Analytical Chemist, Cork

Analytical Chemist with Reviewer Ballydine, Co. Tipperary Contract Duration: 11 Months Initially Day Role | Fully Onsite | No Shift Role Overview We are seeking an Analytical Chemist to provide laboratory testing and analytical support within a GMP-regulated pharmaceutical manufacturing environment. The role will support late-stage clinical and commercial drug product testing across raw materials, intermediates, API, and finished products.

The successful candidate will perform analytical testing using approved methods and pharmacopoeia standards while ensuring compliance with GMP, laboratory procedures, and regulatory requirements.

Key Responsibilities

Perform analytical testing of raw materials, intermediates, API, and finished products using approved methods and pharmacopoeia procedures.

Ensure all laboratory activities are completed in compliance with GMP and safety requirements.

Review analytical results for accuracy and compliance with specifications and test methods.

Document laboratory activities accurately within computerized laboratory systems.

Support laboratory investigations, root cause analysis, CAPA activities, and troubleshooting.

Prepare and revise laboratory documentation including SOPs, protocols, reports, and procedures.

Operate, maintain, and troubleshoot laboratory equipment where required.

Participate in continuous improvement initiatives and method enhancement projects.

Support method transfers, introduction of new analytical techniques, and validation activities.

Collaborate effectively within cross‑functional teams to support project timelines and business objectives.

Assist in training and mentoring laboratory personnel where required.

Required Experience&Skills

BSc degree (or equivalent) in Analytical Chemistry, Pharmaceutical Science, Chemistry, or related scientific discipline.

Experience working within a GMP-regulated pharmaceutical laboratory environment.

Strong knowledge of analytical laboratory techniques and cGMP requirements.

Experience with laboratory investigations, deviations, and documentation practices.

Good understanding of analytical instrumentation and troubleshooting.

Strong communication, teamwork, and problem‑solving skills.

Ability to manage multiple priorities and complete assignments within timelines.

Proficiency in computer systems such as Excel, Word, Outlook, and laboratory systems.

Preferred Skills

Experience in pharmaceutical drug product, API, or raw material testing.

Exposure to analytical method validation or method transfer activities.

Experience participating in continuous improvement initiatives.

Knowledge of regulatory requirements related to pharmaceutical analytical laboratories.

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