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Operators for Drug Product Manufacturing

Would you like to be part of an international pharmaceutical company in rapid growth, which offers good development opportunities and set shifts?

This project is in the early phase of establishment and in the beginning, you will help design and establish processes for the upcoming production.

Main tasks:

• Participate in running and validation of equipment on site
• Assist during installation of equipment on site and carry out qualification tests afterwards

Operations Data Coordinator for Drug Substance Production

The primary task within the position is to collaborate with various departments (e.g., automation, tech transfer, and manufacturing departments) to collect and translate information required for building efficient production campaigns and daily task schedules.

You will be part of a team with a great sense of humor and a high willingness to support where needed.

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.

Manufacturing Support Documentation Associate

Do you have a flair for compliance and can handle many stakeholders? Are you looking for a position where you can take on responsibility?

About the position:

• Create and maintain records and procedures by collecting information from stakeholders to supply manufacturing with compliant documents.
• Start-up events and support investigations by giving input as procedural SME.
• Support the change process by writing SME assessment to ensure procedural alignment. Perform timely closure of action items to ensure reliable execution of production.
• Continuously improve the department processes and support stakeholder improvement projects.

Research Analyst

Are you in the right job? Do you want a challenge out of the ordinary?

The Primary Research Analyst has the responsibility of identifying, developing, and maintaining a network of contacts and relationships in the pharmaceutical and biotech industry and organizations.

An academic background in pharmacy or in biotechnology is an advantage but not a necessity as extensive internal training will be provided.

Column Pack Operator

The work we do at FUJIFILM Diosynth Biotechnologies (FDB) has never been more important—and we are looking for talented candidates to join us. We’re growing our locations, our capabilities, our teams and looking for passionate, mission-driven people who want to make a real difference in people’s lives.

We are currently looking for candidates to work within Drug Substance Manufacturing (DSM) Support and become part of a newly established team, responsible for preparation, packing and qualification of chromatography columns.

Manufacturing Supporter

We are looking for a talented Manufacturing Supporter for the Drug Substance Production to join the DS Documentation and Support Department in Hillerød.

The work we do at FUJIFILM Diosynth Biotechnologies (FDB) has never been more important—and we are looking for talented candidates to join us.

You will be part of a team, consisting of 14 people, with a great sense of humor and a high willingness to support where needed.

Clinical Trial Manager til innovativt forskningsmiljø inden for hjertesygdomme og randomiserede studier

Er du en stærk analytiker med erfaring i at planlægge og udføre kliniske forsøg? Vil du være ansvarlig for at starte nye internationale kliniske forsøg op i Danmark sammen med vores samarbejdspartnere?

Kunne du tænke dig at arbejde med at gøre vores vision om kortere vej fra forskning til patientbehandling muligt?

Din opgave som Clinical Trial Manager vil være at lede implementering, udførelse og afslutning af kliniske forsøg i henhold til gældende studieprotokol og retningslinjer for Good Clinical Practice (GCP).

QA Assistant

Motiveres du af en stilling, hvor du har fokus på systemer og kvalitet? Og vil du arbejde med fremstilling af pakkematerialer til den farmaceutiske industri?

Du vil få daglig sparring med operatører, specialister og ingeniører i vores produktionsenhed i Horsens – som årligt producerer ca. 2,5 milliarder enheder.

Vi tilbyder en spændende stilling med mulighed for at sætte dit personlige præg på måden, tingene fremadrettet skal gøres på.

Business Developer with a background in Science

Do you want to be at the forefront of Targeted Radiopharmaceuticals and Molecular Imaging?

We are looking for a professional Business Developer with a background in life sciences and the ambition to contribute to further strengthening Minerva Imaging as the trusted partner for targeted radiopharmaceuticals and molecular imaging.

What truly matters is your passion for the advancement and know-how of our scientific studies and your ability to foster long-term relationships with our collaborators.

Manufacturing Associate - Operator

We are looking for process operators, preferably with experience from a similar pharmaceutical production company or similar regulated businesses OR a Life Sciences Graduate who have recently finalized their Bachelor or Master degree relevant for Biologics Manufacturing and are keen on starting their career in a manufacturing and international environment where things move fast.

We are hiring for attitude, so we are looking for people who have a lot of drive and proven interest with working under GMP and enjoy working with numbers, math and IT tools.

QA-assistent med GMP-erfaring

Vi søger vi en erfaren og selvstændig QA-assistent, der har lysten til at være en del af udviklingen af en nystartet state-of-the-art-bioethanol-produktionsvirksomhed.

Dine primære arbejdsopgaver vil være:

• Vedligeholdelse af QMS-system, instruktioner, vejledninger osv.
• Review af batchdokumentation.

Du tilbydes en attraktiv og konkurrencedygtig lønpakke med pension og sundhedsforsikring.

Senior Specialist Clinical Safety and Pharmacovigilance (CSPV)

At Bavarian Nordic, we aspire to save and improve lives by developing innovative vaccines that are designed to unlock the power of the immune system.

The global team consists of subject matter experts for vaccine safety who work either from our site or remotely in Denmark and globally. Together they constantly collect and assess data for the life cycle benefit risk management across our vaccines whether authorized or still in clinical development.

You would add your clinical safety and pharmacovigilance expertise as your depth knowledge of the PV legislation to the team.