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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.

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.

Sales Trader

We are looking for a Sales Trader who will play a vital role in ensuring BioCirc’s ambitious growth plans.

The successful candidate will together with the Portfolio Manager be responsible for the short-term sale of Certificates, optimizing the portfolio, gather market intelligence, and ensuring value added through the whole supply chain of biomethane production, but also new renewable products stemming from our energy clusters.

HSE Specialist

As an HSE Specialist, you will have the opportunity to develop and implement safety policies and procedures, conduct training sessions, and ensure compliance with local, state, and federal regulations.

In joining our team, you'll have the opportunity to make a significant impact, ensuring the safety and well-being of our workforce while contributing to our continued success at Duferco Danish Steel.

Senior Specialist Clinical Safety and Pharmacovigilance (CSPV)

At Bavarian Nordic, we aspire to save and improve lives by developing innovative vaccines that are designed to unlock the power of the immune system.

The global team consists of subject matter experts for vaccine safety who work either from our site or remotely in Denmark and globally. Together they constantly collect and assess data for the life cycle benefit risk management across our vaccines whether authorized or still in clinical development.

You would add your clinical safety and pharmacovigilance expertise as your depth knowledge of the PV legislation to the team.

Senior Process Specialist

Do you want to be part of Process Support in a company with a unique impact on global healthcare? Grab this opportunity to be part of a fast-growing company ready to invest in you.

You will become a process owner of one or more of our production processes in SFI. This means that you will be responsible for, among other things, validation documentation, revalidations, and risk assessments for the specific process.

Project Coordinator

Do you have experience managing projects anchored to a GMP facility? Are you eager to contribute to the development of a newly established project team in a production environment?

As a Project Coordinator, you will participate in the successful planning and completion of projects related to the Drug Substance Manufacturing Processes. You will coordinate and follow up on a number of tracks that links to various projects.

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.

Project Leader – process/hydrogen safety

Do you want to apply your skills to promote a fast and safe transition of the energy and transportation sectors away from carbon-based fuels?

You will be leading diverse teams of experts to deliver state-of-the-art results to our partners in the hydrogen sector, working on some of our largest fire safety projects.

We have great offices and facilities, and you get good staffing conditions, such as pension scheme, dental insurance, and health insurance. We have an active staff and art association, and our chefs cook delicious food for us daily.

Battery specialist

Do you want to apply your skills to promote a fast and safe transition of the energy and transportation sectors away from carbon-based fuels? Do you have experience working with or developing battery technologies?

As our new Battery Fire Specialist, you will provide expertise on Li-ion batteries and other upcoming technologies to the team. You will be part of projects performing risk analyses, battery fire tests, and fire safety design for clients and in R&D contexts.

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.

MS&T Program Manager

We are looking for an experienced professional from the pharmaceutical industry, who can effectively manage project plans across multiple entities and lead cross-functional processes within our own sites and supply chain.

As a MS&T Program Manager, you will be responsible for managing the projects, maintaining project databases, as well as ensuring effective communication and timely achievement of milestones.

Manufacturing Science & Technology (MS&T) Technical Transfer Project Manager (Sr Specialist)

Join Orifarm and take charge of building strong business relationships with a key portfolio of our suppliers!

As a MS&T Technical Transfer Project Manager, you will be responsible for securing technical support to Supplier Relationship Management functions, and manufacturing sites comprising support, technological transfers between CMOs and own manufacturing sites, analytical method development and validation, external product development at CDMOs and driving continuous technological improvement and innovation.

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.

Risk Management Specialist

Are you ready to make a significant impact on industrial safety?

As Risk Management Specialist you will be responsible for conducting HAZID, HAZOP and LOPA studies to identify hazards, deviations, and operability issues.

You will play a key role in risk assessment, analysis, handlings, and mitigation, whilst ensuring compliant documentation and reporting.