Device Engineer (Technical Documentation)
Device Engineer (Technical Documentation)
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Job Description
Job Description Summary
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.
Join us as a Founder of our new Sandoz!
Job Description
Your Key Responsibilities:
Your responsibilities include but not limited to:
Champion Device Engineering activities on projects managing the deliverables and timelines and liaise with the Project Managers / Device Project Leads to ensure successful project outcomes
Drive the creation of quality documentation with a strong focus on Design Input and Design Output stages of the product development lifecycle
Support the creation of quality documentation from other departments including Device Verification User Interface and Industrialisation
Participation and input into Design Reviews
Participation and input into risk assessments such as FEMAs
Liaise with suppliers / partners to assess their offerings and monitor suitability for use in Sandoz products during the product development / procurement process
What youll bring to the role:
Essential Requirements:
Masters PhD or university degree in the field of Mechanical Engineering or other relevant subject
Proficiency in engineering areas such as: tolerance analysis; mechanism design; 3D CAD; component drawings etc.
Some experience in the development of medical devices and/or combination products within a pharmaceutical medical devices and/or combination products setting
Technical knowledge of medical device technology and drug-device combination products
Experience of working within the ISO13485 medical devices quality framework.
Results orientated enthusiastic and driven by excellence
Excellent command of English (verbal and written)
Youll 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 ()
#Sandoz
Skills Desired
Cad Software Creo Elements/Pro Electrical Design Geometric Dimensioning And Tolerancing (GD&T) Mechanical Design Product Design PTC CreoEmployment Type
Full-Time
