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Group Senior Analytical Specialist (m/f/d) - QC Method Compliance - Part Time - Temporary

Octapharma Pharmazeutika Produktionsges.m.b.H -
Wien, W

Jetzt bewerben

Details zur Stelle

Vollzeit
vor 3 Tagen

Qualifikationen

Master

Vollständige Stellenbeschreibung

Stellen-ID: 63134
Standort: Wien, AT
Karrierestufe: Entry Level
Fachbereich: Quality
Beschäftigungstyp: Temporary employment

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.

This is a temporary part-time position (12 hours/week) covering a maternity leave, initially limited until June 30, 2028.

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

Degree in Life Sciences, Chemistry, Pharmacy or a related field
Experience in Quality Control within the pharmaceutical industry
Good understanding of GMP requirements and analytical data evaluation
Strong organizational, communication and project management skills
Confident handling of MS Office and data/documentation systems
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

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.

Jetzt bewerben

Erweiterte Suche

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