Process & Equipment Validation Specialist 17859

Publiceringsdatum: 2026-05-24

Letar du efter möjligheter att arbeta inom yrken med teknisk inriktning? En möjlighet har öppnat upp för dig att börja arbeta som processingenjör, maskin hos Veritaz AB. Veritaz AB söker en medarbetare på heltid som vill arbeta 6 månader – upp till 12 månader. Kan det vara du?

Platsen där jobbet finns ledigt är i ospecificerad arbetsort. Veritaz AB behöver fler anställda som stödjer arbetet inom processingenjör, maskin. Kolla in deras lediga tjänst för att se om du har vad som krävs. Här är chansen att bli en del av Veritaz AB och jobba som processingenjör, maskin! Ansök senast tisdag den tjugotredje juni 2026.

Jobbannons

Veritaz is a leading IT staffing solutions provider in Sweden, committed to advancing individual careers and aiding employers in ensuring the perfect talent fit. With a proven track record of successful partnerships with top companies, we have rapidly grown our presence in the USA, Europe, and Sweden as a dependable and trusted resource within the IT industry.

Assignment Description

We are currently looking for a Process Engineer / Validation Engineer

What You Will Work On

• Develop test protocols and validation documentation for production processes
• Plan, coordinate, and execute validation and qualification activities
• Support commissioning and readiness of new production lines
• Perform process and equipment qualification activities
• Execute testing and verification in production and cleanroom environments
• Collaborate closely with operators, production teams, and technical stakeholders
• Develop and improve validation strategies and execution methods
• Support transition from project phases into commercial operation
• Contribute to process optimization and operational stability
• Ensure compliance with regulatory and quality requirements
• Participate in troubleshooting and continuous process improvements
• Support documentation and knowledge transfer activities

What You Bring

• Master's degree in Chemical Engineering, Biotechnology, or related field
• Experience as a Process Engineer and/or Validation Engineer within life sciences or production environments
• Experience working in GMP-regulated pharmaceutical manufacturing
• Experience operating in cleanroom and aseptic production environments
• Hands-on experience with qualification and validation activities (IQ/OQ/PQ)
• Strong ability to develop and write test and validation protocols
• Understanding of process equipment and production systems
• Experience working with control systems, tanks, freeze-drying processes, and oil-based processes
• Experience from industrial production lines and operational environments
• Knowledge of equipment and process qualification
• Understanding of project lifecycle phases including construction, qualification, and commercial operation
• Experience collaborating across technical and operational teams
• Structured and quality-focused approach to execution and documentation