GMP Quality & Process Improvement Lead

i-Pharm Consulting; Haarlem; On-site; EUR 90,000 - 120,000; Full time

Job summary

i-Pharm Consulting is seeking an experienced Production Expert III to support pharmaceutical manufacturing in a highly regulated GMP environment. The role emphasizes quality oversight, deviation investigations, and continuous improvement across production activities.

The successful candidate will lead root cause analyses, drive CAPAs, review GMP documentation, and collaborate with QA, production leadership, and cross‑functional teams to ensure product quality and regulatory compliance.

Qualifications

• Master's degree in a relevant field as stated.
• Experience in pharmaceutical manufacturing.

Responsibilities

• Quality Assurance & Production Support across manufacturing.
• Lead root cause analyses and CAPAs for deviations.
• Support investigations relating to deviations and quality events.
• Review SOPs, validation protocols, batch records and GMP docs.
• Collaborate with QA, production leadership, and cross-functional teams.
• Support audits and compliance activities.

Skills

GMP knowledge

CAPA & root cause analysis

Quality Assurance

Investigations & deviations

Communication skills

Documentation & reporting

Education

Master's degree in Pharmacy, Chemical Engineering, Life Sciences, or related discipline

Job description

i-Pharm Consulting is seeking an experienced Production Expert III to support pharmaceutical manufacturing in a highly regulated GMP environment. The role emphasizes quality oversight, deviation investigations, and continuous improvement across production activities.

The successful candidate will lead root cause analyses, drive CAPAs, review GMP documentation, and collaborate with QA, production leadership, and cross‑functional teams to ensure product quality and regulatory compliance.