Process Engineer Pharmaceutical Manufacturing 17251
About this role
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