Implements policies and procedures to validate/qualify equipment, systems, and processes in accordance with regulatory requirements and company manufacturing standards. Essential Duties and Responsibilities include, but are not limited to, the following: • Generates, executes and reviews master and completed qualification and validation protocols, summary reports and associated data for conformance...

Microbiology Analyst – Limerick. The Scientist 1 Micro and Scientist 2 Micro roles are responsible for assuring that non-conformance investigations, laboratory investigations and quality systems follow the good manufacturing practices and good laboratory practices as established in the code of local government regulations and company procedures. 2.Responsibilities: List main...

A QA Senior Specialist - External DP Manufacturing is required by CareerWise Recruitment for our Limerick based client. This is an opportunity to join a select team with our major Limerick based Biopharma multinational client. THE ROLE: * Perform activities in support of dispositioning product while ensuring compliance with Quality...

QA Specialist required by CareerWise Recruitment for our Limerick based client. CareerWise Recruitment has been retained by a top multinational in Limerick with a well-known brand name. We are partnering with them to recruit a QA Specialist (Batch Release) with 3 years' experience to join their team on a permanent...

SIP SPECIALIST required by CareerWise Recruitment for our multinational BioTech client in Mid-west (Ireland. The SIP VALIDATION SPECIALIST will be involved in the review and approval of SIP thermal mapping and Performance Qualification validation protocols, extensive experience on writing and approving Deviations requiired. THE ROLE. * Experience in Validation specifically...

Quality Inspector / Regulatory Associate – Successful Medical Supplier. Limerick. €Excellent DOE. If you are a qualified quality professional looking to take your next step, this is a brilliant opportunity to help a pioneering business maintain their reputation for excellence. Our client is a leading supplier of medical devices...

Senior Regulatory Affairs Specialist. The regulatory affairs specialist helps develop regulatory strategies, performs activities associated with obtaining and maintaining regulatory approval to commercialise medical devices in selected target markets. The regulatory affairs specialist serves as a communication liaison between the manufacturer and the local affiliates or regulatory authorities. Responsibilities: Assists...

Analytical Chemist Job Limerick Permanent. I currently have a fantastic opportunity for an Analytical Chemist to join a global company in Limerick. This is an excellent company which commits to giving all its employees opportunities for professional development and advancement. The main aim of the Analytical Chemist position is to...

On behalf of my client, a global medical device company, I am recruiting for a Senior Regulatory Affairs Co-ordinator . This is a European focused role in which you will be responsible for ensuring that products already on the market meet with the new medical device regulations. You will be involved...

Excellent opportunity for a QC Analyst- Environmental Monitoring to join a leading pharmaceutical company based in Limerick. Will consider applicants form a GMP food backgroud who would like to move into the pharma industry. Full time permanent- shift pattern- excellent salary benefits package. Contact Aoife on 086 044 3981. This...

An MES Operations Analyst is required by CareerWise Recruitment for our Limerick based client. This position will be responsible for the Design and Configuration of the Manufacturing Execution Systems (MES) manufacturing Batch Records and Equipment data. THE ROLE: * Design and deploy MES system (Werum's PAS-X) to replace paper based...

Regulatory Affairs Specialist opportunities with global medical device company! These are contract roles, approximately 1 - 2 years duration. In this role you will help develop regulatory strategies and perform activities associated with obtaining and maintaining regulatory approval to commercialise medical devices in selected target markets. Responsibilities will include the...

Regulatory Affairs Specialist opportunity with global medical device company! In this role you will help develop regulatory strategies and perform activities associated with obtaining and maintaining regulatory approval to commercialise medical devices in selected target markets. Responsibilities will include the following: Plan and prepare regulatory submissions for specific target markets...

One of the most dynamic and exciting manufacturing sites in Munster is seeking to add a number of MSAT Specialists to its high performing team and support Internal and External Tech transfer projects. If you`re passionate about science and relish the opportunity to work in a demanding but rewarding environment...

One of the most dynamic and exciting manufacturing sites in Munster is seeking to add a number of MSAT Specialists to its high performing team and support Internal and External Tech transfer projects. If you`re passionate about science and relish the opportunity to work in a demanding but rewarding environment...