Senior Quality Academic for R&D Quality

Can you assure quality for clinical trials in order to safeguard subjects safety and well-being?

If you have a thorough experience within GMP, requirements for development of biopharmaceuticals, requirements for Investigational Medicinal Products for use in clinical trials and conducting external audits of CMOs and you are a structured and systematic team player, who dreams of a job with major responsibility and the license to impact decisions, you might be just the person we are looking for.  

Professional about Quality

In this position, you will furthermore play a key role in implementation of quality strategies widely in the organization.

You will also be responsible for:

  • the quality assurance activities in support of the development projects
  • release of Active Pharmaceutical Ingredients, raw materials and excipients for clinical trials
  • release of Investigational Medicinal products for clinical trials
  • establishing and maintaining quality agreements and supplier evaluations

You will collaborate with CMOs as well as colleagues across the organisation. You should be able to deal with complex situations and find compliant solutions together with the stakeholders, even in diverging opinions you should be capable to achieve the right level of compliance.

Experienced GMP specialist with a strong quality mind-set

  • You hold an MSc degree within Pharmacy or equivalent relevant scientific discipline and you have +8 years of experience from the pharmaceutical industry together with a fundamental knowledge within CMC development or production
  • You are a bright communicator and can without difficulty explain complicated matters in an easy understandable way
  • You are curious about understanding people and always respect others and you keep an open mind and see the positive side
  • You are proficient in both written and spoken English

Welcome to R&D Quality in Ballerup

You will be part of R&D Quality a team of 10 enthusiastic, bright and experienced colleagues who all strive to challenge and drive the Quality path forward to ensure the success of LEO Pharma.

 

We look forward to receiving your application.

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About LEO Pharma
LEO Pharma helps people achieve healthy skin. By offering care solutions to patients in more than 100 countries globally, LEO Pharma supports people in managing their skin conditions.
Founded in 1908 and owned by the LEO Foundation, the healthcare company has devoted decades of research and development to delivering products and solutions to people with skin conditions.
LEO Pharma is headquartered in Denmark and employs around 4,800 people worldwide.
For more information, visit www.leo-pharma.com.
Application deadline: 04/03/2018

Location: Ballerup, Greater Copenhagen, DK

Job type: Permanent

Working hours: Full-time

Contacts: Marianne Bergholt Schmidt
Mobile: +45 3116 4633