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
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

QC Analyst

Reference:JSC00000788 Location: Dublin
Qualification:DegreeExperience:See description
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: QC Analyst

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


The main areas of responsibility of this role are as follows:
• testing of routine release of raw materials, intermediates, finished product and stability as requested
• Draft and review documentation – SOPs, protocols, training modules, investigations, reports and QMS documents
• Actively participate in analytical method transfers and method validations as required
• Conduct and document out-of-specification/out-of-trend result investigations
• Responsible for the day to day running of the QC laboratory
• Experience with wet chemistry, GC, HPLC and a willingness to learn new analytical techniques as the laboratory evolves
• Work within the test schedule for the facility and the stability programmes
• Day to day activities required for running of the laboratory
• Self-starter with strong work ethic
• Good interpersonal skills are required, as is the ability to communicate well, both verbally and written.
• Must be able to function effectively in a teamwork environment
• Ability to identify, execute and prioritize work tasks/projects and know when to escalate
• Excellent problem-solving, decision-making and communication skills
• Good computer skills, including proficiency with business and technical software (Word, Access, Excel, PowerPoint, SAP, Empower)
• Ability to plan, organize, and prioritize effectively
• Good technical and compliance-based writing skills
• High levels of integrity and trustworthiness

Education & Experience

Minimum 3 years’ experience in a similar role
• Must include role(s) within a QC setting
• Experience of LCMS/MS and GC preferred
• Experience with method validation/ method development desirable
• Pharmaceutical drug/process development experience desirable