Technical and Manufacturing Manager

2 weeks ago


Stockholm, Stockholm, Sweden Navamedic ASA Full time

If you have expertise in tablet technology and want to join an exciting pharma company in growth and development, keep reading

Navamedic is going through an exciting period of growth, acquiring ownership of products with global market potential. They are now seeking an experienced and highly skilled professional in the manufacturing and quality/technical documentation of medicinal products, combination products, and medical devices. This newly created role is of high strategic importance to Navamedic. The ideal candidate should have experience in galenic pharmacy/tablet technology development, and manufacturing. To thrive in this role, strong business acumen, the ability to find constructive solutions, and the flexibility to handle various tasks are needed.

About the company:

As a Nordic pharma company with a presence in Northern Europe, Navamedic supplies medicinal products, medical devices, medical nutrition, and high-quality consumer health products to hospitals and pharmacies. Navamedic collaborates with distributors and partners to expand into new markets. All the manufacturing is outsourced.

Today, the company has 45 employees has presence in 5 markets.

The position can be placed either in their Stockholm, Gothenburg or Oslo Office.

For more information:

MAIN RESPONSIBILITIES:

Medicinal products:

  • Collaborate with external contractors (CMO) to secure efficient processes and manufacturing of Navamedic owned medicinal products according to GMP.
  • Driving specific technical projects such as tech transfers in compliance with cGMP.
  • Evaluation, selection, and contribute to negotiations with technical/supply CRO/CMOs.
  • Development and maintenance of CMC documentation in collaboration with regulatory department in Navamedic.
  • Collaborate with cross-functional teams ensuring optimizing existing processes and products.

Medical Device/combination products:

  • Coordination and execution of technical activities related to devices and combination products, for externally manufactured products, to support reliable product supply and quality.
  • Development and maintenance of technical files for medical devices, including the device part of combination products.
  • Digital medical devices in development.

KEY REQUIREMENTS:

  • Master of Science in Pharmacy or equivalent degree.
  • Experienced in galenic pharmacy/tablet technology development and manufacturing.
  • Regulatory/GMP of medicinal products.
  • Experience working with Contract Manufacturing Organisations (CMOs), other external vendors, and suppliers, and maintaining successful partnerships.
  • Capability to knowledgably review regulatory technical content in the CMC area.
  • Preferably knowledge of applicable regulatory standards EU Medical Devices and Combination Products.
  • Project management.
  • Strong computer skills, including SharePoint, Word, Excel, and PowerPoint
  • Quality focus.
  • Strong written and verbal communication skills in English, and able to communicate and understand a Scandinavian language (Norwegian, Swedish, or Danish).
  • Critical thinking and analytical skills.
  • Emotional intelligence and decision-making skills.

We invite you to be part of Navamedic's exciting expansion phase. This is a unique opportunity to join the dynamic team at Navamedic, and we look forward to your application.


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