Skip to main content

Program Manager – Tech transfer/process development

  1. Denmark
  1. Contract
Competitive
25564/ZM
  1. Life Sciences
Date Posted07 Oct 2020
 Program Manager – Tech transfer/process development

Denmark is a hive of activity for the Life Sciences Industry at present with no shortage of major expansion/ new build facilities. We have an exciting opportunity for a Program Manager within Technology Transfer/Process Development to join a major project for a global biotech organisation, located in Denmark, with great longevity of employment possibility.

Key Responsibilities:
  • Responsible for program management within Technology Transfer related to Large Scale Drug substance manufacture at the Hilleroed site.
  • Bringing DS internal and partnered programs from development through PPQ to commercial manufacture.
  • Responsible for the technical transfer and scale–up of new processes within a dynamic CDMO DS environment.
  • Ensure the highest Quality, Compliance and Safety standards primarily with Technology Transfer but relating to all activities.
  • Work within a team to enable the team’s performance within the Manufacturing Science and technology group.
  • Technical Review and ownership of Global Change management records as required.
  • Recommend technical approaches in line with global and local standards.
  • Benchmark and remain current with development of new technologies in the biopharmaceutical processing field of expertise and seek to deploy process improvements through innovation and utilization of these technological advances.
  • Contribute for driving a culture of Continuous Improvement by deploying Merck Six Sigma tools and MPS within the site on projects such as:  problem solving, reducing cycle time, Lean principles within the new processes.
  • Stakeholder management of multiple decision makers, corporate colleagues, cross-functional team by demonstrating the ability to maintain and strengthen trust relationships with people on all levels.
This job might be for you if you have:
  • Experience in biopharmaceutical drug substance environment and a background of working within a CDMO.
  • Hon. Degree or Masters in a Science or Engineering discipline (preferably Biotechnology).  
  • Project management qualification such as, Project Management Professional is desirable
  • Evidence of Continuous Professional Development
  • Demonstrated knowledge in Biopharmaceutical operation (e.g. manufacturing, technology, validation, engineering, quality or analytical.).
  • Demonstrated knowledge of managing a Technology Transfer within Biopharmaceutical industry (process or analytical)
For more information on this project / position, please apply with a copy of your up to date CV today! 




The candidate must have the rights to work in the location stated in the job advert.

Please note, Quanta Consultancy Services does not sponsor Visa applications.

To view Quanta's privacy policy, please visit our website

Similar Jobs

Options: Contract
Location

Denmark

Description

Drug Product MSAT Scientist Denmark is a hive of activity for the Life Sciences Industry at present with no shortage of major expansion/ new build facilities. We have an exciting opportunity for

Options: Contract
Location

Denmark

Description

Upstream Manufacturing Technology (MT) Scientist Denmark is a hive of activity for the Life Sciences Industry at present with no shortage of major expansion/ new build facilities. We have an

Options: Contract
Location

Denmark

Description

Downstream Manufacturing Technology (MT) Scientist Denmark is a hive of activity for the Life Sciences Industry at present with no shortage of major expansion/ new build facilities. We have an

Send us your CV

Our candidates are the cornerstone of our organisation and we are always looking to connect with new professionals who are seeking their next contract assignment or career opportunity.