Author average salary in Ireland, 2024

We are recruiting for a Safety Data Sheet Authorto join the Regulatory team in Naas. The SDS Author will be focusing on Chemical Safety and ensuring that products remain compliant with EU and Global chemical regulations. Expert level understanding of how to author a Safety Data Sheet from scratch fo...

Overview The Manufacturing Engineer 2 (Test Method Validation) Reporting to: Manager, Manufacturing Engineering Responsibilities Develop and execute Test Method Validations for Test Equipment per current QMS/Regulatory standards. Deputise for Senior Manufacturing Engineer (Test Method Validation) En...

Qualifications / Professional Skills / Knowledge Degree required:Level 8 bachelors related engineering degree: mechanical, manufacturing etc Proven experience:2-5years minimum experience, automated manufacturing experience an advantage Equipment qualification / validation desired Contact Information...

Translate Amgen requirements into the language of the CMO Identify and assess validation/quality risks to enable risk-based decisions Validation document author/approver Aseptic processing system oversight (media fill, autoclave validation, EM) Prepare materials/documents (playbooks) for topics to b...

Your new job Key duties & responsibilities include: Write and execute process validation protocols and report for new product introductions and revalidation due to process/material improvements Involved with the maintenance and support of compliance to IS0 13485 and ISO 14001 systems standards Incor...

Job Summary:The Validation Engineer will play a critical role in ensuring that all medical devices and associated processes meet quality, regulatory, and performance requirements. Perform process validation and re-validation activities to ensure continued compliance. Strong understanding of validati...

Provides Technical Writing assistance with the creation/updating of Documents. Provides Technical Writing assistance with the management of Change Controls,. Provides Technical Writing assistance with the completion of System Periodic Reviews. ...

I'm delighted to bring a new exciting opportunity for a Validation Engineer to take the step into a Senior role with one of Ireland's leading Biotechnology companies in Dublin on a 12 month contract. If you have 5+ years' experience in a similar Validation role with specific experience in equipment ...

Job Title:                                 Technical / BID Writer Location:                      
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The Validation Engineer will be responsible for reviewing and issuing of validation protocols and reports and also the co-ordination of the execution of validation activities (process / cleaning and equipment and computer qualifications) with the relevant departments. Here at Hays Life Sciences, our...

Technical Writer Cleaning Validation - Limerick - 12-Month Contract. Experienced Technical writer, . Technical writing experience has written a number of white papers and site reports. Technical writing experience for continuing assessments . ...

About the RoleAre you an HVAC/Validation Engineer looking for a new challenge? We have an exciting new opportunity for a HVAC/Validation Engineer based out of our site in Ballymount, Dublin. Role OverviewDelta-P Monitoring Technology Ltd, a Trescal company and a leader in the field of Cleanroom Vali...

A new and exciting opportunity for a Validation Engineer has come up with one of Cork's leading Medical Device companies on a 12 month hourly rate contract. You will need to have 4 years experience in a Quality or Validation role with knowledge of GMP regulations. Executing Commissioning, Qualificat...

PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide.We provide cloud-based software solutions for Quality Manage...

Refine technical jargon for clarity, persuasion, and a client-centric approach. Collaborate closely with technical specialists to tailor responses for tender requests. ...

Our site are excited to offer a fantastic Engineering Specialist (Validation) opportunity for candidates interested in a new challenge in a cGMP regulatory environment. Serve as validation representative for cross functional projects and represent the validation team at global technical forums. Filt...

Technical Writer - Cleaning Validation SIP. An experienced Technical Writer is required to become a key member of the Cleaning Validation team within a renowned Limerick based Biotech multinational. Technical writing experience has written a number of white papers and site reports. Technical writing...

IT Compliance Analyst (Technical Writer). Provides Technical Writing assistance with the creation/updating of Documents. Provides Technical Writing assistance with the management of Change Controls, Deviations, CAPAs. Provides Technical Writing assistance with the completion of System Periodic Revie...

I have a great new opportunity that just become available for a Technical Writer to join a reputable pharmaceutical company based in Limerick. Cooperate with Technical Owners to understand key critical information to support effective completion of technical records. Experience in Technical writing ...

Bridge to thousands of biopharma companies and their patients.Our investment is in People who make an impact, drive progress and create a better tomorrow.Our strategy includes building teams across our global network to pioneer and shape the future of PCI.Reporting to the Production Compliance Manag...

We are now seeking an Technical Report Writer to join on team on a fixed term basis (18-month contract). Reporting into the Asset Manager for Ireland, The Technical Report Writer will play a crucial role in the asset management department, providing operational support on various assets and DS3 serv...