Cleaning Validation Specialist

Job Description A Cleaning Validation Specialist is required by Careerwise recruitment to work with our Limerick based Biotechnology client. Role of this position Generates, executes and/or reviews master and completed cleaning validation protocols, summary reports and associated data for conformance to regulations, SOPs, specifications and other...

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...

Job Description : SSE a CWS group company with over 20 years' experience is an award winning company that specialises in Cleanroom services, contract cleaning, facilities services and facilities audits. At SSE we operate within the Life Sciences Sectors, providing Cleanroom Cleaning & Contamination Control to Medical Device, Pharma, Software & Call Centre...

Technical Writer Cleaning Validation - Limerick - 12-Month ContractIreland is a hive of activity for the Life Sciences Sector at present with global players setting up new and expanding existing manufacturing facilities all over the Country. An exciting opportunity has arisen to work via Quanta on the client's side for a global Pharmaceutical organisation on...

Technical Writer Cleaning Validation - Limerick - 12-Month Contract Ireland is a hive of activity for the Life Sciences Sector at present with global players setting up new and expanding existing manufacturing facilities all over the Country. An exciting opportunity has arisen to work via Quanta on the client's side for a global Pharmaceutical...

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...

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...

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...

Job Description A Validation Executor (Cleaning Validation) is required by Careerwise recruitment to work with our Limerick based biotech client. 12 months contract position. Role of this position * Taking Cleaning Validation samples alongside Upstream/Downstream processing. * Working closely with manufacturing to ensure the CIP/SIP and dirty...

The role: PE Global is currently recruiting for numerous QA Cleaning Validation Engineers on behalf of a leading biotech company based in Limerick. This is an initial 12 month contract role. Responsibilities: Execution of cleaning validation protocols. Taking Cleaning Validation samples alongside Upstream/Downstream processing. Working closely...

Scientist – Process CleaningA Scientist – Process Cleaning is required to join a leading global Biopharmaceutical business based in Limerick. This is a fantastic opportunity to join a global business focused on developing and manufacturing breakthrough medicines. This is a fully site-based role on a brand new technically advanced manufacturing site and...

Scientist - Process CleaningAbout the RoleOur biopharma client based in Limerick is dedicated to advancing healthcare by bringing life-changing medicines to patients worldwide. Their state-of-the-art Biotech Drug Substance Manufacturing Facility in Limerick is designed to be one of the most technically advanced manufacturing sites in the industry, utilising...

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...

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...

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,...

Scientist - Process CleaningAbout the RoleOur biopharma client based in Limerick is dedicated to advancing healthcare by bringing life-changing medicines to patients worldwide. Their state-of-the-art Biotech Drug Substance Manufacturing Facility in Limerick is designed to be one of the most technically advanced manufacturing sites in the industry, utilising...

Working under the Quality Assurance organization this position is responsible for ensuring IT systems, programs and quality events are robust and meet regulatory agency expectations. The position will liaise with the IT and broader QA organizations to ensure all aspects of IT related programs are in compliance with regulatory agency expectations and internal...

Job Description A QA Validation Technical Writer is required by Careerwise recruitment to work with our Limerick based biotech client on a 12-month contract position. Role of this position Execution of SIP/ cleaning and continuing validation protocols. Writing and approving Deviations/ GMP documents Technical writing experience in writing site...

About 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 mission critical industries.Meeting a Higher Standard:Our...