Senior Compliance Professional

Do you have broad experience with compliance-related matters within root cause investigations and systematic problem-solving in a pharmaceutical Engineering or Manufacturing organization?

We offer you a chance to work in a dynamic environment with excellent opportunities to develop your personal and professional skills. You will join a team dedicated to well-being and goal achievement, while also fostering an enjoyable and engaging work environment.

Senior Application Specialist

Are you experienced in the Supply Chain processes around D365 F&O, and are you motivated by working hands-on in a business-critical system within a growing Pharma Company?

Do you thrive on collaborating with process managers, superusers, business stakeholders, vendors, and other D365 colleagues?

Then you might be our new D365 F&O Application Specialist!

Environmental Professional

Har du lyst til og mod på at udvikle dig i en spændende virksomhed, eller er du bare er overbevist om, at din karriere i medicinalindustrien skal have en ekstra dimension? Kan du lide at arbejde med blandt andet GMP, forbedringer, aseptisk- og vaccineproduktion og kvalificering af udstyr?

Som vores nye miljøsupporter vil du blive involveret i den daglige drift, og vi vil sikre, at du får de rigtige kompetencer til at løse dine opgaver, så du nemt kan supportere vores vaccineproduktion med at håndtere dagligdags udfordringer i vaccineproduktionen

Manager – Global Governance for Maintenance and Metrology

We are looking for a dedicated Manager for our Global Maintenance and Metrology team who shares our passion, drive, and energy to make a difference.

Your main responsibilities:

• Manage the team of Engineers to support Maintenance and Metrology strategies
• Setting strategic direction for Metrology and Maintenance across Bavarian Nordic
• Project manager for the upgrade of current and new Metrology and Maintenance systems

Technician

Har du erfaring med teknisk arbejde inden for den farmaceutiske industri?

Du kommer til at være teknisk ansvarlig for vedligehold på utility-anlæg (damp, kedelcentral, vandanlæg, waste og køleanlæg).

Dine opgaver bliver bl.a. fejlfinding og udførelse af vedligehold på utility og forsyningsanlæg samt udarbejdelse af forebyggende vedligeholdelsesplaner (FMECA).

Director of External Manufacturing Commercial Operations

Are you an experienced leader looking for your next opportunity and have an interest in working with Contract Manufacturing Organizations?

You will be an important contributor in designing and shaping how we work with our portfolio of external manufacturers (CMO's).

The team and organization are relatively new, so you will have a significant impact on the way we work in the team as well as across the organization, to ensure that our products are manufactured on time and in the right quality.

EHS Specialist

As an EHS Specialist, you will work closely with the Biosafety Officer (BSO) to ensure compliance and safety throughout the production area. You will implement necessary safety measures, promote a culture of health and environmental responsibility, and act as the main contact for regulatory bodies and inspectors.

Furthermore, you will manage responses to bio-related incidents, minimizing impact and restoring operations promptly. Partnering with the BSO, you will address chemical, biological, general safety, and biosecurity risks, ensuring aligned health and safety policies.

Laborant QC Sampleflow

Har du laboratorieerfaring og kunne du tænke dig at tage det næste skridt i din karriere?

Du får ansvar for og stor medbestemmelse over dine opgaver så de fleste dage vil gå stærkt, og opgaverne bliver ofte andre end dem, du havde planlagt og forventet.

Du vil opleve en dynamisk og udfordrende hverdag i QC, med mange spændende opgaver og en åbenhed over for nye idéer.

QA Specialist for Environmental Support

In this role, you will join Bavarian Nordic's QA Organization as a QA Specialist tasked with establishing strong relationships with stakeholders, effectively communicating GxP requirements, and handling crucial Quality Events in the Quality Management System (QMS).

This is in the context of environmental monitoring, aseptic performance, and sterile & low bioburden processes in Drug Substance and Drug Product Production. Additionally, you will contribute to the ongoing improvement of QA processes to elevate overall quality standards.