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Senior Vice President, Global Chief Medical Office

We are seeking a highly experienced and dynamic medical executive to join our Global Research & Development organisation in a newly established senior leadership role as SVP, Global Chief Medical Office (GCMO).

In this role, you will act as scientific advisor to the EVP of R&D and the Global R&D leadership team, and your primary objective will be to ensure “one global medical voice” for ALK internally and represent the medical voice of ALK externally.

Teamleder søges til moderne system og automationshus

Hos Lund & Sørensen A/S oplever vi en betydelig vækst i efterspørgslen på vores automationsløsninger. For at understøtte denne udvikling søger vi en dygtig teamleder til vores hardwareafdeling.

I denne stilling vil du spille en nøglerolle i en dynamisk og udviklingsorienteret virksomhed, hvor kundens behov og den bedste automationsløsning altid er i fokus.

Nøgleopgaver bliver bl.a.:

• Design og udvikling af el-konstruktioner efter kundernes ønske.
• Være det primære kontaktpunkt for kunder og sikre kundetilfredshed.
• Daglig ledelse og udvikling af medarbejderne i konstruktionsafdelingen.

QEHS Manager

Unique opportunity to join an innovative biotech company with a proven and sustainable technology on the edge of global expansion.

Do you want to help develop the protein of the future, which will make it possible to feed the world's growing population without damaging our ecosystems?

You will be leading a small team responsible for managing and coordinating all QEHS activities, including certifications, audits, and training. You will ensure that operations are conducted in a safe and efficient manner and in conformance with safety regulations.

Regulatory Affairs Manager

The Regulatory Affairs Manager at Radiometer is responsible for managing the preparation and submission of the required documentation for product registration, approval, and compliance with international regulations.

This role is critical for ensuring that Radiometer's products can be sold in markets around the world. You will have the opportunity to:

• Ensure regulatory compliance to maintain market approvals
• Lead a team of skilled RA associates
• Ensure alignment with relevant stakeholders

Site Supervisor

Would you like to be part of an international organization and contribute to an exciting project?

We are looking for a well-organized Site Supervisor with strong leadership skills to join our team at Køge Hospital Project Team I/S.

The Site Supervisor responsibilities include managing different parts of construction projects, supervising crew members, completing quality, requirements, prepare daily reports, observing health and safety standards, and compiling reports for different stakeholders.

Manager, Chemical Substance Registration

The Manager, Chemical Substance Registration is accountable for implementing and executing the chemical control compliance programs of IFF in the EAME region (UK, EU REACH, Turkey REACH, EAEU etc.) for the technical enzymes’ portfolio of products (Biofuels, Fabric & Household Care, Textile Processing and Designed Enzymatic Polysaccharides).

The Manager, Chemical Substance Registration is furthermore a key contact for the Enzyme Business in determining strategic business decisions and should be representing IFF in industry work groups to assure IFF’s regulatory interests.