Expert Engineering (m/f/d)

Salary Range:

Job Description Summary

Role Purpose:

Are you looking for a challenging and rewarding career in Combination Product Development with a brand new device? Do you want to be part of a team of talented and passionate engineers and scientists who are responsible for the development of parenteral combination products to ensure that our delivery systems fulfil the highest customer expectations? If yes, then this is the opportunity for you! The Device Technology Solution Center is seeking an Expert Engineering within the Global Device and Packaging Development (GDPD) department in Schaftenau, Austria.

Job Description

Key Responsibilities:

• Deliver technical development and life-cycle management in cross-functional teams for easy-to-use, safe and robust products.

• Responsible for device constituent parts of an autoinjector, the system integration of prefilled syringes together with the autoinjector into a combination product and timely delivery of technical aspects of one or more projects as well as LCM of commercial products.

• Support device design development following the design control process and applicable regulatory framework

• Ensure components are delivered and controlled to the required quality for clinical trials and commercial production.

• Support internal & external audits on medical devices related matters and provide input to health authority questions.

Essential Requirements:

• Bachelor, Master or PhD degree in engineering or equivalent

• Preferably 2+ years of experience working in development of medical device and/or combination products; preferred in pharmaceutical area or similar. Less Experienced applicants could be considered under certain circumstances within another lower job band as Expert Engineering.

• Experience in developing plastic and metal components; tolerance analysis, modelling and testing

• Excellent skills in English, verbal and written. German language skills are of advantage

• Autonomous and independent working style with interest to work in medical device development and life cycle management projects.

• Ability to interact with cross functional team in matrix organization.

Adjustments for Applicants with Disabilities:

If because of a medical condition, physical disability or a neurodiverse condition you require an adjustment during the recruitment process, please reach out to [email protected] and let us know the nature of your request as well as your contact information. The support which we can provide will include advice on suitable positions as well as guidance at all stages of the application process. Austrian law provides candidates the opportunity to involve the local disability representative, Behindertenvertrauensperson (BVP), in the application process. If you would like to request this, please let us know in advance as a note on your CV.

Benefits & Rewards

At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen.

Expected Annual Base Salary Range for role: € 60,978 to € 96,200

The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically.

In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters.

The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave.

Skills Desired