QIAGEN is one of the world’s leading biotechnology companies. With our sample to insight solutions that unlock valuable molecular information from biological samples, QIAGEN helps to improve healthcare and safeguard our societies, enables the development of new medicines and paves the way for scientific breakthroughs.
Join the revolution – and see how you can make a difference
Specialist Regulatory Affairs
Job ID#: 9882
Location: Wroclaw (Breslau), Poland
Functional Area: Regulatory / Clinical / Medical Affairs
Employment Type: Regular Full-Time
Duration: unlimited
Position Description
- Provide support to the Global Regulatory Affairs Registration team for product registration and renewals.
- Coordinate Post Market Surveillance Activities for launched products.
- Support internal stakeholders with product registrations and maintenance activities, customer enquiries and provision of regulated documents as required.
- Maintain technical documentation for QIAGEN products to support inspection by Regulatory bodies.
- Oversight of data quality for the regulated products within the company databases.
Position Requirements
- Minimum scientific degree (or equivalent) in life sciences required.
- 1-2 years’ experience in a similar role within a regulated industry i.e. Pharmaceuticals, Medical Devices, (preferably in vitro diagnostics).
- Working knowledge of the European and other International regulations.
- Proficient with Microsoft Office and experience with SAP and Trackwise.
- Good command of English Language.
Personal Requirements
- Good interpersonal and communication skills.
- Ability to handle multiple projects simultaneously.
We offer
- Possibility to develop in an international company.
- Attractive office location in Sky Tower.
- Attractive benefits package.
- Language classes.
- Private medical care.
- Group Life Insurance.
- Friendly atmosphere.
- Happy Monday :)
