Manager, QC Chemistry

Can you lead and develop a growing team of dedicated, empowered Validation Scientists and Subject Matter Experts?

As (Senior) Manager of QC Chemistry Scientists, your main focus is to empower team members to secure Customer deliverables, lead and develop your growing unit in accordance with our Company Core Values of Teamwork, Quality, Trust, Knowledge, Ingenuity and Accountability and to live up to GMP regulations.

Regulatory Affairs Specialist

Want to drive compliance across global markets and contribute to a mission of improving healthcare access worldwide?

Join us as a Regulatory Affairs Specialist in our new office in Copenhagen and play a key role in ensuring our medical devices meet regulatory requirements in over 85 markets.

Business Partner, CMC Biologics

Are you curious about the inner workings of a leadership team in the pharmaceutical industry and passionate about business processes and science? Do you thrive in a global setting and enjoy collaborating with multiple stakeholders in a fast-paced organization?

As a key member of the leadership team, you will plan, prepare, and participate in organizational and leadership initiatives, meetings, and related activities to support the strategic development of the area.

Senior Manager GQA Corporate Audits

Are you meticulous, curious, and interested in joining a team where your high integrity is trusted and valued?

If you have a strong background in pharmaceutical manufacturing and quality assurance, we invite you to join Ferring Pharmaceuticals as a Qualified Person (QP).

In this business-critical function, you will support our R&D CMC teams in development projects, delivering high-quality Investigational Medicinal Products to clinical trials across the world.

Director - Analytical Development, Methods & Characterisation

Do you find great professional fulfillment in empowering individuals to excel in their roles, and do you have experience managing a team of highly skilled scientists?

As Director of Analytical Development, Methods, and Characterization, you are encouraged to use a coaching leadership style to strategically strengthen the area of analytical method development, validation, and chemical characterization in the Ferring CMC organization.

Nyuddannet naturvidenskabelig akademiker til QC hos Xellia Pharmaceuticals

Drømmer du om at bringe din viden og nysgerrighed i spil i et medicinalfirma, hvor du kan videreudvikle dig?

Som Academic i QC-Support vil du både supportere kemiske og mikrobiologiske laboratorier, og du vil indgå i et team, der går op i sparring og løbende forbedringer. Du vil som Academic varetage både rutine- og forbedringsopgaver.

Senior Medicinal Chemist

We are seeking a highly motivated and ambitious senior medicinal chemist to help advance our small molecule drug discovery programs toward the clinic.

The successful candidate will be part of an entrepreneurial medicinal chemistry team in an expanding company.

They will partner with both internal and external medicinal chemistry teams to generate innovative solutions to synthetic and medicinal chemistry challenges within the context of small molecule drug discovery projects.

Cleaning Validation Specialist - bidrag til strategiske løsninger i vores farmaceutiske produktion

Er du klar til at sætte kursen for fremtidens cleaning validations i en global medicinalvirksomhed?

Her bliver du en af de centrale eksperter, der udvikler strategiske løsninger, som understøtter en løbende optimering og udvikling af både vores produktion og daglige drift.

Som en mindre virksomhed er vi gode til at give plads til den enkelte. Opsøger du udvikling, viden eller mere ansvar, så får du sjældent nej, og det giver dig mulighed for at dykke ned i dit område.

Clinical Pharmacology Scientist

We are committed to delivering life-transforming therapies for people living with neuromuscular diseases.

You will play a key role in the clinical development of our innovative drug candidates, from early development phase through late-phase clinical trials ensuring data-driven decision-making to optimize patient outcomes.

Be part of a team dedicated to improving lives through innovative therapies and flexible work options. On-site in Denmark. or remote work (US/Europe).

QA Academic, Corporate Product Quality Assurance Biologics

Do you possess an analytical and data-oriented mindset? Are you motivated by problem-solving and finding new solutions to the way we work with skilled colleagues?

The team consists of 4 employees (3 academics and 1 technician) who are responsible for all commercial QA-related activities in connection with oversight of Lundbeck’s biological production at our CMO’s, as well as review and release to market for these products.

Processansvarlig specialist til produktion af antibiotika

Er du klar til at få ansvaret for vores aseptiske produktionsanlæg, så vi kan levere antibiotika til hele verden?

Afdelingen producerer non-sterile og sterile pulverprodukter og inkluderer blandt andet processer som opløsning, frysetørring og pulverhåndtering.

I sådan et miljø får du en dagligdag med en bred kontaktflade, når du hjælper med at udbedre udstyrsfejl, sikrer kontinuerlig drift og vedligeholder vores procedurer.

Udstyrsansvarlig specialist til produktion af antibiotika

Er du klar til at få ansvaret for vores aseptiske produktionsanlæg, så vi kan levere antibiotika til hele verden?

Final Handling er bemandet på to skift alle dage, men vores processer kører døgnet rundt. I samarbejde med resten af teamet får du ansvaret for at udstyr drifter 24/7 uden længere stop og processer er optimerede.

Da dagligdagen er alsidig er der rig mulighed for at lære fra hinanden, både internt i teamet og i vores samarbejde med andre afdelinger.

Procesingeniør til pharma-projekter

Vil du arbejde med spændende og varierende projekter inden for proces design og kunne du tænke dig at blive del af et dygtigt tværfagligt team, hvor humøret og ambitionerne er tårnhøje? Kunne en 4-dages arbejdsuge friste?

I din hverdag kommer du bl.a. til at arbejde i projekter hos kunder såvel som fra vores kontor i Kalundborg. Du skal bl.a.

• designe, projektere, udføre kvalitetskontrol samt idriftsættelse af produktionssystemer
• bidrage med din procesindsigt og kendskab til anlægsdesign

QP-delegate for sterilproduktion

Kunne du tænke dig at blive en del af en spændende afdeling, der hver dag arbejder for at forbedre livskvaliteten for mennesker med psykiske sygdomme?

Som QP delegate vil du få en varieret og alsidig dagligdag med udfordrende opgaver.

Du vil primært være tilknyttet QA-teamet, der supporterer Lundbecks Sterilproduktion. På sigt vil der være mulighed for også at arbejde med QA-support til andre områder af Lundbecks produktion.