Group Senior Analytical Specialist (m/f/d) - QC Method Compliance - Part Time - Temporary
Wien, AT
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 1700 employees, the Octapharma site in Vienna is the largest production site, and successful research and development location.
In this position, you will act as Data Manager and supporting Subject Matter Expert (SME) for Analytical Method Validation and Method Transfer activities.
Join us in shaping our vision to provide new health solutions advancing human life.
Your main tasks and responsibilities
- Support analytical method validation, method transfer and method comparison activities in collaboration with SMEs
- Coordinate validation and transfer activities including planning, documentation, data evaluation and reporting according to GMP requirements
- Prepare, review and maintain validation documentation, Master Methods of Analysis and product specifications
- Support troubleshooting and investigation activities together with global QC stakeholders
- Manage and maintain QC-related databases and corporate document management systems (e.g. Veeva)
- Coordinate reference material calibration activities including documentation and stability verification
Your expertise and ideal skill set
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Degree in Life Sciences, Chemistry, Pharmacy or a related field
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Experience in Quality Control within the pharmaceutical industry
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Good understanding of GMP requirements and analytical data evaluation
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Strong organizational, communication and project management skills
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Confident handling of MS Office and data/documentation systems
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Fluent English skills
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.