Quality Project Lead

This is a temporary contractor opportunity at Novartis

Novartis touches the lives of a tenth of the world’s population. Every role here, regardless of contract type, makes an impact on human life!

This role is offered through Magnit Global, who, if selected, will be your employer. If your services are retained, you will be assigned to provide services to Novartis as the end client. This is not an offer of employment with Novartis. If you are selected for this Temporary/External opportunity, you will not be an employee of Novartis and will not be eligible for any Novartis employee benefits or incentives.

Ready to work with/through Magnit at Novartis? Please read on…

Lead and support complex projects and quality initiatives. Drive small sub team as part of a matrix organization. Expertise in medical devices. Lead, guide and support global GDPD (Global Device and Packaging Development, Technical Research and Development) project teams in all quality-relevant topics, questions, and issues. Develop project strategies in alignment with GDPD considering all relevant cross-functional aspects to ensure the quality of deliverables within the project.

QA DDS (QA Drug Delivery Systems) representative at expert panel;
Lead and support QA aspects of new technology projects.

• Lead and support global GDPD project teams, and represent QA DDS globally in project sub-teams, as well as at global quality board meetings and project development gate meetings.
• Ensure quality oversight on the assigned development projects with strong quality guidance, scientific and technical expertise.
• Contribute to the strategy of assigned projects incl. contingency planning and risk assessments as appropriate to ensure timely achievement of project quality deliverables. Ensure that the strategy followed within the assigned projects is in line with QA DDS strategies and goals and in compliance to external and internal medical devices requirements and processes.
• Understand and proactively manage the interactions of project related activities between QA DDS and other departments inside or outside of QA DDS.
• Proactively communicate overall project strategy, key issues and any other critical topics in a timely manner to the appropriate management level, to the GDPD project leader and/or to any other relevant project team member(s).
• Provide input to contracts and QA agreements with 3rd parties. Approve project-specific QA agreement amendments for assigned projects.
• Lead or participate in global and/or cross-functional initiatives.

• Bachelor (> 10 years’ pharma quality or operations) or Masters (> 5 years’ pharma quality or operations)
• Fluent English required (oral & written). Good skills in site (local) language desired (oral).
• Fundamental, broad understanding and knowledge of quality standards and policies in Medical Devices manufacturing and control.
• Experience with Notified Body Inspections.
• Broad experience in device development as well as in Quality Assurance and/or Quality Control departments.
• Proven track record in successfully leading interdisciplinary teams, e.g. scientists working on technical or methodological projects, in TRD or equivalent experience from external company or other line function.
• Ability to contribute to matrix teams with the necessary strategic thinking, quality awareness and implementation skills.
• Computer literacy (e.g. MS Office, document management systems) demonstrated along with readiness to learn new systems and associated processes.

Workload
: 40 hours/week

Role type
:
Onsite

Required start date
:
August 2026

Contract
: 11 months

Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.

If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to Magnit at directs