CareerPlanSign in

Compliance Manager

GBR - Northumberland - Cramlington💼 Full-time🗓 2026-09-21 → 2026-09-25

Core

Subject matter expert for GMP, quality, safety, and regulatory compliance driving a culture of quality and inspection readiness in pharmaceutical manufacturing.

Role type

Senior IC Compliance Manager (Pharmaceutical Manufacturing)

Builds

Pharmaceutical products via safe, reliable, and compliant manufacturing processes

Domain

Healthcare / Pharmaceutical Manufacturing

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

GMP knowledge, deviation investigation, CAPA management, change control, risk assessment, audit coordination, data integrity (ALCOA+), stakeholder management, continuous improvement

Preferred skills

Lean Six Sigma, regulatory inspection experience

Technologies

None stated

Responsibilities

Lead governance reviews and present compliance performance; drive health, safety, and environmental compliance; lead deviation investigations with root cause analysis; maintain inspection readiness; facilitate quality risk management; develop team capability through coaching and mentoring

Seniority

Senior, hands-on IC with leadership responsibilities

Sourced via workday · Listed on CareerPlan, which tracks 70,000+ jobs from 20+ sources.