Computer System Validation Engineer (m/f/d) – Pharma Manufacturing

Overview

EFOR is a leading European consultancy specializing in technical and validation careers in the pharmaceutical and life sciences industry. We connect talented professionals with world-class projects in regulated sectors.

Job Description

Are you an experienced Computer System Validation (CSV) Engineer seeking to make an impact within the pharmaceutical production sector? We are recruiting two CSV Engineers for a long-term project in the Munich region.

Your Responsibilities

• Validate and qualify automated systems (CSV) in a regulated pharmaceutical manufacturing environment
• Manage and document all validation lifecycle activities according to GxP, GMP, and industry standards
• Apply your expertise working with PSC 7 (Siemens process control system) in production settings
• Collaborate closely with engineering, quality, and manufacturing teams
• Assist in audits, inspections, and continuous improvement initiatives for automation and data integrity

Your Profile

• Degree in Engineering, Information Technology, Life Sciences or related discipline
• Minimum 5 years (Intermediate) or 8 years (Senior) experience in Computer System Validation within the pharmaceutical sector
• Must-have: Hands-on experience with PSC 7 / PCS 7 (Siemens)
• Ideally, previous experience with filling lines, aseptic production, packaging, or similar pharmaceutical environments
• Strong command of English (project language); German proficiency is an asset
• Team-oriented, solution-driven, and willing to work in the Munich area (relocation/mobility support possible)

Interested? You can apply directly here or share your CV or share it by email to