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Biocompatibility Specialist

We are looking for a Biocompatibility Specialist to join the Reprocessing and Biocompatibility team for a 12-month project position.

This is a great opportunity if you would like to gain experience with biocompatibility for advanced reusable medical devices, as you will be part of a cross-functional effort on documenting the safety and performance through the lifetime of our ultrasound scanners, transducers, and accessories.

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.

Procesingeniør til pharmaprojekter

Vil du arbejde med spændende og varierende projekter inden for procesdesign og kunne du tænke dig at blive del af et dygtigt tværfagligt team, hvor humøret og ambitionerne er tårnhøje?

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

• designe, projektere, udføre kvalitetskontrol samt idriftsættelse af produktionssystemer
• bidrage med din procesindsigt og kendskab til anlægsdesign
• indgå som procesingeniør og/eller pakkeejer i projekterne
• indgå i Annex 1 compliance projekter

Projektleder med erfaring indenfor Pharmaindustrien

Vil du arbejde med spændende og varierende projekter inden for Pharma og Biotech og kunne du tænke dig at blive del af et dygtigt tværfagligt team, hvor humøret og ambitionerne er tårnhøje?

Helt konkret vil du arbejde med:

• ledelse af projekter med stor spredning i størrelsesorden fra 1-50 mio. DKK
• ledelse af tværfaglige projekter med leverancer indenfor Process, Mekanik, Automation, El, Instrumentering, Q, HSE samt Byg
• rådgivning- og konsulentopgaver

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.