Job opportunities

Pharmaceutical Specialist

Location

Region Hovedstaden

City

Copenhagen

Department

Research and Development

Application deadline

27 September 2017

Description

Pharmaceutical Specialist, Biologics – Pharmaceutical Development & Manufacturing

Would you like to be a part of setting the strategic direction within formulation development on key biologics projects? Do you possess a creative mind-set and strategic skills? Do you enjoy solving complex scientific challenges in an environment where prerequisites and timelines may change overnight? Then you may be our new Pharmaceutical Specialist within Biologics.
In Pharmaceutical Development & Manufacturing we are 17 highly skilled and passionate colleagues who are focused on pharmaceutical development of all clinical and commercial formulations from early phase development to commercial implementation and life cycle management. The department works with both small molecules and biologics. As a part of our new strategy we have an increased focus on biologics in the CMC area and an important part of this new position is to provide scientific and strategic leadership for pharmaceutical development activities in support of our biologics pipeline (mAbs), spanning pre-IND stage through validation and launch.
The department is part of Chemical and Pharmaceutical Research (CMC development) located in Valby. Our focus in CPR is to support the development of new drug candidates within depression, schizophrenia, Parkinson’s disease and Alzheimer’s disease. We strive to develop new innovating treatments to help improve the lives of the patients suffering from these diseases.
The ideal candidate is an experienced Pharmaceutical Specialist with experience with biologics. You will enjoy playing a key role in applying scientific knowledge and expertise to propose new areas to explore and expand our scientific know-how. You will work with a wide variety of exciting activities in close collaboration with colleagues in your team and across the organization from Research to production. You will also play an important role in the collaboration and expectation management with our CRO’s and CMO’s as most activities for biologics are currently outsourced.

Your job and key responsibilities
You will be responsible for development of pharmaceutical formulations and processes to support our global development projects, with primary focus on the biologics projects.

You will be an active part of the CMC project team, where your main tasks will include:

  • Strategic leadership for formulation development on key projects and assist in setting the strategic direction for general work with biologics project in the area.
  • Defining the right formulation strategy and design and lead formulation development activities
  • Close collaboration and coordination of work carried out in collaboration with CRO/CMO’s.
  • Responsible for setting up and reporting formulation and process development work at CRO’s and ensure proper documentation both for internal and regulatory purposes.
  • Scientific responsibility for IMP productions at CMO’s in various scales in close collaboration with GMP personnel will also be part of your tasks.
  • Share scientific knowledge and technological understanding with dedicated colleagues across the organization to support our projects.

Qualifications
Our preferred candidate has the following personal and professional qualifications:

  • You hold a PhD or a MSc within pharmaceutical science, engineering or another relevant scientific discipline
  • You must have a minimum of 7 years of relevant experience and proven scientific skills within drug product development for biologics products
  • Possess a deep understanding of the different formulation development phases including knowledge about regulatory and quality aspects of drug development projects.  
  • You are experienced in leading development activities, result-oriented and able to manage problem solving in a structured manner and find innovative solutions if needed.
  • As a person you possess a personal drive, a positive mind-set and enjoy working in a busy and team based environment.
  • You strive to set high scientific standards and are attentive to details and good documentation standards.
  • You work well in teams and interact easily with people on all levels. You thrive equally well in situations where you provide scientific sparring for colleagues or as leader of development activities.
  • You have excellent communication skills both verbally and written (English).

Further information

For further information, please contact Senior Director of Pharmaceutical R&D Frank Høien Lendal on FHK@lundbeck.com or + 45 30 83 23 99 or Director of Pharmaceutical Development & Manufacturing Kirstine Høeg-Møller on KIRB@lundbeck.com or +45 30 83 35 98.

Your application and CV should not be sent via email.

We also recommend that you have a look at our website.

Your application

Please click on the link below to apply for the job. Applications must be received no later than 27 09 2017.

 

 

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Lundbeck is a global pharmaceutical company specialized in psychiatric and neurological disorders. For more than 70 years, we have been at the forefront of research within neuroscience. Our key areas of focus are depression, schizophrenia, Parkinson's disease and Alzheimer's disease.

An estimated 700 million people worldwide are living with psychiatric and neurological disorders and far too many suffer due to inadequate treatment, discrimination, a reduced number of working days, early retirement and other unnecessary consequences. Every day, we strive for improved treatment and a better life for people living with psychiatric and neurological disorders – we call this Progress in Mind.

Read more at http://www.lundbeck.com/global/about-us/progress-in-mind.

Our approximately 5,300 employees in 55 countries are engaged in the entire value chain throughout research, development, production, marketing and sales. Our pipeline consists of several late-stage development programmes and our products are available in more than 100 countries. We have research centres in China and Denmark and production facilities in China, Denmark, France and Italy. Lundbeck generated revenue of DKK 14.6 billion in 2015 (EUR 2 billion; USD 2.2 billion).

For additional information, we encourage you to visit our corporate site www.lundbeck.com and connect with us on Twitter at @Lundbeck .

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