GCLP Administrator (m/f/d) Immunomonitoring
Are you ready to see our vaccine pipeline come to life? Are you organized and a very structured-working person? Would you like to become the go-to-person in the Immunomonitoring team for administrative tasks and documentation management? Would you like to work in a regulated environment, and do you enjoy maintaining quality standards? Then we would like to meet you! We are looking for a GCLP administrator/assistant (m/f/d) to support our Immunomonitoring department.
Strengthen our Immunomonitoring Department
We are in the process of building a highly motivated and skilled team that will develop immunological assays and utilize them to evaluate the immunogenicity of Bavarian Nordic’s new innovative vaccines in clinical trials.
As GCLP Administrator (m/f/d) in the Immunomonitoring group, you will be part of the successful development of these vaccines. You will support the team in the maintenance and improvement of the GCLP quality standard. You will be involved in the preparation and successful performance of audits and inspections by our quality assurance colleagues and external agencies regarding administrative and documentation tasks.

Your tasks:

• Team assistant supporting documentation and organisation of the department
• Quality representative of the department
• Ensuring regular maintenance of GxP equipment
• Preparation and administration of equipment logbooks
• Preparation and maintenance of GxP relevant lists, records and files (e.g. equipment list, critical material list, etc.)
• Receival, logging and shipment of clinical samples, including documentation and inventory using an electronic sample management system
• Receival, logging and management of GxP media, reagents and equipment
• Maintenance and improvement of GCLP

About you

Your qualifications

• Biological technician qualifications e.g. MTA, BTA, CTA, PTA or equivalent, or another qualification with GxP experience
• GxP knowledge
• Team player who enjoys supporting her/his colleagues
• A high level of responsibility and an independent and reliable way of working
• Good knowledge of and experience with MS-Office (Excel, Word, databanks)
• Good English communication skills

We offer

• An exciting position in Immunomonitoring
• Be part of a newly formed talented, international team from the start.
• The chance of professional development through our dynamic company structure.
• Broadening your experience in an internationally operating biopharmaceutical company.

Caught your interest?
If you are interested in the position, we look forward to receiving your complete application in English via our online application system. The application should include CV, cover letter, and copies of your academic or vocational education degree certificate. Please upload documents in PDF format only.
We kindly request that headhunters or recruitment agencies refrain from contacting us regarding this position.
Founded in 1994, we have +30 years of experience developing life-saving vaccines. We are a global leader in smallpox and mpox vaccines. Our commercial product portfolio contains market-leading vaccines against rabies, tick-borne encephalitis, cholera, typhoid, and Ebola. We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe and North America. Our values – our Bavarian Nordic DNA, as we like to call it – are what guide our actions every day. We act as persistent pioneers, embrace change, value being boosted by the team, and believe in protecting lives every day. If that is also a part of your DNA, we invite you to join us in Bavarian Nordic! Bavarian Nordic is an Equal Opportunity Employer.
www.bavarian-nordic.com

• Team assistant supporting documentation and organisation of the department
• Quality representative of the department
• Ensuring regular maintenance of GxP equipment
• Preparation and administration of equipment logbooks
• Preparation and maintenance of GxP relevant lists, records and files (e.g. equipment list, critical material list, etc.)
• Receival, logging and shipment of clinical samples, including documentation and inventory using an electronic sample management system
• Receival, logging and management of GxP media, reagents and equipment
• Maintenance and improvement of GCL