CareerPlan

GMP-Consultant (m/w/d)

Mannheim, BADEN_WUERTTEMBERGFull-time2026-10-04 → 2026-11-11

Core

Creating GMP-compliant SOPs and risk analyses, qualifying pharmaceutical equipment, and verifying process compliance.

Role type

GMP compliance consultant

Builds

Pharmaceutical production processes and equipment qualification

Domain

Life Sciences / Pharmaceutical Manufacturing

Required skills

GMP knowledge, SOP creation, risk analysis, equipment qualification, change control management, technical documentation review

Preferred skills

Process engineering background, quality assurance experience

Technologies

GMP standards, SOPs, risk assessment tools

Responsibilities

Create GMP-compliant SOPs and risk analyses, Qualify pharmaceutical equipment and document processes, Verify plant and process compliance, Coordinate maintenance and calibration activities, Review technical documents for changes and deviations, Support change control and deviation management