Technical Writer Jobs in Limerick
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Search Results - Technical Writer Jobs in Limerick
QA Resources-Limerick
Technical Writer (Assoc, Int, Sr)
Industry: Pharmaceutical
Department: Technical Operations – Engineering and Automation Compliance
Role Summary:
Performs all technical writer related tasks necessary for the creation and maintenance of quality...
Morgan McKinley-Limerick
Department: Technical Operations - Engineering and Automation Compliance
Contract Type: Hourly Rate Contract
We are seeking experienced Technical Writers of ALL LEVELS to join our Technical Operations - Engineering and Automation Compliance team...
morganmckinley.com -
Hero Recruitment-Limerick
Technical Writer (Assoc, Int, Sr)
Department: Technical Operations - Engineering and Automation Compliance
Summary: Performs all technical writer related tasks necessary for the creation and maintenance of quality GMP documentation in support...
appcast.io -
QA Resources-Limerick
look for Continuous improvements.
Experience in Validation specifically cleaning validation.
Experience in assessment of cleaning issues during study runs.
Experienced Technical writer.
Experience in Deviation/Change control writing.
Capable...
Regeneron Ireland DAC-Limerick
and industrial intelligence in relation to IOPS business practices Subject Matter Expert (SME) for authoring and developing the standards, policies and procedures in line with regulatory requirements and industry best practices Technical writing, research...
PE Global-Limerick
PE Global is recruiting for a Technical Writer on behalf of our pharmaceutical client in Limerick. This is an initial 12-month contract role. Summary: Performs all technical writer related tasks necessary for the creation and maintenance of quality...
Eli Lilly and Company-Limerick
submissions and the creation of related documentation.
• Excellence in technical writing and oral communication skills with the ability to effectively communicate and transfer knowledge to all levels of the organization.
• Work with scientists and engineers...
appcast.io -
PE Global-Limerick
improvements Experience: Experienced in QA Validation activities Extensive experience on writing and approving Deviations/GMP documents Technical writing experience in writing site reports Experience in aseptic technique Experience in Gowning for IOS7/ISO8...
Morgan McKinley-Limerick
QA Validation Consultant - Technical Writer
Location: Munster
Contract Type: 12-Month Contract (Limited or Umbrella Company)
Start Date: Immediate
4/5 days onsite
Join the largest bulk biopharmaceutical manufacturer in Ireland as a Technical...
morganmckinley.com -
Cook Medical-Limerick
experience in a supervisory position leading and motivating a group of talented engineering staff is desired. Proven project management skills. Strong technical writer. Good mechanical design, materials aptitude and understanding of engineering fundamentals...
PE Global-Limerick
for Continuous improvements Experience : Experienced in QA Validation activities Extensive experience on writing and approving Deviations / GMP documents Technical writing experience in writing site reports Experience in aseptic technique Experience in Gowning...
irishjobs.ie -
Limerick
skills.
• Strong technical writer.
• Good mechanical design, materials aptitude and understanding of engineering fundamentals with extensive medical device materials knowledge.
• Strong medical device experience with combination product.
• Extensive...
icims.com -
Morgan McKinley-Limerick
This role focuses on QA Validation activities, with a particular emphasis on SIP processes and thermal mapping. The ideal candidate will bring expertise in validation protocols, technical writing, and cross-departmental collaboration to ensure...
morganmckinley.com -
Limerick
in the medical device industry.
• Good technical background including technical writing skills.
• Knowledge of a GMP regulated environment and experience in a similar role would be an advantage.
• Previous experience in dealing with Complaints and Quality System...
icims.com -
Cook Medical-Limerick
ISO14971, the Medical Device Directive, EU Medical Device Regulation 2017/745 and the FDA QSR including 21 CFR Part 820 and 21 CFR Part 11, ideally gained in the medical device industry. Good technical background including technical writing skills...
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