Technical Specialist

2 weeks ago


Wrexham, Wrexham, United Kingdom IPSEN Full time

Title:

Technical Specialist

Company:

Ipsen Biopharm Ltd

Do you have hands on experience with Oral Solid Dose (OSD) formulation and manufacturing processes ?

Are you looking for a role without typical organisation borders where you could learn something new every day, broaden your skills whilst using your expertise to deliver products to patients?

Ipsen's External Manufacturing Organisation (EMO) are now recruiting for a Technical Specialist. This is a new position that has been created due to continued business demands.

The role is permanent and can be based at any of the following Ipsen locations:

Slough UK, Wrexham UK, Boulogne France, Signes France or Dublin Ireland This role has a broad remit, offering the opportunity to oversee activities to support an end to end manufacture and analysis of pharmaceutical active substance and drug products.

The day to day activities involves virtual interactions with external manufacturing and testing sites as well as Ipsen wide cross functional internal teams.

Occasional travel to facilitate Face to Face meetings with external partners may be required periodically.


Ipsen is a rapidly growing global biopharmaceutical company focused on innovation and specialty care with sales growth of 21.1% in 2021.

Ipsen aim to make a sustainable difference by significantly improving patients' health and quality of life through differentiated and innovative medicines in oncology, neurosciences, and rare diseases.

We offer employees a wealth of fulfilling challenges and growth opportunities, and the chance to contribute within an agile fast-moving organisation, an organisation that is genuinely game-changing.


  • Hands on experience of solid dose development/ manufacture i.e. Granulation, Milling, Extrusion, Tableting, Encapsulation
  • Knowledge of process validation
  • Ability to Establish technical relationship/s with CMO's & Contract Laboratories to facilitate day to day activities
  • Project management and organization skills to tackle conflicting priorities and deliver against the team's objectives
  • Problem solving, trouble shooting abilities to lead/support investigations into technical issues

Desirables:

  • Experience with new product introduction and Technology Transfer of OSD products
  • Experience with working with/or at an OSD CMO/CDMO
- knowledge of regulatory expectations and responding to regulatory questions (EMA/FDA)

  • Data visualization and trending using statistical tools


To be considered for this role, you will be educated to degree level in scientific discipline preferably chemistry, pharmaceutical science and engineering or equivalent industry experience.

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