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 [email protected]
Details

Commissioning and Qualification Engineer


Reference:SMC37495 Location: Cork
Qualification:DegreeExperience:See description
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: EHS Engineer, Validation Coordinator

We’re currently recruiting for an exciting opportunity with an award-winning pharmaceutical organization based in Cork. 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


• Provide Technical Support for the commissioning and qualification of laboratory equipment including equipment IOQ and PQ

• Work with site support groups to deliver qualified raw materials and consumables for the manufacturing process.

• Author, review and approve manufacturing documentation associated with transferred processes.

• Troubleshoot technical issues and lead investigations through scientific problem-solving approaches.

• Partner with quality groups to support change management to implement process improvements

• Generate study plans, protocols and summary reports

• Establish and lead implementation the continued process verification program to effectively manage product life cycles.

• Adherence to highest standards for Compliance (Quality and Safety)

• Ensure compliance with site EHS policy, cGMP and other business regulations and participate in risk assessments, audits, regulatory inspections and incident investigations.


Education & Experience


• Experience in a pharmaceutical or a highly regulated environment preferably with cGMP experience

• BSc Degree in Biochemistry, Microbiology, Chemistry, Engineering or a related field

• Experience in at least two of the following areas protein chemistry, process engineering, cell culture, purification technologies, process operations, statistics, technology transfer, microbiological control of bio-manufacturing processes, cleaning validation, process validation, regulatory inspections.



If interested in this posting please feel free to contact Seán McCarthy on +353 (0)87 798 8480 or [email protected] for further information.