Associate Scientist

About the Role

An exciting opportunity is available for an Associate Scientist to join the Dundalk QC team, contributing to the Site Analytical Sciences organization within Global Quality, Large Molecule Analytical Sciences. This role is based in a rapidly expanding, dynamic start-up environment utilizing advanced technology.

The position involves supporting release and stability testing, executing and troubleshooting analytical methods, facilitating the transfer and verification of new methods, assisting with Digital Lab Records, and participating in continuous improvement and compliance initiatives within a regulated Quality Control setting.

Responsibilities

• Conducting and evaluating analytical data.
• Assisting with the digitalization program, including reviewing methods for Digital Lab Records implementation and re-qualifying equipment.
• Providing support for equipment qualification processes.
• Facilitating technology transfers from other company sites.
• Ensuring adherence to Good Manufacturing Practice (GMP) requirements during experiment and protocol setup.
• Maintaining compliance of all protocols and reports.
• Promoting and ensuring laboratory safety standards.

Requirements

• A minimum of a Bachelor’s degree in Chemistry, Biochemistry, Analytical Chemistry, Pharmaceutical Sciences, or a closely related scientific field.
• Demonstrated experience within the pharmaceutical industry.
• Practical experience with standard compendial methods such as pH, TOC, Karl Fischer titration, appearance assessment, and osmolality.
• Proficiency in Total Protein assays, Enzyme-Linked Immunosorbent Assays (EIAs), Polymerase Chain Reaction (PCR), or microbiological testing methods.
• A solid understanding of the product development lifecycle.
• Familiarity with regulatory filing requirements including Investigational New Drug (IND), Investigational Medicinal Product Dossier (IMPD), Marketing Authorisation Application (MAA), and Biologics License Application (BLA).
• Knowledge of current regulatory Good Manufacturing Practice (GMP) standards, including ICH guidelines and pharmacopeial requirements.
• A proactive, service-oriented, and communicative approach.
• Capability to troubleshoot technical issues and work autonomously.
• High levels of personal integrity, credibility, and enthusiasm.
• A commitment to Lean principles and continuous improvement methodologies.

Perks

The company is committed to flexible working arrangements where feasible, with a new hybrid working model introduced for office-based colleagues globally. Specific details regarding flexibility can be discussed during the application process.

Eligibility

This role is open to individuals with a relevant scientific degree and proven experience in the pharmaceutical sector. Candidates should possess practical skills in various analytical methods and a strong understanding of regulatory and GMP requirements. A proactive and independent work style is highly valued.

Additional Information

Our company in Ireland is a leading healthcare provider with a 50-year history, employing over 4,000 individuals across eight locations. We are dedicated to advancing manufacturing excellence and R&D through cutting-edge science and technology. The Dundalk site is a state-of-the-art vaccines facility focused on qualification, product development, and expanding capabilities, including drug substance and drug product manufacturing, and quality control labs to support global vaccine supply.

We prioritize the patient in all our endeavors, seeking solutions for challenging global healthcare needs. The company is an equal opportunity employer, valuing diversity and inclusion. Search firm representatives are advised that unsolicited assistance is not accepted, and fees are only paid under specific written agreements.

Employee Status: Regular

Job Posting End Date: 06/23/2026