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 from the pharmaceutical industry and strong technical expertise within aseptic manufacturing environments.

What You Will Work On

• Support validation and qualification of manufacturing equipment
• Define technical requirements and create URS documentation
• Handle deviations and support investigation activities
• Participate in CAPA processes and corrective action initiatives
• Manage and support Change Control (CC) activities
• Troubleshoot and resolve technical issues within production environments
• Support continuous improvement and operational optimization initiatives
• Collaborate with production, quality, engineering, and validation teams
• Ensure compliance with GMP requirements and manufacturing standards
• Contribute to stable and efficient pharmaceutical production operations

What You Bring

• University degree within Engineering, Science, or a related technical field
• Experience working within aseptic manufacturing environments
• Experience from pharmaceutical manufacturing and GMP-regulated operations
• Experience working as a Validation Engineer and/or Process Engineer
• Strong understanding of qualification and validation processes
• Ability to work independently in operational production environments
• Strong problem-solving capabilities with a hands-on mindset
• Flexible and adaptable approach in changing project environments
• Ability to communicate effectively in both Swedish and English, spoken and written
• Comfortable working evenings and weekends when required