Vacant job

About the role

We are looking for an operator in pharmaceutical manufacturing for our production unit in Södertälje.

The role involves practical and operational work in our GMP-regulated facility. You will work according to established instructions, adhere to current quality requirements, and continuously document your work in production and batch documentation.

Your responsibilities include, but are not limited to:

• Working in cleanroom environments
• Sampling according to instructions
• Inventory management and material flow
• Preparation, filling, and handling of materials according to established procedures
• Documentation in production and batch records
• Cleaning and preparation of equipment and work surfaces

Production primarily takes place in cleanrooms, and the work schedule may involve two shifts. Evening work is required.

About you

To thrive and succeed in this role, we see that you are structured, responsible, and meticulous. You have a high awareness of quality, learn new tasks easily, and understand the importance of following instructions and documenting correctly.

We believe you have:

• Good ability to work systematically and carefully
• Quick learning ability and good problem-solving skills
• Strong quality sense and understanding of documentation requirements
• Ability to work independently and take personal responsibility
• Stress tolerance and ability to prioritize when necessary
• Good knowledge of Swedish and English

Previous experience in pharmaceutical manufacturing, GMP, cleanrooms, or other regulated manufacturing environments is advantageous, but not a requirement.

We place great emphasis on your personal qualities.

Training and introduction

The employment begins with an introduction and GMP training before access to production is granted. You will then receive training in our working methods, procedures, and production processes.