Pharmaceutical Process Engineer - 17681

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

If this sounds interesting please send your CV at cv@veritaz.se

Pharmaceutical Process Engineer – 17681

Huy Tran

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Job Description

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