QA Specialist / QA Specialistess

Join Our Team in Bern

In Bern, we're not just expanding—we're reaching a major milestone by launching a new production site and introducing innovative ways of working. This reflects what it means to be a Persistent Pioneer in our BN DNA—bringing a pioneering spirit to everything we do. Whether you're an experienced professional, transitioning from academia, or coming from a related industry, you'll have the unique opportunity to influence how we work and grow.

Boost Our Team

In this key role, you will help ensure high-quality standards and contribute to the delivery of safe and effective pharmaceutical products. You will oversee and provide leadership for all Computer System Validation (CSV) activities, as well as Qualification and Validation (QV) processes at the site. Your mission will involve ensuring compliance with regulatory requirements, internal quality policies, and industry best practices, thus supporting the development and manufacture of safe, effective, and compliant products.

Your Tasks

• Develop, review, and approve CSV and QV strategies, plans, protocols, and reports for new and existing facilities, utilities, equipment, and computerized systems.
• Partner with cross-functional teams such as Engineering, Manufacturing, IT, and other Quality services to ensure compliance and timely project execution.
• Participate in audits and inspections related to CSV and QV, ensuring readiness and robust documentation.
• Drive a culture of quality, compliance, and continuous improvement within CSV and QV activities, mentoring team members and stakeholders as needed.
• Support changes and corrections related to CSV and QV.
• Act as a subject matter expert (SME) for relevant regulations and guidelines, including EU GMP (EudraLex Volume 4, Annex 11 and 15) and FDA 21 CFR Part 11.

About You

• University degree in engineering, life sciences, computer science, or a related field.
• Minimum of 5 years of experience in CSV and ideally QV within the pharmaceutical, biotechnology, or related regulated industry; experience in QA is a plus.
• Demonstrated capability to drive and coordinate complex validation projects in a cross-functional environment with multiple stakeholders.
• In-depth knowledge of cGMP, GAMP, FDA, EMA, and other relevant regulations and guidelines.
• Strong technical writing, problem-solving, and project management skills.
• Excellent written and spoken English skills; German is an advantage, combined with strong interpersonal and communication abilities.

Why Join Bavarian Nordic?

We provide an opportunity to be part of an international company that boasts exceptional technology and a determined team. Join us if you share our enthusiasm and have a desire to create an impact. You can expect a vibrant and adaptable work environment that supports the growth of your personal and professional skills.

Ready to Join Us?

If this sounds like the next step in your career, we would love to hear from you. Apply online using the form below. Please note that only applications matching the job profile will be considered.

About Bavarian Nordic

Bavarian Nordic is a global vaccine company with a mission to improve health and save lives through innovative vaccines. We are a preferred supplier of mpox and smallpox vaccines to governments to enhance public health preparedness and boast a leading portfolio of travel vaccines. Headquartered in Denmark, we have manufacturing, research, and sales offices across Europe and North America.

Bavarian Nordic is an Equal Opportunity Employer. All qualified applications will receive consideration for employment and will not be discriminated against based on race, color, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

For more information, visit www.bavarian-nordic.com.