Research Analyst

Would you like to become an expert on worldwide trends in the pharmaceutical and biotechnological industries?

Together with your colleagues, you will be responsible for ensuring that scope and objectives are met throughout the entire duration of the project and that all client requests are handled in a timely, accurate and unbiased manner.

You will experience great freedom to organize your own tasks and you will get the opportunity to contribute to the further development of our processes and key areas of expertise.

Continuous Improvement Partner for Drug Substance Manufacturing

This role will support the Leaders and alle the employees in their quest of developing the business towards operational excellence and working cross-functionally to boost and create a people focused improvement culture within the entire organisation.

Your primary tasks will include but not be limited to:

• Develop and sustain CI systems and tools.
• Coach on ideal behaviour that drives a proactive improvement culture.

(Senior) Medical Director (GI)

Are you an experienced in Medical Affairs with international experience and desire responsibility for a broad range of tasks? And are you interested in taking your medical affairs career to the next level by being exposed to and providing input to our research and development teams?

Your job responsibilities will include:

• Designing and managing the implementation of the medical affairs plan
• Cross-functional collaboration within R&D and other internal functions

Supplier Quality Engineer

Agilent provides life science, diagnostic, and applied market laboratories worldwide with instruments, services, consumables, applications, and expertise.

Your main responsibilities will include ensuring compliance with various regulations and standards, leading supplier quality compliance projects, developing partner quality agreements, managing high visibility SCARs, and conducting key supplier audits.

Lead Auditor - Senior Quality Compliance Specialist

Are you passionate about GMP auditing and quality while being eager to travel world wide to audit our suppliers and partners?

In this position, you will take the role as Lead Auditor in our dedicated team of auditors and highly skilled Quality Specialists ensuring compliance of our portfolio of Pharmaceutical Contract Manufactures by auditing against the EU GMP EudraLex Volume 4 regulation.

Manufacturing Technician Pipeline AGC Biologics

Join our production team, which consists of five production lines that manufacture preclinical, clinical, and commercial products for a diverse range of clients.

As a technician, you will be involved in planning and executing different steps in the production process, including protein purification and equipment setup.

It would be an advantage having 1+ years of experience in the biopharmaceutical or related industry, preferably in a cGMP environment.

Project Manager - CAPEX projects - EMEA

The position should be based at one of our Ingredients manufacturing sites in the EMEA region. There will be flexibility for remote work.

Responsibilities/description:

• Coordinates with Project Sponsor and Divisional Engineering Director to develop Business Objectives Letter.
• Leads and provides input into developing the project objectives.

Scientist Pipeline AGC Biologics

Are you passionate about ensuring quality in manufacturing processes? Do you have a scientific background and experience in Quality Assurance or Manufacturing? If so, we have an exciting opportunity for you!

You will be involved in:

• Upstream Processing: Cultivation of cells, media preparation, and bioreactor operation.
• Downstream Processing: Protein purification, filtration, and chromatography.
• Solution Preparation: Buffer preparation, media and solution mixing, and sterilization.

Pharmacovigilance Specialist

You will help our customers succeed in creating and/or maintaining a high-quality pharmacovigilance quality system.

Your tasks will include:

• all tasks related to pharmacovigilance work (processing of side effect reports, local monitoring of medical literature, monitoring of pharmacovigilance legislation, tasks related to signal detection, managing contacts with authorities, reconciliations, quality assurance tasks, tasks related to risk minimization)
• planning trainings and preparing training materials
• monitoring compliance with pharmacovigilance agreements

Regulatorisk medarbejder med kommerciel indsigt til spændende stilling med udviklingsmuligheder (genopslag)

Har du en stærk kombination af regulatorisk viden og kommerciel forståelse?

Pharma Nord søger en engageret og ambitiøs medarbejder til vores regulatoriske afdeling i Vojens. Vi søger en profil, som kan navigere lovgivningen inden for kosttilskud og som er resultatorienteret.

Som medarbejder i vores regulatoriske afdeling får du en vigtig rolle i at drive og udvikle vores compliance og forretningsudvikling. Du vil arbejde på tværs af organisationen for at sikre, at vi overholder alle relevante love og regler, samtidig med at du bidrager til opfyldelsen af vores kommercielle mål.

Process Engineer, Enzyme Recovery, Novonesis, Kalundborg

Are you looking for new challenges in a fast-paced environment where no two days are the same?

You will be part of a team of dedicated and skilled engineers and technicians with four main responsibilities:

• Process and product responsibility including daily supervision and optimization to meet business targets for quality, economy and regulatory requirements
• Optimization activities including identifying and driving technology projects to further improve our production processes and secure future capacity

Research Specialist

On behalf of our client Novo Nordisk, Moment, is looking for a full time Research Specialist to be part of a team which support the projects about Translational activities.

You and your team's key responsibility is to ensure governance and high-quality management of human biosamples and data across the research organization, by guaranteeing all legal documentation is in place.

Erfarne steriloperatører

Har du en passion for farmaceutisk produktion og drømmer om at spille en vigtig rolle i kvalitetssikringen af vacciner? Og har du erfaring som procesoperatør, industrioperatør, laborant eller farmakonom, så har vi måske det helt perfekte job til dig.

Du har praktisk erfaring med GMP, kvalitetskontrol og/eller kvalitetsstyring fra produktionslignende miljøer samt kendskab til sterilproduktion og aseptisk arbejde. Vi tilbyder spændende arbejdsopgaver i en international anerkendt virksomhed med danske rødder.

Sales Account Manager – Molecular, Biology & Research Solutions

Agilent is a global leader in laboratory and clinical technologies, we are passionate about bringing great science to life.

As a Sales Account Manager you will be responsible for the success of our Molecular, Biology & Research (MBR) solutions (including genomics, pathology, cell instrumentation, reagents, services and software) across Denmark.

As an integral member of the field sales team, you will use your excellent technical sales track record to focus on acquiring new customers, while retaining and growing the existing installed base of customers.

Scientific Senior Consultant

Vil du være en del af Helix Lab-teamet, og dermed være med til at udvikle et stærkt forsknings- og uddannelsescenter?

Din primære opgave vil være at sikre videnskabelig og teknisk ekspertise og kvalitet i Helix Labs laboratorier og projekter, samt at udvikle den videnskabelige projekt-pipeline baseret på industriens styrker og behov for digitalisering, automatisering og bæredygtig produktionen.

Compliance Operation Lead

Are you experienced with regulatory requirements for medical devices?

In this role, you will be responsible for supporting compliance with Agilent’s QMS and external requirements.

You will also be responsible for driving initiatives to ensure continuous improvements of our processes as well as collaborating with international colleagues to achieve company goals.