Job Description

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