close

Did you know that your Internet Explorer is out of date?

To get the best possible experience using our website we recommend that you upgrade to a newer version or download another web browser.
A list of the most popular web browsers can be found below. Just click on the icons to get to the download page.

crome
Google Chrome		 IE
Internet Explorer		 firefox
Mozilla Firefox		 opera
Opera

Your browser will need to close to complete the installation and you will need to manually reload the site when finished
Apply for this job

Name:

Surname:

Email:

Phone:

Cv:

Salary Expectations:

Education:

Experience:

Current Location:

Notice Period:

Write here your cover note:


If you would like us to create a jobseeker account for you, giving you access to
account management, job alerts and one-click applications, then please tick this box

If you are having difficulty you can always email your cv to applications@lifescience.ie
Details

Senior Technical Writer


Reference:RK3331 Location: Dublin
Qualification:DegreeExperience:1-2 Years
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Technical Writer

Senior Technical Writer
RK3331
12 Months
Dublin



We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Dublin. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.




Duties:

  • Develop, review and update manufacturing documentation.
  • Ownership of change controls for Manufacturing.
  • Liaise with Manufacturing regarding documentation changes in an effective and timely manner, rolling out one point lessons where necessary.
  • Maintain awareness and compliance with project timelines.
  • Develop protocols for execution in Manufacturing in support of change controls, deviations & troubleshooting investigations with support from relevant SMEs.
  • Support execution of protocols as required by project.
  • Involvement in projects as part of continuous process improvement and / or troubleshooting,
  • Liaise with Quality Assurance to ensure that GMP standards are maintained in line with current OS
  • Support production support team in reducing document turnaround times.
  • Use specified software packages and standard procedures, responsible for compiling and maintaining all relevant documentation including SOPs, APPXs, TRNQs.
  • Provide technical and clerical support to the manufacturing teams in the preparation of documentation, collation of data and tracking of SOPs
  • Ownership of minor deviations as required



Education and Experience :
  • Educated to degree level or equivalent.
  • Experience in Chemistry/Microbiology/Engineering/Validation gained within a biotech, pharma or health care organisation.

If interested in this posting please feel free to contact Rachel Kent on +353 (0)87 427 8808 or rachel.kent@lifescience.ie for further information.