CareerPlan

Biologe (m/w/d)

Düsseldorf, NORDRHEIN_WESTFALENFull-time2026-10-06 → 2026-11-03
On-site

Core

Ensuring regulatory and quality compliance for engineering processes, documentation, and training within a biotech/pharma manufacturing environment.

Role type

Specialist Engineering Compliance (Quality/Regulatory)

Builds

Standard Operating Procedures (SOPs), training materials, and compliance documentation for vaccine production.

Domain

Biotechnology / Pharmaceutical Manufacturing

Deliverable

dashboards & analysis

Required skills

Technical writing, GMP knowledge, CMMS, Microsoft Office, regulatory compliance understanding

Preferred skills

Experience in pharmaceutical industry, stakeholder communication

Technologies

CMMS, Microsoft Office

Responsibilities

Create, review, and approve SOPs; Ensure adherence to quality and regulatory standards; Develop and maintain training materials; Conduct employee training; Optimize documentation and compliance processes