I'm looking for...

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.

Google Chrome
Internet Explorer
Mozilla Firefox

Your browser will need to close to complete the installation and you will need to manually reload the site when finished
Contact Info
Libby O'Donoghue
Life Science

+353 1 507 9254
[email protected]
Connect with me on
QC Scientist
Head of R&D
Process Engineer
Project Engineer
QC Manager
Validation Lead
R&D Manager
Quality Engineer
Process Engineer
Dublin North
Senior R&D Engineer
Limerick City
Apply for this job






Salary Expectations:



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 [email protected]

Process Scientist-Associate Manager LO(A008014)

Reference:A008014 Location: Limerick
Qualification:DegreeExperience:5-7 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: Scientist

Summary:Lead a team to manage all activities to ensure that manufacturing processes are supported. Responsible to support the Process Sciences Department through Process Validation, manufacturing floor support, product impact assessments, investigations, and technical evaluation as required. Active member of the Process Sciences management team.

Essential Duties and Responsibilities include, but are not limited to, the following:
• Lead a team and manage all activities to assure that manufacturing processes are supported.
• Responsible for developing a team such as development plans, upskilling and team forming.
• Write, review and approve Process Validation protocols and reports.
• Identification of process parameters and appropriate ranges to be included in process validation.
• Provide on the floor support to Manufacturing (Cell culture and Purification)
• Lead/Participate Process and Quality risk assessments.
• Lead troubleshooting activities associated with the manufacturing process.
• Provide technical support for manufacturing personnel to improve understanding of both cell culture and purification operations.
• Review and approve manufacturing documentation such as manufacturing records, SOPs and batch sheets.
• Develops/writes/plans and reviews protocols and activities for manufacturing support.
• Serves as a subject matter expert (SME) for data trending and manufacturing support.
• Presents and reviews process monitoring data to IOPS Management as necessary.
• Investigates and reviews OOS and OOL IPCs investigations.
• Performs, reviews and approves product impact assessment.
• Performs, reviews and approves scientific investigations (EOE & DNF).
• Communicate information on current process data and other IOPS initiatives which may impact process development and/or technology transfer.
• Support the site through regulatory audits by providing technical expertise.
Work efficiently and effectively in a fast-paced team-oriented environment to ensure maximum and high-quality output.

Education and Experience:
• BS/BA in a related field with 6+ years of related experience in a GMP environment. Previous experience in biological drug substance (DS) manufacturing.

For more information please contact Libby O'Donoghue on 0871897333 or [email protected]