CareerPlan

Study Lead - Pharma

Athlone, IrelandFull-time2026-10-02 → 2026-11-10
On-site · IrelandVisa sponsorship offered

Core

Managing multiple routine pharmaceutical testing projects (release, stability, quality control) in a GMP laboratory setting, ensuring data integrity and regulatory compliance.

Role type

Senior IC analytical study lead

Builds

Routine study outputs including reports, protocols, and quality records for pharmaceutical clients

Domain

Pharmaceutical industry + analytical chemistry

Required skills

HPLC operation, study design, analytical method development, GMP compliance, data trend analysis, risk assessment, technical troubleshooting, team mentoring

Preferred skills

Data collection software proficiency, process improvement strategies, audit readiness support

Technologies

HPLC, data collection software

Responsibilities

Manage multiple routine projects and communicate status updates to clients and stakeholders; Review and evaluate data, write scientific reports and protocols, and maintain quality records; Provide guidance and training to laboratory staff on routine test execution; Monitor daily operations for SOP and regulatory adherence; Escalate non-routine or complex technical issues to senior staff; Support audit readiness and participate in client audits.

Seniority

Senior, hands-on IC