Technical Transfer Project Manager, Manufacturing Science

1 week ago

Odense, Denmark Best Talent Full time
Technical Transfer Project Manager, Manufacturing Science & Technology (MS&T), Orifarm / 1877 Best Talent

The Company
In Orifarm, they aim to bring healthy days by making modern healthcare a better deal for the people and the societies they serve. Everyone should have access to modern medicine. High costs or lack of access to pharmaceuticals should never impact possibility to receive treatment or relief and live a healthy life. Working towards that vision, Orifarm creates access to affordable high-quality pharmaceuticals and healthcare products by challenging markets and always seeking new opportunities.

Orifarm was founded in Denmark in 1994. Since then, Orifarm has grown into an international company operating globally in 13 countries. Today, Orifarm is Europe's largest parallel importer of pharmaceuticals and Denmark's largest supplier of pharmaceuticals with more than 2,200 employees.

The Team
You will be part of the Product Supply organization, where Orifarm fosters an ambitious and open atmosphere. You will be closely involved with functional and cross-functional teams:

Working in cross-functional teams with Supplier Relationship Management (SRM), Strategic Procurement, Supply Chain, Quality Assurance (QA) and Orifarm manufacturing sites to effectively transfer and maintain processes and products from a technological point of view.

Technical Transfer Project Manager
Manufacturing Science & Technology (MS&T)
Join Orifarm and take charge of building strong business relationships with a key portfolio of suppliers

  • You lead & support technological projects, transfers, and changes
  • Experience with CMOs & CDMOs, process scaling, manufacturing support and troubleshooting
  • You thrive working in an environment of entrepreneurial spirit

The Challenge
The position will be a part of newly created function, The SRM – Supplier Relationship Management. As MS&T Technical Transfer Project Manager, you will be responsible for securing technical support to the functions and driving continuous technological improvement and innovation. You will drive these process and productivity improvements in manufacturing processes in line with regulatory requirements and business objectives.

Among your key responsibilities in the role, you will be:

  • Leading and supporting technological projects, transfers, and changes (e.g. concerns raw materials, manufacturing process, packaging process, CMC, analytical methodology, specifications) for Contract Manufacturing Organizations (CMOs) or own sites
  • Supporting CMOs in external development of a product, changes, improvement of a manufacturing process, development or improvement of an analytical method, or support during process validation
  • Ensuring that changes to existing processes or the introduction of new processes are carried out according to approved change control procedures and in compliance with cGMP requirements
  • Evaluating existing processes to identify/implement strategic initiatives, and new technologies that improve productivity and quality
  • Communicating on project or transfer status, decisions, prioritizations, and delivering presentations to internal stakeholders and external partners

Your Talent
You have a degree in Pharmacy, Pharmaceutical Engineering, Biotechnology, Chemical Engineering or related fields combined with at least 6 years of relevant experience in the pharmaceutical industry, especially in generics and OTC, preferably also in CHC.

You have demonstrated results and are used to interact with all kinds of various internal stakeholders and external service providers or product suppliers. Therefore, you have a high level of proficiency in influencing across various functions and fostering collaboration across different cultures.

Among the key characteristics of a successful candidate, we expect:

  • Experience with both Pharmaceutical Development and Pharmaceutical Manufacturing as well as experience with both solid and liquid dosage forms, semi-solid dosage forms and sterile liquids processes at small, intermediate, and full scale of cGMP production
  • Technology Transfer experience within and between organizations
  • Experience with CMOs and CDMOs, process scaling, manufacturing support and troubleshooting
  • Advanced Program management and Project management skills including method transfers, and risk assessment

As a person you are result oriented and visionary. You are good at solving complex technical matters and find new solutions. You thrive working in an environment of entrepreneurial spirit surrounded by experienced leaders and colleagues. You have a can-do-attitude and see possibilities instead of problems. You are good at communicating on all levels, like having influence and be involved in decision making.

Application
Best Talent is responsible for the recruitment process at Orifarm and reviews your application on a confidential basis. Forward your application including your CV in English marked ”1877/Tech Transfer” by e-mail to You can read more about Best Talent on

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