Author average salary in Ireland, 2024

Basic Qualifications: Masters degree with 5+ years of experience in validation, engineering Or BS degree with 7+ years of experience in Validation, Engineering, Microbiology or Quality Preferred Qualifications: In-depth understanding and application of validation principles, concepts, practices, and...

This role would also be applicable to technical writers and copywriters with relevant experience. Technical Writer UX Designer - Contract Dublin. My client a global leading name is in urgent need of a talented and experienced UX designer and Technical Writer to join a client project for a rolling co...

The TECHNICAL WRITER, COMPLIANCE will work in the Technical Operations department and will facilitate reviews and revisions of Department related SOP's, life cycle documents, plans and policies for each group within the Department. TECHNICAL WRITER, COMPLIANCE required by CareerWise Recruitment for ...

Who we are ; Established in 2001, Eirdata are specialists in cleanroom validation, commissioning & compliance. ESS Group includes three companies Engineering Support & Services Ltd. Eirdata are specialists in cleanroom validation, commissioning and compliance, HVAC systems, indoor air quality and bu...

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 ...

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. ...

A QA Validation Technical Writer is required by Careerwise recruitment to work with our Limerick based biotech client on a 12-month contract position. Technical writing experience in writing site reports. ...

County Waterford, Republic of Ireland.Act as the quality representative for technical support, collaborating with other internal teams to address manufacturing issues for global customer accounts.Act as a bridge between the business and suppliers or customers on global quality matters.Create and sus...

As a technical writer, you will be an integral part of a software product development and release team, and will work closely with software engineers and other project stakeholders to develop software product content strategy for offline and online (web) use. You are expected to possess a Bachelor's...

The Quality Engineer (Validation) is responsible for implementing and maintaining the effectiveness of the Quality System. Responsible for reviewing, and approving all validation deliverables for Equipment, Facilities, Utilities, Software, Spreadsheets and Analytical validations at site. Must have a...

Must have Bachelor's or Master’s degree in a Life-Sciences or Engineering discipline. Must have a demonstrated background in Validation activities linked to Waste water management. ...

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...

Evaluate validation results of validation protocol executions and summarize validation results in final reports incorporating strong communication skills and experience. Creates and maintains validation documentation for new and existing systems and processes subject to design control. Ensures that ...

The Validation Engineer (Intern) has a key role in ensuring the on-going qualification and validation of equipment, systems and processes at Sanofi. Involved in the validation of new equipment, systems and processes at Sanofi. Generates validation documentation (protocols/reports) and provides assis...

We are looking to speak to a Quality Assurance Technical Writer that will contribute to our client's growth by revising and authoring documents that support the QA department. Quality Assurance /Technical Writer:. We are looking to speak to a Quality Assurance Technical Writer that will contribute t...

The PM Group now has an opportunity for a Validation Engineer (with isolator experience), to work on-site with a pharmaceutical client based in Carlow. Responsibilities To lead and/or support validation projects and activities on site, as directed and as appropriate. To prepare validation plans in l...

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 (Engineering). My client, a global Biotech company based in Limerick is looking to hire a Technical Writer on a contractual basis. The role will see you support the Engineering department and create technical documentation with support from the Project Engineers. ...

Computer Systems Validation Engineer . The validation and operational management of computerized systems. The creation and review of validation documentation in accordance with regulatory requirements and divisional policies. Engineering/Manufacturing/Science is preferred. ...

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...