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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.

Operations Data Coordinator for Drug Substance Production

The primary task within the position is to collaborate with various departments (e.g., automation, tech transfer, and manufacturing departments) to collect and translate information required for building efficient production campaigns and daily task schedules.

You will be part of a team with a great sense of humor and a high willingness to support where needed.

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.

Scientist for Biomarker Assays

Are you eager to use your scientific skills and expertise in preclinical research?

As our new scientist, your tasks will include:

• Coordination and support of biomarker experiments, including supervision of lab technicians.
• Perform data analysis, interpretation, review, and reporting of study results.
• Development of new biochemical- and immunoassays and troubleshooting of existing assays.

Application Technologist

Tetra Pak Filtration Solutions is searching for an Application Technologist in the field of membrane filtration of milk and whey products, with the focus on optimizing the environment footprint and applications.

As an Application Technologist, your responsibilities will be:

• Planning, execution and documentation of technology and application testing at customers site and in our development center.
• Data collection from full scale systems in operation, with focus on optimizing system performance and membrane selection.

We offer you an equal opportunity employment experience that values diversity and inclusion Market competitive compensation and benefits with flexible working arrangements.

Entrepreneurial Immunologist for Applied Research

Would you like to be part of an exciting journey of generating scientific insights on the health effects of human milk oligosaccharides (HMOs), in addition to further improving infant formulas by bringing them closer to breastmilk?

As our senior immunologist, you will be a key member of the Applied HMOs team by leading our immunology platform. Your primary role will be to ensure a strong platform both by running existing in vitro assays and by establishing novel experimental immunological workflows. You will work closely with our commercial team and will also be involved in meetings with customers.

Senior Life Science Business Consultant

Are you an experienced Senior Life Science Business Consultant with a passion for combining life sciences with the business aspects of consulting?

Don't miss this opportunity to advance your career and collaborate with our skilled colleagues to transform the digital landscape for clients all over the world.

You will plan and execute projects for our clients – working collaboratively with others. You will be deeply involved in all project phases from the idea phase, to identifying the value adding areas, analyzing current and future processes and technology needs, vendor selection and implementation.

Clinical Project Manager

Do you want impact, freedom to perform, global perspective and super colleagues?

As experienced Clinical Project Manager, you naturally know that your success is built on your ability to generate high quality data at high pace and within agreed budgets – without jeopardizing the good relationship to the people and partners involved. Another vital part of your road to success is your ability to think outside the box and handle (unforeseen) challenges on the way.

(Senior) Drug Substance Specialist

We are currently seeking a (Senior) Drug Substance Specialist who is energized by collaborative and fun teamwork, excels in handling complex tasks, and enjoys continuous learning.

Your responsibilities will include late-stage drug substance development, up-scaling and process validation as well as support in the commercial phase. Effective coordination with external partners is a significant aspect of this role.

Ambitious Project Manager to lead key strategic projects

Are you an experienced Project Manager motivated by making a difference? Then look no further – Pharmacosmos is looking for a Project Manager who can solve complex problems across our value chain and deliver impact to the organisation.

As Project Manager, you will become a key member of a small project management team in Pharmacosmos. You will be allocated to important strategic projects that you will lead and drive to completion to the satisfaction of all involved stakeholders using your existing toolbox and competencies for managing projects.

Senior Scientist, Infectious Disease Vaccine Discovery and Research

You will conduct various laboratory activities with the primary goal of producing reliable test results and optimizing lab procedures while adhering to correct procedures as well as health and safety guidelines. The role also includes documentation and reporting of results both in writing and in different forums.

You will work with dedicated colleagues in an inspiring and fast-moving environment with a collaborative and innovative spirit.

Senior QA Specialist

You will be part of our QA Business Support Team, consisting of 12 QA Specialists and Senior QA Specialists, allocated to projects including innovation projects, capacity projects and strategic QA/QC projects. We participate in projects both as quality and compliance experts to ensure compliance with the requirements for Class III Medical Devices.

We are driven by improving patient outcomes and we take our values to work every day – we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions.

Senior LIMS Specialist for Global QC Development

In this role you’ll make an impact by working as a Senior LIMS Specialist in our team, where you will take part in management of projects for LIMS changes across QC laboratories and other stakeholders including implementation, documentation and communication.

Future projects could be introducing and validating LIMS solutions on new equipment or technologies, new LIMS functionalities, improving and aligning existing processes.

Regulatory Affairs Clinical Specialist

Due to many activities in our exciting clinical development projects, we are seeking two new colleagues to our Regulatory Affairs function.

Your key responsibilities will be to contribute with regulatory expertise to global strategies and execution within your assigned project(s). You will be the regulatory responsible in the clinical trial teams and provide regulatory guidance and support for the planning, execution, and reporting of clinical trials worldwide.

Business Developer with a background in Science

Do you want to be at the forefront of Targeted Radiopharmaceuticals and Molecular Imaging?

We are looking for a professional Business Developer with a background in life sciences and the ambition to contribute to further strengthening Minerva Imaging as the trusted partner for targeted radiopharmaceuticals and molecular imaging.

What truly matters is your passion for the advancement and know-how of our scientific studies and your ability to foster long-term relationships with our collaborators.

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.

Dyrlæge til moderne og kompetent

Dyrlægehuset Randers søger en dygtig dyrlæge, der brænder for at levere den bedste behandling til klinikkens patienter. Så hvis du har lyst til tage del i en organisation, der vægter et højt fagligt niveau og kollegialt fællesskab, er dette måske jobbet for dig.

Hos Dyrlægehuset Randers behandler de familiedyr i deres fire konsultationsrum samt operationsstue. De er alle udstyret med det moderne teknologisk udstyr, der skal til for at kunne udføre et bredt spekter af operationer, undersøgelser og fysioterapi.

Udover at fungere som dyrehospital, er Dyrelægehuset Randers også en døgnåben skadestue, der tager imod henvisninger fra hele Jylland.

Application Specialist – Beverages

Are you passionate about product development within all types of beverages from premium organic CSD's to flavored spirits?

You will work in a high-paced, collaborative and energetic environment optimizing key elements of beverage applications such as taste, stability, preservation and appearance with the goal to design the perfect balance between these elements.

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.