On behalf of a small but leading biotechnology company with services to support all stages of biologics development, I am currently looking for a QA Associate. In this role you will be part of a small, but growing international team and will be providing QA support to the European operations. The company will also support your career development.
Your tasks as a QA Associate are the following:
The employee will also be responsible for the archiving function and assisting in document management such as activities which include tracking and maintaining standard operating procedures/forms, training records and other internal records
Assist with QA SOPs and provide regulatory input for other department SOPs and company policies
Support regulatory and sponsor audits
Working in organizing and directing a cross-functional team to ensure compliance with applicable regulations for all compliance activities undertaken
Requires a degree in biology, chemistry or other scientific or related field
1-3 years of experience in pharmaceutical / biotechnology / CRO preclinical / clinical quality assurance operations
Exposed to knowledge of FDA GxP regulations and industry standards as they apply to the life sciences and pharmaceutical industries
Ability to work in fast paced environment where multiple projects are in process and must be completed in a timely manner
This employee will work independently with limited supervision.
Excellent oral and written communication skills are essential. Must be fluent in German and English.
Should you be interested in this opportunity then do not hesitate to send me your CV to . You can also reach me on for more information.
Please note that our client and not able to sponsor visas, therefore we are only able to consider applications from candidates who are citizens of the European Union or have the legal right to work in Germany.