Device Industrialisation Engineer

Sandoz is going through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic 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.

Your Key Responsibilities:

• Experience of working in a team within a matrix management structure within a larger organisation.
• Provide expertise and input into device scale-up activities including DFM; DFA, precision component moulding and assembly.
• Knowledge and experience in supplier management and capital equipment acquisition.
• Knowledge and experience of process development tools and industry accepted validation methods.
• Knowledge and experience of tech transfer activities for medical/pharma products moving from R&D into production.
• 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

What you’ll bring to the role:

Essential Requirements:

• Experience working in strong matrix teams.
• Experience involving scale-up of complex precision MedTech products and has played a significant role.
• Experience interfacing with leading MedTech CMO's and capital equipment suppliers whilst representing a professional organisation.
• Ability to lead and control interactions to achieve desired outcomes.
• Demonstrable experience of implementing industry standard guidance's and tools (ICH Q8,Q9,Q10 ISO13485, ISO14971, cGMP, CFR210/211).
• Given examples of projects involving tech transfer of MedTech products where candidate played a significant role.
• Specific qualifications, training and/or experience in the listed areas, backed up by demonstrable experience.

You’ll receive:

• Competitive salary
• Annual bonus
• Pension scheme
• Share scheme
• Health insurance
• 24 days annual leave
• Flexible working arrangements
• Employee recognition scheme
• Learning and development opportunities.

Why Sandoz?

Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, touched the lives of almost 500 million patients last year and while we are proud of this achievement, we have an ambition to do more! With investments in new development capabilities, state-of-the-art production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.

Our momentum and entrepreneurial spirit is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is encouraged! The future is ours to shape!

Commitment to Diversity & Inclusion:

We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Join our Sandoz Network:

If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Sandoz and our career opportunities, join the Network here: Sandoz Talentpool (novartis.com)