Forgot your Password?
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

Technical Writer Senior


Reference:JSC0029002 Location: Dublin
Qualification:DegreeExperience:See description
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Senior Lecturer, Technical Writer

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 engineering, manufacturing, & inspection Standard Operating Procedures.
  • Liaise with Manufacturing/Inspection/Engineering regarding documentation changes in an effective and timely manner.
  • Develop protocols for execution in Manufacturing & Inspection in support of change controls, non-conformances & troubleshooting investigations with support from relevant SMEs.
  • Involvement in projects as part of continuous process improvement and / or troubleshooting.
  • Ownership of change controls for Manufacturing/Inspection/Engineering
    Issuance and updates of paper batch records in line with production schedule.
    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.
  • Provide technical and clerical support to the manufacturing, inspection & engineering teams in the preparation of documentation, collation of data and tracking of SOPs
  • Ownership of Level 1 non-conformances


Education & Experience

  • Educated to degree level or equivalent.
  • Significant experience in Chemistry/Microbiology/Engineering/Validation gained within a biotech, pharma or health care organisation.




If you would like further Information you can contact the recruiter directly:



Jack Caffrey | Tel: +353 (0) 1 507 9279