Quality Specialist to External Manufacturing

A key operational challenge for LEO Pharma will be to ensure GXP and Regulatory compliance in an expanding and increasingly complex network of external manufacturing partners

We need you to join our External Manufacturing Quality team in a newly established position.

Beyond QA responsibilities in relation specific Contract Manufacturer Organizations (CMOs) you will get opportunities to influence the development of a world class Quality Management System for LEO External Manufacturing and to utilize your professional competences in a small dedicated team of Quality specialists .

QA approach based on Quality Oversight and Quality Risk Management

It is our defined goal to succeed in providing continuous quality oversight of LEOs CMOs. In this connection you will have responsibilities within (but not limited to):

  • Establishment of solid, robust and transparent Quality Agreements as framework for the quality related partnership with the CMOs
  • Close Quality relations with CMOs including regularly meetings
  • Periodic quality reviews such as audits and PQR’s

By joining the team you will have an outstanding opportunity to use and develop your professional and personal competences and to contribute to business critical partnerships. Our functional area are developing fast and you must be ready to tackle new challenges in a fast changing professional working environment. You must do this across professional and cultural borders while involving multiple stakeholders internally and externally. Related to this, you can look forward to travel approx. 10-20 days per year to meet partners and colleagues.

Master of Science with excellent QA skills

You hold a University degree within Pharmacy, Engineering or a similar discipline and you have at least 5 years’ relevant experience from the pharmaceutical industry. If you have been working in a similar position, as a QP and/or as an auditor it will be considered an advantage.

You are recognised for your ability to deliver excellent QA results without compromising your personal integrity and long term perspective. You tackle high tasks with high complexity and make fast decisions often by involvement of your colleagues.  

External Manufacturing QA – your new work place

Within the QA for Finished Goods Manufacturing you will join a smaller, international group of skilled and dedicated QA specialist. Your colleagues are having the same role as you meaning you will have great opportunities to share knowledge and contribute to creating best-in-class processes and tools.

We share office with our colleagues in External Manufacturing. We also share aspirations towards being known to be open-minded and ambitious while never forgetting that people who have fun create the best results.

We look forward to receiving your application. Please note that we review applications on an on-going basis.

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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: 27/02/2018

Location: Ballerup, Greater Copenhagen

Job type: Permanent

Working hours: Full-time

Working days: Day

Contacts: Lene Due Svensson
Mobile: +45 9393 2710