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QC Analyst

QC Analyst

Reference: BBBH29215
Date posted: 04/06/2026
Job details
Specialism
Technical Operations
Expertise
Quality Control
Location
Tipperary, Tipperary, Republic of Ireland
Job type
Permanent
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Description

Ensure quality at every step-driving compliant, high-impact lab operations in a cutting-edge pharmaceutical environment.

R&D Partners is seeking a QC Analyst to join a leading pharmaceutical company in ROI. This role involves supporting laboratory setup activities, performing quality control testing, and ensuring compliance with cGMP and regulatory standards. The ideal candidate will have a strong background in analytical methods, laboratory operations, and quality assurance.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Support laboratory setup activities at the Cashel site.
  • Prepare laboratory procedures, specifications, protocols, and reports.
  • Perform laboratory testing and investigations per SOPs and cGMP requirements.
  • Conduct peer reviews of documentation as needed.
  • Execute analytical method verification, validation, and technical transfer.
  • Manage laboratory consumables, including ordering and tracking.
  • Assist in equipment qualification activities.
  • Collaborate with other departments and support laboratory colleagues daily.
  • Liaise with CROs on behalf of the company and conduct audits when appropriate.
  • Ensure audit readiness and support preparation for regulatory audits/visits.
  • Develop QC testing processes and maintain compliance with EHS governance.
  • Operate in compliance with global policies, procedures, and regulatory requirements.
  • Maintain a clean and organized work area to ensure product security.
  • Perform analytical balance calibrations and other tasks as defined in relevant SOPs.

Key Skills and Requirements:

  • Strong understanding of cGMP and regulatory compliance.
  • Experience in analytical method validation and technical transfer.
  • Familiarity with laboratory setup and equipment qualification.
  • Excellent documentation and Good Documentation Practice (GDP) skills.
  • Ability to collaborate across departments and support cross-functional teams.
  • Strong organizational and problem-solving skills.
  • Prior experience in a pharmaceutical or biopharmaceutical environment is preferred.

For more information, please contact Jessica Taylor.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you’ve read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.r-dpartners.com/privacy-policy/

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Register your interest

If you can’t find your ideal role with us right now, we’d still love to hear from you! Send us your CV and we’ll contact you if a suitable role becomes available.

Register interest

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