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
Angela McCauley
Life Science

+353 87 696 0951
[email protected]
Connect with me on
R&D Engineer
Clare
Project Engineer
Limerick
Project Manager
Limerick
Quality Specialist
Tipperary
Manager R&D
Connaught
Recruitment Consultant
Republic of Ireland
R&D Director
Galway
R&D Manager
Galway
Senior Recruitment Consultant
Republic of Ireland
R&D Engineer
Clare
Project Enginer
Dublin South
R&D Manager
Connaught
Product Lead
Dublin
Senior Recruitment Consultant
Republic of Ireland
R&D Engineer
Galway
R&D Engineer
Galway
R&D Director
Galway
R&D Engineer
Galway
R&D Engineer
Dublin
Responsible Person (RP)
Republic of Ireland
CQV Lead
Tipperary
Account Manager UK and Ireland
Republic of Ireland
R&D Manager
Galway
Project Engineer
Republic of Ireland
R&D Manager
Connaught
Process Engineer
Limerick
Biostatistician
Dublin City Centre
Chemical Engineer
Tipperary
R&D Engineer
Galway
Head of R&D
Galway
Senior Quality Engineer-Remote
Republic of Ireland
Senior Manufacting Engineer
Republic of Ireland
R&D Manager
Galway
R&D Engineer
Galway
R&D Manager
Connaught
C&Q Lead
Tipperary
QA Engineer
Leitrim
QA Manager
Canada
Process Chemist
Limerick
R&D Director
Galway
R&D Engineer
Dublin
QA Manager
Canada
R&D Manager
Connaught
Medical Device Director
Republic of Ireland
R&D Manager
Galway
Project Engineer
Tipperary
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 [email protected]
Details

Cleaning Validation Engineer


Reference:AMC9772 Location: Carlow
Qualification:DegreeExperience:See description
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Validation Specialist

Cleaning Validation Engineer
AMC197
11 month contract
Carlow

I am currently on the look out for a Cleaning Validation Engineer for a Biopharmaceutical manufacturing plant in Carlow. This is the perfect role for someone with Cleaning validation experience looking for their next contract.

Responsibilities:

  • Ensure that site cleaning practices adhere to external auditing standards.
  • Act as the Subject Matter Expert (SME) for cleaning compliance activities on-site.
  • Coordinate with cross-functional teams to align local Standard Operating Procedures (SOPs) making updates as necessary.
  • Monitor and analyze cleaning deviations, creating annual action plans to enhance overall performance.
  • Lead cleaning improvement projects, clearly communicating progress on these initiatives.
  • Support investigations related to daily cleaning issues, ensuring that Corrective and Preventive Actions (CAPA) are in place to prevent recurrence.
  • Participate in or lead the Cleaning Community of Practice, collaborating across four API sites within the company's network.
  • Work alongside internal and external stakeholders, including Compliance Owners, to facilitate investigations, implement improvements, manage change controls, and develop CAPAs.
  • Lead complex investigations with cross-functional teams by applying analytical and problem-solving skills to identify root causes, assess impacts, and execute process enhancements.

Requirements
  • PhD in Chemistry, BE/ME Chemical Engineering, Pharmaceutical Sciences, or related field.e.
  • Minimum of 2 years of experience in a similar role within the pharmaceutical industry or equivalent.
  • Strong understanding of cGMP regulations and experience in supporting investigations and regulatory audits.
  • Excellent communication and collaboration skills, with the ability to lead cross-functional teams and drive process improvement initiative


If you are interested in this or similar roles apply today and Angela will be in touch if you are good fit