Lead Analyst, Analytical Development (GMP)

LabRulez

Ringaskiddy

Remote

EUR 65,000 - 90,000

Full time

3 days ago
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Benefits offered by this job

Pension Plan
Life Assurance
Healthcare Plan
Annual Leave
Career growth opportunities

Job summary

Eurofins Scientific in Ireland (Ringaskiddy) is seeking an Analytical Development Days Lead Analyst to oversee a high-performing lab team, drive quality and client service, and coordinate scheduling and cross-training.

You will review GMP-compliant documentation, mentor staff, act as a key client contact, and contribute to continuous improvement initiatives while delivering on time and to the highest standards.

Qualifications

  • Degree or diploma in chemistry or a related subject.
  • Experience in a pharmaceutical industry GMP laboratory.
  • Experience in a leadership capacity.
  • Strong documentation skills and attention to detail.
  • Excellent communication and client service mindset.

Responsibilities

  • Act as site leader for the B shift on weekends (if shift lead).
  • Lead and coordinate a high-performing laboratory team, driving productivity, quality, safety, and customer service excellence.
  • Build strong client relationships and ensure service delivery meets or exceeds expectations.
  • Coach and develop team members through training, mentoring and feedback.
  • Manage scheduling, resource planning, and cross-training to maximise efficiency and achieve SLAs.
  • Review, approve, and maintain GMP-compliant technical documentation, data, SOPs and reports.
  • Contribute to continuous improvement initiatives using metrics and technical expertise.
  • Oversee QBAS as lead checker and schedule (if shift lead).

Skills

Leadership
Teamwork
Organization
Documentation
Communication
Quality
Client service

Education

Chemistry degree

Job description

Eurofins Scientific in Ireland (Ringaskiddy) is seeking an Analytical Development Days Lead Analyst to oversee a high-performing lab team, drive quality and client service, and coordinate scheduling and cross-training.

You will review GMP-compliant documentation, mentor staff, act as a key client contact, and contribute to continuous improvement initiatives while delivering on time and to the highest standards.

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