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Parexel

Scientist I, II or III Analytical Chemist

Ireland-Dublin

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hirly's read of this role

Seniority
Senior
Country
IE
Work mode
On-site / unstated
First seen by hirly
30 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

We are looking to fill a Scientist I, II or III - Analytical Chemist position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients located in Ireland . This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer any sponsorship.

Qualifications - B.S./M.S. in Chemistry, Biochemistry, Engineering, or a related discipline

Scientist 2 - B.S. with 1-2 years of relevant experience

Scientist 3 - B.S. with 3-5 years of relevant experience or M.S. with 1-2 years of relevant experience

Required Skills and Experience

Experience with GMP analysis using HPLC/UPLC including assay/impurity/etc., troubleshooting and data processing interpretation/analysis

Routine testing, data integrity assessments, investigative report authoring, and/or sample management responsibilities

Strong computer, scientific, and organizational skills

Clear communicator who speaks up about problems and improvement ideas

Able to manage multiple ongoing projects

Ability to work independently and as part of a team

Self-motivation, efficiency, adaptability, and a positive attitude

Desired Skills and Experience

Experience with Dissolution, Karl Fischer (KF), moisture testing and other wet chemistry skills

Empower software

Analysis of drug products

Good understanding of cGMP compliance requirements and ALCOA documentation principle

Overview

In the drug product registration stability testing lab, you’ll perform routine and stability sample analysis, SOP authoring, and day-to-day problem solving while contributing to new technologies and continuous improvement measures for optimized lab operations and other testing requirements. You’ll apply analytical characterization technologies and compliance principles to drive method robustness and high-quality stability data supporting late-stage pharmaceutical drug product development and commercialization. The ideal candidate is proactive, collaborative, and thrives in a compliance-focused environment.

About Parexel

Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies.

For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement.

Come join us!

#LI-DK1

Original posting on Parexel's site ↗

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