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Analytical Sciences & Technology (AST) Analyst

Contract
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Ireland
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Pharmaceutical / Biopharmaceutical
Manufacturing, Engineering and Production
Specialist
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Description

Analytical Sciences & Technology (AST) Analyst


Role Summary:


A leading organisation in the pharmaceutical sector is seeking an Analytical Sciences & Technology (AST) Analyst to support key analytical projects and ensure compliance with Good Laboratory Practices (cGLP). This role presents an exciting opportunity to contribute to method development, qualification, and troubleshooting within a dynamic and collaborative environment.

As a vital member of the AST team, you will work closely with cross-functional departments, including Quality Control (QC), Quality Assurance (QA), Manufacturing, and Technical Services, to support ongoing projects and drive continuous improvements in analytical methodologies.

Key Responsibilities:


Analytical Support & Method Development
Provide analytical chemistry expertise to support AST-MSAT and broader site activities.
Participate in the development, qualification, and optimisation of analytical methods.
Support method transfer activities as required.
Assist in analytical troubleshooting, investigations, and functional method improvements.
Contribute innovative ideas and research advancements in analytical sciences.


Collaboration & Cross-Functional Engagement
Work closely with key internal stakeholders, including QA, QC, Manufacturing, Engineering, and Program Leads, to ensure seamless project execution.
Provide regular updates on ongoing projects, highlighting potential challenges and areas for improvement.
Assist in training analysts in new methods, techniques, and areas of expertise.


Compliance & Quality Assurance
Ensure laboratory operations align with current Good Laboratory Practices (cGLP) and regulatory standards.
Maintain compliance with current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP).
Ensure that laboratory equipment and critical chemical testing processes meet validation requirements (IQ/OQ/PQ).
Support audit readiness by maintaining high compliance and safety standards.


Qualifications & Experience:


Education & Background
Degree in Science (Chemistry or Biochemistry preferred).
Experience in a laboratory environment, ideally within the pharmaceutical or biopharmaceutical sector.


Skills & Knowledge
Strong operational experience within quality laboratories in a fast-paced manufacturing environment.
Familiarity with quality management systems, pharmacopeial methods, and stability testing.
Comprehensive understanding of GMP, cGLP, and compliance regulations.
Ability to manage projects within timelines and budget.
Strong grasp of Key Performance Indicators (KPIs) within a pharmaceutical setting.


Leadership & Personal Attributes
Excellent communication and facilitation skills.
Ability to work independently while contributing to team goals.
Demonstrates flexibility, drive, and a proactive approach to problem-solving.
Commitment to business needs and continuous improvement.
Ability to collaborate effectively with cross-functional teams.
Eager to learn new techniques and contribute innovative solutions.


Why Join Us?
Work with leading pharmaceutical organisations in a collaborative and evolving environment.
Gain hands-on experience in method development, qualification, and analytical troubleshooting.
Opportunity to contribute to high-impact projects in a compliance-driven setting.
Be part of a dynamic team that values innovation, quality, and professional growth.


This role offers a fantastic opportunity for an analytical professional looking to enhance their expertise and make a meaningful impact in pharmaceutical sciences.

If you’re ready to take the next step in your career, we’d love to hear from you!