Become part of a vital chain and contribute to our common goal of making people’s lives better. Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines sourced from human plasma and human cell lines. We are a privately-owned company, where the warmth of family meets the scale of a global organisation. 

Octapharma AB is located in northwestern Kungsholmen in Stockholm and has approximately 1,100 employees. 

Join us in shaping our vision to provide new health solutions advancing human life. 

Your main tasks and responsibilities 

• Develop towards becoming a Subject Matter Expert (SME) in microbiology and aseptic operations, supporting commercial manufacturing  
• Lead and contribute to microbiological deviation investigations, including root cause analysis and development of effective CAPAs 
• Actively participate in crossfunctional assignments and strategic quality improvement projects 
• Participate in internal and external inspections, and manage followup activities and documentation 
• Continuously build deep expertise in sterility assurance as part of your development journey within the Early Career Program 

 
 
Your expertise and ideal skill set 

• Recent university graduate within natural sciences, biotechnology, microbiology or similar 
• Up to 3 years of relevant work experience (excluding internships) ideally including exposure to quality assurance, or pharmaceutical production environments 
• Strong interest in developing into a sterility assurance expert/SME within a global biopharmaceutical company 
• Knowledge of GMP and interest in aseptic pharmaceutical manufacturing  
• Structured, analytical and confident in advanced data handling and digital systems 
• Willingness to relocate internationally for short-term rotations as part of the Early Career Program 
• Fluency in Swedish and English (German or French is a merit) 
   
   

Your department - where you make an impact  

• You will be part of Quality in Operations Sterility Assurance, within the Quality Unit, responsible for ensuring aseptic status of our facilities and our products  
• The department ensures compliance with regulatory requirements and secures robust sterility assurance systems across manufacturing 
• You will join a team of 16 dedicated colleagues and report directly to the Head of Sterility Assurance  
• As part of your development track, you will collaborate closely with production, QA, QC and global functions to build broad, hands‑on expertise 

Thrive with us 

• You save lives – We manufacture lifesaving medicines every day.
• Benefits – Bonus program, benefits portal, onsite naprapath and more.
• Familyoriented culture – Longterm focus on people and relationships.
• Bistro Bryggeriet – Homecooked meals, inhouse bakery and café.
• Competence development – Courses, trainee programs and digital learning solutions.

It´s in our blood 

 
We live diversity and stand for equal opportunities as an employer! We therefore look forward to receiving your application - regardless of age, gender, origin, sexual orientation, and religion.  

The Recruitment Process 

• Our recruitment process includes occupational psychological assessments, interviews, and reference checks. For the two final candidates, participation in an Assessment Center in Lachen, Switzerland, on June 9–10 is mandatory. All related travel expenses will be covered by Octapharma.
• For the final candidate, alcohol and drug testing will be carried out by our occupational health provider. 
• The application deadline is 2026-03-24

Would You Like to Get to Know Us Better?  

 
Read more about Unit and follow our day‑to‑day updates on LinkedIn.

For this position, we have chosen to manage the recruitment process internally and therefore kindly ask recruitment agencies to refrain from contacting us.