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Device Industrialisation Engineer (Hybrid)
TN United Kingdom
Cambridge
On-site
GBP 80,000 - 100,000
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Job summary
An established industry player in the pharmaceutical sector is seeking passionate individuals to join their innovative team. This role offers a unique opportunity to contribute to the development and scale-up of sustainable generic and biosimilar medicines. As a key member of the team, you will leverage your expertise in tech transfer, supplier management, and process development to ensure the successful transition of products from R&D to production. This is an exciting time for the organization as it embarks on a transformative journey, and your contributions will play a vital role in shaping the future of healthcare. If you are ready to make a significant impact, this opportunity is perfect for you.
Qualifications
- Experience in tech transfer for medical/pharma products.
- Expertise in process development and scale-up activities.
Responsibilities
- Work within a matrix management structure in a larger organization.
- Provide expertise in device scale-up and validation methods.
Skills
Teamwork in matrix management
Tech transfer activities
Supplier management
Process development tools
Device scale-up activities
Tools
Validation methods
Medical device assembly tools
Packaging equipment
Job description
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Novartis
Cambridge, United Kingdom
-
Yes
ca26da8c762d
41
30.03.2025
14.05.2025
Sandoz is going through an exciting and transformative period as a global leader and pioneering provider of sustainable Generic and Biosimilar medicines.
Now as an independently listed company, Sandoz aims to increase its strategic focus, operate with greater agility, set clearer business objectives, enhance shareholder returns, and strengthen its culture for us, the Sandoz associates. This is an exciting time in our history, and by creating a new and ambitious path, it will provide a unique opportunity for us all, both professionally and personally.
Join us as a Founder of our ‘new’ Sandoz!
Your Key Responsibilities:
- Experience of working in a team within a matrix management structure within a larger organization
- Knowledge and experience of tech transfer activities for medical/pharma products moving from R&D into production
- Knowledge and experience in supplier management and capital equipment acquisition
- Knowledge and experience of process development tools and industry-accepted validation methods
- Provide expertise and input into device scale-up activities including DFM; DFA, precision component moulding and assembly.
- Specialist expertise knowledge area in one or more of the following:
- Process development & scale-up
- DFM/precision medical component moulding
- DFA/ precision medical device assembly
- Primary packaging including sterile injectables, selection, fill-finish and assembly
- Secondary & Tertiary packaging for medical/pharma products, development and manufacturing
- Shipping & transport development & testing for medical/pharma products
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