Process Engineer Pharmaceutical Manufacturing 17251

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 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