Summer Intern (m/f/d) - Corporate QC Method Validation - temporary

Job ID:  62180
Location: 

Wien, AT

Job Level:  Entry Level
Job Category:  Quality
Employment Type:  Temporary employment
Career Level: 

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.

 
This position is temporary from 01.07.2026 until 31.08.2026 (2 months) or from 01.08.2026 until 30.09.2026 (2 months) with 38 hours per week.


We look forward to receiving your application. Please upload the following application documents: cover letter stating your desired period of employment, CV, and your high school diploma or degree certificate and a current transcript of your academic achievements.

 

Your main tasks and responsibilities

 

  • This internship is designed to complement your training and give you an insight into the work and activities of a pharmaceutical production company
  • Supporting documentation & improvement within the department
  • Diverse administrative tasks within the cQC Method Validation department 

 

Your expertise and ideal skill set

 

  • Students with a scientific background
  • Practical work experience desirable (internships, etc.)
  • Fluency in English
  • Interest in analytics
  • Valid vaccination protection against hepatitis A and hepatitis B
  • Valid residence and work permit for Austria
  • Good skills in Microsoft Office (Word, Excel, Power Point)
  • Sense of responsibility, flexibility and ability to work in a team
  • Organizational talent, multi-tasking and accurate way of working

 

Your department - where you make an impact  

 

  • We, the Corporate Quality department, are responsible for the development of policies and procedures for all CQ Plasma activities based on current applicable regulations to ensure a standardized approach throughout the organization.
  • We are divided into CQ Plasma, CQ Control, Corp. Stability Studies, Corp. QC Method Validation and Corp. QC Incoming Goods.



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 2,010.75 (with high school diploma and/or over 18 years of age) based on 38 hours per week (full-time).

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. 

Mrs. Eveline Kastner (MON – THU)
Octapharma Pharmazeutika Produktionsges.m.b.H. 
Oberlaaer Straße 235, 1100 Wien 
T: +43 664 88 14 2750 



Want to find out more about us? 

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

 

About Octapharma

Octapharma is one of the largest human protein manufacturers in the world, developing and producing human proteins from human plasma and human cell lines. We employ more than 11,000 people worldwide to support the treatment of patients in 120 countries with products across three therapeutic areas: Immunotherapy, Haematology and Critical Care. With seven R&D sites and five state-of-the-art manufacturing facilities in Austria, France, Germany, and Sweden, Octapharma also operates over 195 plasma donation centres across Europe and the US. With four decades of experience, we are committed to advancing patient care worldwide.