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

Senior Manager Bioanalytical QC Lab


Reference:SCA014840 Location: Limerick
Qualification:DegreeExperience:5-7 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: Analytical Chemist, Analytical Group Leader, BD Manager, Biotechnician, Biotechnologist, Biotechnology Specialist, Quality Control Manager

Senior Manager Bioanalytical QC Lab
Our client, a global pharma company, are currently recruiting for a Senior Manager to lead the Bioanalytical Laboratory within the Quality Control Laboratory (QCL) team. This is a unique opportunity to help shape a next-generation facility from the ground up, integrating cutting-edge technology and data-driven approaches. This is a permanent role based in Limerick. Previous people management experience is essential for the role.

Responsibilities:

  • Lead and direct the Bioanalytical team to meet analytical timelines, ensure regulatory compliance, and continuously improve lab quality systems
  • Set annual objectives and performance metrics; drive strategic goals through effective leadership
  • Recruit, mentor, and develop a high-performing team
  • Oversee training programs, career development plans, and performance reviews
  • Review and approve quality documentation in accordance with procedures
  • Collaborate with site and external digital teams to design, build, and maintain QCL digital systems
  • Foster a culture of safety, compliance, and scientific excellence
Requirements:
  • BSc, MSc, or PhD in Analytical Sciences (e.g., Chemistry, Biochemistry, Microbiology)
  • Minimum 3–5 years of supervisory experience in a cGMP pharmaceutical or biotech environment
  • Deep knowledge of cGMPs and pharmaceutical laboratory regulations
  • Hands-on experience with analytical techniques including:
    • Immunoassays
    • Quantitative PCR
    • Chromatography
    • Capillary Electrophoresis
    • Spectroscopy
  • Strong understanding of data integrity principles and their application in a digital laboratory setting

For more information please contact Sinéad Cullen on +353879500821 or [email protected]