CareerPlan

Compliance Manager (m/w/d) 1-Jahresvertrag

Laupheim, BADEN_WUERTTEMBERGFull-time2026-10-30 → 2026-11-05

Core

Ensuring manufacturing compliance with legal and regulatory requirements for biopharmaceutical production.

Role type

Manufacturing Compliance Manager

Builds

Biopharmaceutical products

Domain

Biopharmaceuticals / CDMO

Required skills

GMP compliance, Deviation Management, Root Cause Analysis, CAPA implementation, GMP documentation, Production audit support, Process improvement

Preferred skills

Biopharmaceutical active substance production knowledge, MS Office

Technologies

GMP, MS Office

Responsibilities

Ensure manufacturing compliance with legal and regulatory requirements; Handle deviations, OOS, and OOT results; Conduct root cause analyses; Establish CAPAs; Create and review GMP documents; Present deviations and CAPAs during audits; Organize production rounds for hygiene and contamination control.