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Clinical Trial Assistant

Are you looking for the possibility to unfold your competences within clinical operations even further? Do you thrive in an innovative environment working alongside dedicated clinical research professionals? Are you a self-driven team player, who enjoys a varied and influential day at work?

Pharmacosmos A/S is a progressive and innovative pharmaceutical company with headquarters in Holbæk, Denmark. We are on an exciting journey of global growth inventing new and innovative treatments, and right now we are expanding our team with a Clinical Trial Assistant.

IT-arkitekt

Vil du være en del af et inspirerende velfungerende team med høje ambitioner for VIAs digitale udvikling og har du evner og lyst til at sætte dit præg på VIAs digitale arkitektur?

Du får i stillingen et stort selvstændigt ansvarsområde, hvor du kan udfordre dig selv og udvikle dine færdigheder.

Som it-arkitekt medvirker du til at skabe sammenhæng i VIAs digitale miljø og binde it og forretning sammen, hvad enten det er i forbindelse med nyanskaffelser, udvikling, videreudvikling eller dokumentation af eksisterende digitale processer og systemer.

QA Specialist

We are seeking a competent new colleague to join our QA team in a dynamic and growing company.

You will be part of our highly dedicated team consisting of 5 colleagues working with a broad range of QA tasks such as batch review, processing of complaints, deviations and change requests as well as validation and ad hoc projects.

Løsningsarkitekt til spændende og samfundsvigtigt it-projekt

Vil du være med fra begyndelsen i et stort it-projekt med høj samfundsrelevans? Vil du være med til at modernisere systemunderstøttelsen af vores sagsbehandling, så skatteyderne også i fremtiden oplever en effektiv og korrekt sagsbehandling, når det drejer sig om skat og moms?

Du vil naturligvis få et grundigt introduktions- og oplæringsforløb for at kunne arbejde selvstændigt med opgaverne.

Vi tilbyder gode arbejdsforhold og stor fleksibilitet i en ofte travl hverdag.

Regulatory Affairs & QA Lead

Har du lyst til at blive en del af en spændende arbejdsplads, som opererer globalt med nogle af markedets bedste produkter?

Som vores Regulatory Affairs & QA Lead bliver du en del af et velfungerende team med 5 engagerede kolleger, der hver dag arbejder målrettet og brænder for deres arbejde.

Der kan være mange indgangsvinkler til jobbet men du skal have erfaring med medicinsk udstyr, være omhyggelig, energisk og brænde for det regulatoriske arbejde.

Student Assistant in QA for Automatization Project

Would you like to be part of an exciting automatization project within Quality Assurance and interact with dedicated professionals from different backgrounds?

Are you ready to apply your IT skills to a company project? Would you like to develop yourself as a professional within the Pharma industry?

Then, you may be our new colleague within the Global Quality organization.

Senior Test Engineer

Join GE HealthCare to help perform transducer integration on our next-generation ultrasound scanners and further develop our test tools and laboratories.

As our new Senior Test Engineer, your typical tasks will include measurements of sound pressure, acoustic power, thermal characteristics, image performance and other transducer properties.

You will take part in hands-on work while also playing a key role in maintaining and further developing our transducer integration processes and two laboratories.

Technical Drawing Engineer

Would you like to play a critical role in implementing, overseeing and management of key deliverables, and manage the repository of approved technical and regulatory drawing at Bavarian Nordic?

You will establish corporate drawing standards, manage drafting updates carried out by 3rd parties, and oversee the administration of drawing management using multiple software systems.

Customer Service & Logistics Coordinator for medical device company

Contura International A/S is looking for a Customer Service & Logistics Coordinator to join our Facility & Office Management Department.

Your main responsibilities will include but are not limited to:

• Ensuring customer satisfaction through focused communication and support
• Efficiently managing order fulfillment, including the coordination of worldwide shipments in compliance with GDP regulations

As a Customer Service & Logistics Coordinator, you will be joining a company with an ambitious and dedicated team of 100+ employees with direct report to the Facility & Customer Relations Manager.

Senior QA Specialist

The Senior QA Specialist for Radiometer is responsible for ensuring safe, reliable, and compliant products during new product development and maintenance of existing product platforms. This is done by cooperating, supporting, facilitating, training, and communicating towards the best results with partners in R&D.

This position is part of the QA Design Control department, hybrid based and located in Brønshøj. At Radiometer, our vision is to improve global healthcare with reliable, fast, and easy patient diagnoses.

QA Specialist

You will be responsible for ensuring safe, reliable, and compliant products during new product development and maintenance of existing product platforms.

You will have the opportunity to:

• Provide Design Control guidance for QMS and regulatory compliance in an FDA regulated and ISO compliant environment.
• Represent Quality Assurance in design and development projects and in cross-functional teams supporting new product development.

Clinical Evidence Lead

Do you want to:

• Lead the clinical development and clinical data strategy across application areas
• Lead the wording, substantiation, and documentation of clinical claims for regulatory compliance and commercial utilization
• Contribute to the clinical evidence activities in development projects and give input to PMCF

The main responsibilities of your new team are to drive the clinical strategies to ensure timely execution on clinical deliverables to support regulatory submissions and commercial strategies.

Senior Clinical Scientist

Do you want to:

• Execute clinical evaluation and documentation activities, including clinical input to PMCF and PMS.
• Provide clinical support to global registrations.
• Support and drive ad hoc clinical activities and problem solving

The main responsibilities of our Clinical Development team are to drive the clinical strategies to ensure timely execution on clinical deliverables to support regulatory submissions and commercial strategies.