TRD Quality Project Lead

WillHire; Basel; Vor Ort; CHF 120.000 - 180.000; Vollzeit

Zusammenfassung

Magnit Global is seeking a QA leader to support global TRD projects for Novartis on a 12-month contract, onsite. You will lead complex quality initiatives, coordinate with cross-functional teams, and ensure compliance with cGMP alongside external partners.

The role requires deep QA expertise in Drug Product/Medical Devices, experience with health authority inspections, and strong communication in English. Start date is 1 January 2027; accommodation through Magnit may apply.

Qualifikationen

• Bachelor >10 years pharma quality or operations
• Fluent English required (oral & written)
• Broad understanding of quality standards and policies in Drug Product/Medical Devices manufacturing and control
• Experience with Health Authority Inspections (FDA/EMA) and RegCMC NB inspections

Aufgaben

• Lead global TRD project teams and QA topics
• Provide quality oversight on development projects
• Guide TRD project teams for Mock-PAI and PAI preparations

Kenntnisse

Quality Assurance

Regulatory compliance

Project management

English fluency

Ausbildung

Bachelor’s degree in Pharma/related field

Tools

MS Office

Jobbeschreibung

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…

Job Purpose:

Lead complex projects and quality initiatives. Expertise in certain quality areas. Lead, guide and support global TRD project teams in all quality-relevant topics, questions, and issues. Develop project strategies in alignment with TRD considering all relevant cross-functional aspects to ensure the quality of deliverables within the project. QA representative at expert panel; Lead QA aspects of new technology projects; QA representatives for complex due diligence projects. Lead PAI and submission preparations, ensure inspection site readiness.

Major Activities:

• Lead and support global TRD project team, and represent TRD QA globally in TRD 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 TRD QA strategies and goals and in compliance to cGMP guidelines and internal procedures.
• Understand and proactively manage the interactions of project related activities between TRD QA and other departments inside or outside of TRD.
• Proactively communicate overall project strategy, key issues and any other critical topics in a timely manner to the appropriate management level, to the TRD project leader and/or to any other relevant project team member(s).
• Provide input to contracts and QA agreements with third parties. Approve project-specific QA agreement amendments for assigned projects.
• Lead or participate in global and/or cross-functional initiatives.
• Prepare and guide TRD project teams for Mock-PAI and PAI in the frame of the PAI preparation process and submission preparation.

Requirements:

• Minimum: Bachelor (> 10 years’ pharma quality or operations); Desirable: 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 Drug Product/Medical Devices (combination products) manufacturing and control.
• Experience with Health Authority Inspections (FDA and EMA in particular), Notified Body inspections and knowledge of RegCMC requirements for NB, Health Authority submissions (INDs, IMPDs, NDAs, ANDAs, MAAs).
• Broad experience in combination product development as well as in Quality Assurance and/or Quality Control departments.
• Experience in Technical Operations or equivalent experience from external company is preferred.
• Proven track record in successfully supporting 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: 1 January 2027

Contract: 12 months

Why Novartis:

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?

EEO Statement:

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.

Accommodation:

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 [e-mail].