Principal Analytical Scientist – Biopharmaceutical Products

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Are you a biopharmaceutical scientist with experiences in characterization and analytical development of proteins in late stage clinical development, and are you looking for a job with exciting scientific challenges and the opportunity to use and develop your strategic mindset? Do you have experience from working with external partners and CRO/CMO´s, and is this something that gives you energy? Then this may just be the job for you.

LEO Pharma has embarked on a growth journey to become the preferred dermatology care partner in the world, dedicated to help people achieve healthy skin. We have an ambitious 2030 strategy, which aims to accelerate our impact in innovative therapeutics while strengthening our established portfolio and our global footprint in medical dermatology. Dermatology is an area of rapid growth and LEO Pharma´s vision is to reach 125 mill. patients worldwide by 2025. Biopharmaceutical Products is one of two departments (the other being Biopharmaceutical Processes) within CMC Design and Development within LEO Pharma focusing on the CMC development of biologics. The departments were started in 2017 with a strong focus on building biologics CMC capabilities within LEO to support a growing pipeline on monoclonal antibodies (mAbs). This is why we need you!

The role

In Biopharmaceutical Products, you will join 17 highly skilled and experienced persons constituted by Formulation and Analytical Scientists and Technicians, all with the focus on developing biologics products from discovery to market. All projects are run as external partnerships with extensive CDMO/CRO collaborations. The department is responsible for all CMC product activities throughout the full value chain for monoclonal antibodies including; developability studies, development of formulations and analytical methods, preparation of module 3 documentation, feasibility studies and IMP productions.

As a principal analytical scientist your essential tasks will be

  • Setting development strategies for activities associated with our mAb products
  • Participate in CMC teams and project work. Collaborate with team members from different departments within development
  • Lead, plan and document development work related to characterization, release testing, stability studies, specifications and reference standards, as well as analytical method development, validation and transfer
  • Manage selection and oversight of contract laboratories and contract manufacturers for analytical workpackages
  • Coordinate activities at CRO/CDMO assuring adherence to agreed timelines and quality standards
  • Write, elaborate and contribute to relevant regulatory documents
  • Initiate/introduce new scientific know-how and keep an updated scientific and regulatory knowledge in the areas of analytical development and characterisation of proteins

Qualifications

We expect the ideal candidate to:

  • Have minimum a M.Sc., but preferable a Ph.D. in pharmaceutical sciences, chemical engineering or equivalent education
  • Have solid and relevant experience from biopharmaceutical industry
  • Have proven scientific skills in analytical development for protein in late phase development (Phase 3), experience with potency assay is a plus
  • Have experience in outsourcing and coordinating activities with CMO/CROs
  • Be familiar with GMP and regulatory guidelines
  • Be able to obtain a good overview, prioritize and take full responsibility of an assignment
  • Be innovative, flexible and quality minded
  • Have excellent communication skills and be fluent in English, both spoken and written

Additional information

For additional information, please contact Senior Manager Christer Andersson +45 31385986 , [email protected] or Senior Manager Kristoffer Toemmeraas, [email protected]. Send your application and CV in English as soon as possible and no later than 17 November 2020 as we will review incoming applications on an on-going basis.

About LEO Pharma

LEO Pharma LEO Pharma is on an exciting journey of transformation to become the world leader in dermatology. We keep the patients at the heart of everything we do, and we drive dermatology with our knowledge, collaboration and curiosity. We are at the forefront of science in developing new medicines for dermatology, and we are committed to helping people with skin diseases live more fulfilling lives.

Our people are united worldwide with strong core values and a common vision. Our shared vision and mission adapt to an ever-changing environment, while remaining true to our business strategy. Our values reflect the way we strive to increase the quality of life for patients.

Founded in 1908 and owned by the LEO Foundation, LEO Pharma has devoted decades of research and development to advance the science of dermatology, setting new standards of care for people with skin conditions. LEO Pharma is headquartered in Denmark with a global team of 6,000 people, serving 92 million patients in 130 countries.


Information og data

Denne ledige stilling har jobtypen "Forsker", og befinder sig i kategorien "Sundhed og forskning".

Arbejdsstedet er beliggende i Ballerup.

Jobbet er oprettet på vores service den 30.10.2020, men kan have været deaktiveret og genaktiveret igen.

Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
  • Forsker
  • Ballerup
  • Tirsdag den 17. november 2020

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