Job Description

An international life sciences environment is seeking a QA Consultant to support operational Drug Substance QA during a peak period. This hands‑on on‑site role focuses on batch record review and manufacturing support in a GMP setting.

Job Details

Location: Hillerød, Zealand Region
Category: Quality and Compliance
Salary: Apply for details
Country: Denmark
Employment: Contract
Worksite: On‑Site

Role

You will support the business in maintaining batch release timelines by working closely with manufacturing and technical teams in a live production environment.

Key Responsibilities

• Review and approve batch records both on the shop floor and within QA systems
• Support real‑time QA activities in a live manufacturing environment
• Act as QA partner to manufacturing and MSAT, resolving batch record queries
• Ensure GMP compliance while taking a pragmatic appro...