Quality Compliance Lead – Sterile GMP Operations

Grifols, S.A; Dublin; On-site; EUR 60,000 - 80,000; Full time

Job summary

A global healthcare company is seeking a Quality Compliance Supervisor in Dublin to oversee quality compliance in Albumin Manufacturing. The candidate should have a minimum of 5 years in the pharmaceutical quality field, with a focus on EU GMP regulations. The role requires strong leadership, comprehensive compliance oversight, and technical expertise in sterile manufacturing. Competitive salary and career development opportunities are offered.

Benefits

Highly competitive salary

Group pension scheme

Private Medical Insurance

Ongoing opportunities for career development

Wellness activities such as Summer Events

Qualifications

• Minimum 5 years’ experience in a pharmaceutical quality environment under EU GMP regulation.
• Working experience within a Sterile Pharmaceutical GMP‑regulated industry.
• Demonstrated experience with Deviations, Investigations, and CAPAs.

Responsibilities

• Ensure compliance with all Training and Health & Safety requirements.
• Provide operational leadership and performance management.
• Author and review compliance-related documentation.

Skills

Problem-solving mindset

Project management skills

Leadership skills

Verbal and written communication in English

Familiarity with EU GMP regulations

Education

Bachelor or Master’s degree in Pharmaceutical Sciences or Administration

Tools

Veeva Vault

Trackwise

SAP

KNEAT

LIMS

Job description

A global healthcare company is seeking a Quality Compliance Supervisor in Dublin to oversee quality compliance in Albumin Manufacturing. The candidate should have a minimum of 5 years in the pharmaceutical quality field, with a focus on EU GMP regulations. The role requires strong leadership, comprehensive compliance oversight, and technical expertise in sterile manufacturing. Competitive salary and career development opportunities are offered.