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

What You Will Work On

• Perform validation and qualification of manufacturing processes
• Handle deviations and support investigations in production
• Conduct risk assessments related to processes and quality
• Create and manage GMP-controlled documents
• Issue and approve technical documentation
• Ensure compliance with GMP standards and regulatory requirements
• Collaborate with cross-functional teams in production and quality

What You Bring

• Experience as a Process Engineer within pharmaceutical or similar regulated industry
• Strong knowledge of sterile manufacturing and aseptic processes
• Experience working in GMP-regulated environments
• Experience with validation, qualification, and deviation handling
• Ability to perform risk assessments and manage technical documentation
• Strong analytical and problem-solving skills
• Good communication and collaboration skills
• Fluent in English