Technical Author Jobs

McCloskey International - Dungannon

Summary As a Technical Author, you are required to deliver accurate and high-quality end user documentation and online parts content. You are expected to work as part of a dynamic team to contribute 30000.0

from: nijobs.ie - 8 days ago

Bristol Myers Squibb Irl - Dublin, County Dublin, Ireland

of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought

from: jobleads.ie (+1 source) - 7 days ago

Cork, County Cork, Ireland

scientific, technical, and drug discovery knowledge by reading the peer reviewed scientific literature, attending scientific conferences and via relevant training · Author or contribute to regulatory

from: jobleads.ie - 6 days ago

CPL Recruitment - London

from conception to submission. Job Responsibilities include; · Responsible, with limited guidance from the manager, for developing the technical eCTD sections to support Regulatory CMC dossier applications Negotiable

from: cpljobs.com - 2 days ago

Cork, County Cork, Ireland

approval process. Design/Author/Review/Approve/Execute Execution/development of change controls. Resolving technical issues encountered during study execution. Engagement with Production, Maintenance

from: jobleads.ie - 10 days ago

Ireland

/Approve/Executequalification/validation documentation and cycle development studies in linewith the standard approval process. · Design/Author/Review/Approve/ExecuteExecution/development of change controls

from: jobleads.ie - More than 30 days ago

Alexion Pharma International Operations - Dublin

for you! This is what you will do: As a Cleaning Validation Senior Technical Specialist, you will provide cleaning expertise in Upstream and Downstream equipment, author and review cleaning related documentation 12000.0

from: irishjobs.ie - 4 days ago

Cork, County Cork, Ireland

technical writing skills to author protocols, presentations and reports. Apply Univariate and/or Multivariate study design methodologies to discrete studies/experiments with appropriate support. Leverage

from: jobleads.ie - 27 days ago

Carlow, Ireland

/Execute qualification/validation documentation and cycle development studies in line with the standard approval process. Design/Author/Review/Approve/Execute Execution/development of change controls

from: jobleads.ie - More than 30 days ago

Claran Consultants Ltd - Cork

, distribution and handling methods, and any activities involved in properly transporting the drug throughout the supply chain. Review and approve artwork from a technical perspective. Author technical 70000.0

from: irishjobs.ie - 16 days ago