GMP Compliance Lead (Fixed-Term) – Onsite Biopharma Ops

Boehringer Ingelheim GmbH; Ash; On-site; GBP 60,000 - 85,000; Full time

Job summary

Boehringer Ingelheim GmbH in Pirbright, Surrey, is seeking a Production Compliance specialist to uphold GMP readiness and support quality systems across manufacturing operations. The role focuses on leading deviation investigations, CAPA and change control, delivering training, and partnering with QA to maintain audit-ready documentation.

The fixed-term position runs until December 2027 with a requirement to be on site at least three days a week, offering exposure to biosafety, EHS, and

Qualifications

• Strong knowledge of GMP and quality systems.
• Experience in aseptic manufacturing or biology products.
• Ability to manage multiple priorities in a fast-paced environment.

Responsibilities

• Lead deviation, CAPA and change control activities with timely investigations.
• Provide compliance support to production teams and QA.
• Drive improvements via the change control system.
• Develop and deliver compliance training and documentation.
• Collaborate with QA and cross-functional teams for audits.
• Support risk management and EHS related activities.

Skills

GMP knowledge

Quality systems

CAPA

Change control

Investigations

Aseptic manufacturing

Regulatory knowledge

Education

Science degree

Tools

Microsoft Office

Job description

Boehringer Ingelheim GmbH in Pirbright, Surrey, is seeking a Production Compliance specialist to uphold GMP readiness and support quality systems across manufacturing operations. The role focuses on leading deviation investigations, CAPA and change control, delivering training, and partnering with QA to maintain audit-ready documentation.

The fixed-term position runs until December 2027 with a requirement to be on site at least three days a week, offering exposure to biosafety, EHS, and