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.

With over 1600 employees, the Octapharma site in Vienna is the largest production site, and successful research and development location.

As a Group Expert Analytical Specialist, you will drive innovation and continuous improvement initiatives within Group Quality Control.

The position is temporary until April 30, 2028 due to maternity leave coverage.

Join us in shaping our vision of providing new health solutions advancing human life.  

Your main tasks and responsibilities 

• Develop and validate analytical test methods in compliance with GMP and official pharmaceutical standards 
• Act as Global Subject Matter Expert for Method Validation & Transfer, including protocol review, risk assessment, troubleshooting, data evaluation, cross-site coordination, and reporting
• Establish and maintain Group-wide analytical standards, controls, and reference systems
• Regular exchange and communication with the test laboratory
• Serve as a key contact for Global QC-related projects across departments
• Perform cross-site comparisons of potency parameters

Your expertise and ideal skill set 

• University degree (MSc, PhD, or equivalent) in natural sciences
• Proven experience working in GMP-regulated environments as well as in statistical data analysis
• In-depth knowledge of Analytical Chemistry, statistics, and GMP regulations
• Advanced MS Office skills, especially Excel
• Excellent English communication skills (oral and written), combined with strong interpersonal and presentation skills
• Strong problem-solving and time-management skills, with the ability to multitask

Your department - where you make an impact  

• We, the Group Quality department, provides strategic alignment across local Quality Control departments, analytical method validation, and stability studies, ensuring efficient processes and regulatory compliance.

Thrive with us

• Company restaurant & meal subsidy 
• Training & further education 
• Health promotion 
• Parking spaces and good public transport connections  
• Company and team events 
  
  

Enjoy these attractive benefits! You can find all offers here: Benefits

The minimum gross salary according to the collective agreement (chemical industry) is EUR 4,270.14 based on 38 hours per week (full-time). As we strive to offer a salary that reflects your individual profile and qualifications, there is a willingness to pay above the minimum salary.  

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.  

Do you have any questions? Then get in touch with your contact person. 

Larissa Amling 

Octapharma Pharmazeutika Produktionsges.m.b.H. 

Oberlaaer Straße 235, 1100 Wien 

T: +43 664 789 53 728

Want to find out more about us? 

 
Visit our website Octapharma Career and follow us daily on LinkedIn.