Aseptic Process Specialist 16977

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

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