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

Process Engineer


Reference:SMC00028488 Location: Dublin
Qualification:DegreeExperience:1-2 Years
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Process Engineer, Bioprocess Engineer

Overview



This role will require the candidate to provide process development support primarily to the Forensics and Defect Laboratory. The candidate will establish themselves as an expert in forensic identification of Drug Product defects and maintain and produce extensive defect panels used to support automated and manual visual inspection of vial (liquid / lyophilised) and syringe packaged drug products.



Responsibilities



• Creation, Management and Maintenance of Inspection defect panels / sets.
• Execution of Knapp studies and data analysis.
• Establish experimental design, develop and implement protocols, obtain reproducible and reliable results and communicate data to cross functional groups.
• Ensuring all aspects of laboratory activity adheres to required policies and procedures, including safety and training.
• Ensure that the laboratory and site meet the quality requirements of its customers and applicable regulations (FDA, EU & international standards).
• Participate in cross functional teams at the site to ensure adherence to required policies and procedures and be responsible to deliver against organisational goals and project milestones.
• Assist in deviation and exception resolution and root cause analysis.
• Be accountable for the maintenance, distribution and upkeep of extensive defect panels used for the set-up, training and characterisation of automated / semi-automated / manual finished drug product visual inspection equipment.
• Provide process development expertise for commercial drug product particle / defect identification and contribute to the maintenance of local and global particle / defect libraries.

Basic Qualifications



• Third level bachelor’s degree in science, engineering or a relevant quality discipline with experience in a similar role OR Associate degree and directly related experience.
• Experience in Working in a Laboratory Environment.

Preferred Qualifications


• Be familiar with advanced microscopy (scanning electron microscopy) and spectroscopy (Fourier-transform infrared spectroscopy).
• Understanding of degradation mechanisms for biologics, analytical methods, laboratory practices, and basic statistical methods.

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

Sean McCarthy | Tel: +353 (0) 87 798 8480