Pharmaceutical Process Engineer 17681

Om jobbet

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