with our clients.About the Position:This role will involve working closely...

**Job Overview**In this critical role, you will be responsible for spearheading the design, specification, and commissioning of new and renovated biopharmaceutical process equipment. Your expertise will ensure seamless integration of cGMP process equipment, piping, and controls.Manage small-to-mid-sized projects related to process equipment and...

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,...

About the RoleWe are seeking a highly motivated Process Validation Engineer to join our team in Limerick.The successful candidate will be responsible for executing SIP/cleaning validation protocols, generating/reviewing/approving SIP/CIP protocols, and developing technical documentation.You will also be responsible for assessing SIP/CIP issues during study...

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,...

About Cpl HealthcareCpl Healthcare is a leading provider of healthcare professionals and managed services, dedicated to advancing healthcare by bringing life-changing medicines to patients worldwide.Our biopharma client based in Limerick is committed to excellence in manufacturing, with a state-of-the-art Biotech Drug Substance Manufacturing Facility...