Program Manager – Tech transfer/process development
- Denmark
- Contract
- Life Sciences
This vacancy has now expired
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.
- 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)
The candidate must have the rights to work in the location stated in the job advert.
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I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
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