I'm looking for...
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
Contact Info
Administration Support
Dublin North
Biostatistician
Dublin City Centre
CSV Engineer
Dublin
Program Manager
Westmeath
Production Manager
Dublin City Centre
Consultant
Cork
Quality Manager
Dublin South
QA Specialist
Dublin
Quality Engineer
Dublin South
Process Engineer
Limerick
API Purchaser
Dublin
Risk Manager
Dublin
R&D Engineer
Dublin
Senior Social Work Practitioner
Republic of Ireland
Quality Engineer
Limerick
CTO
Galway
QC Trainer
Cork
R&D Engineer
Dublin
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

Validation Engineer


Reference:CK/A005756 Location: Australia
Qualification:DegreeExperience:2-3 Years
Job Type:Fixed Term ContractSalary: €60000 - €65000
May be suitable for: Validation Engineer, EHS Engineer

Validation Engineer

Our client, a global pharmaceutical leader is looking for Validation Engineers to join their team in Sydney, Australia.

The client will provide 6 month working holiday visas (with the potential for full sponsorship). They will provide assistance with relocation by providing visa, flight and temporary accommodation on arrival.

The client is one of the largest manufacturers of pharmaceutical products in Australia. At their state of the art manufacturing site they produce a range of sterile products that are being distributed to more than 30 countries. The site is going through an exciting growth phase with a multimillion dollar investment in the expansion of production lines.

Responsibilities:
• Write/develop validation protocols and reports (IQ/OQ/PQ/PPQ)for Capital Projects, Revalidation, OCM orCAPA which meet the requirements of established Testing Plans.
• Perform data analysis to evaluate process capability and make recommendations for process improvement where necessary.
• Develop risk assessments associated with validation activities, OCM or CAPAs
• As an SME, assist with review of validation test documents relating to OCM and CAPAs
• Ensure equipment systems and processes are appropriately validated in line with approved procedures, protocols and schedules.
• Assist with the review and enhancement of existing validation documentation, where appropriate.
• Keep up to date with developments within industry and cGMP requirements for validation.

What you can bring to the role:
• A degree (Bachelor, Master or PhD) in Engineering or Science (or related discipline)
• 3+ years in a pharmaceutical validation position
• Experience in Sterilization Validation and familiarity with CSV
• A deep understanding of PICS and GMP requirements
• Good report writing skills
• A can-do attitude, showing initiative and having a pragmatic mindset

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

Claire Kenny | Tel: +353 (0) 1 507 9287