Arbetsbeskrivning

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 looking for a Process Engineer with experience in the pharmaceutical industry

What You Will Work On

• Validate production equipment, including vial filling machines
• Handle deviations and ensure proper documentation and resolution
• Manage and execute change control (CC) activities
• Define technical requirements for production equipment
• Support troubleshooting and resolve technical issues in production
• Drive continuous improvement initiatives within manufacturing
• Collaborate with cross-functional teams in a GMP-regulated environment
• Ensure production processes meet quality and compliance standards

What You Bring

• University degree in engineering or a relevant scientific field
• Experience in aseptic manufacturing and filling equipment
• Experience working within pharmaceutical production (GMP environment)
• Experience as a Process Engineer or Validation Engineer
• Ability to work independently and manage technical responsibilities
• Strong problem-solving skills with a hands-on approach
• Flexibility and ability to adapt to changing project conditions
• Fluent in Swedish and English, both written and spoken
• Willingness to work evenings and weekends as part of a rotation