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.

Kvalitets- og udviklingsingeniør til en virksomhed der, med stort fokus på bæredygtighed, arbejder med genanvendelse af plastspild

Dit fokus bliver at sikre tilfredse kunder igennem en ensartet høj kvalitet i både virksomhedens produkter og services. Der skal være styr på tingene, og man hjælper hinanden. Derudover skal du varetage udviklingen af nye produkter i samarbejde med salg og produktion.

Lyder det som en udfordring for dig, og er du parat til det næste skridt i din karriere?

Account Manager for Clean Air applications

You will be responsible for a wide variety of tasks within sales and business development. Your daily work will involve extensive contact with customers, partners as well as internal departments going from quote to the delivery of goods and building/managing an international distribution network.

You will be part of a dedicated taskforce with the objective of accelerating the business development of our Catalytic Filtration and Catalytic Oxidation for VOC control solutions.

Senior Scientist, organic chemistry

Vipergen is an innovative biotech company dedicated to small molecule drug discovery using DNA-encoded chemical libraries.

We are currently looking for a highly skilled organic chemist who can join our dynamic team of molecular biologists and chemists. Your key responsibilities will include:

• Continued development of DNA-encoded libraries and support the synthesis thereof
• Analysis of complex screening data including reporting screening results to external partners

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.

PhD Scholarships in Piezoelectric Biopolymer Technology and Devices for Drug Delivery on Demand – DTU Health Tech

The aim of the PhD project is to explore and develop new piezoelectric biomaterials and technologies for controlled drug release in smart devices by the application of ultrasound.

Your overall focus will be on the design, realization, and test of devices such as smart pills or flexible MEMS transducers based on piezoelectric biopolymers such as chitosan and cellulose, the two most abundant biopolymers on earth. You will work with nearby colleagues and with academic, clinical, and industrial partners in Denmark as well as abroad.

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.

Laboratory Technician Trainee (Immunology)

You are expected to participate in lab routine tasks and in vitro validation assays. With guidance, you are capable of planning the daily work and execute with precision and speed while observing all safety regulations and protocols.

You will take ownership of the assignment and proactively propose solutions to the issues that arise. You are expected to carry multi-tasks and work independently after training.

Category Manager in Raw Materials Procurement

The department you will join is globally responsible for securing the raw materials for our existing productions in Denmark and USA as well as our upcoming productions related to our carbon emission reduction technologies.

You will:

• Drive category planning, management and sourcing strategies
• Have responsibility for supplier segmentation and global supply base within own categories
• Drive and negotiate strategic and partnership agreements within own categories

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.

QA Device Senior Manager

Currently, we are looking for a new QA Device Senior Manager, who has experience with providing QA support to Drug/Combination Products development projects (early phase to Commercial).

You will be a part of GMP QA, which is a dedicated QA team focusing on supporting product and device activities for development and commercial products. We are working as quality assurance partners in an international environment with companies and stakeholders to ensure continuous compliance using an up-to-date knowledge of external requirements.

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.

Quality Control Technician Pipeline, AGC Biologics

Are you interested in working with the latest equipment and technology? Do you have a background in process operations and experience with systems? Do you thrive in a dynamic, fast-paced environment? If so, AGC Biologics could be this right place for you!

You'll have the opportunity to work on a variety of tasks and challenges across different departments. We value teamwork and offer an informal working environment characterized by high energy and enthusiasm.

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.