Associate Director - Analytical Project Lead Medical Devices (m/f/d)

Novartis; Österreich; Hybride; EUR 71 000 - 86 000; Plein temps

Avantages offerts par ce poste

Incentive program

Company pension

Childcare facilities

Learning opportunities

Worldwide career possibilities

Résumé du poste

Novartis in Schaftenau, Austria seeks a Senior Expert - Medical Device Analytical Representative to lead the creation of robust analytical data-packages for drug-device combination products. You will be a key contact within the global CMC analytical and device subteams, coordinating tasks from component level to final product for injectables in prefilled syringes and autoinjectors.

The role emphasizes ownership of analytical methods and validation, external collaboration with CROs, and shaping

Qualifications

• Master or PhD in engineering or chemical/bio analytics with 5+ years in parenteral combination product development.
• Proven leadership in global matrix development projects; knowledge of cGMP and ISOs.
• Fluent in English (written and spoken).

Responsabilités

• Coordinate and lead analytical tasks for drug-device combination products across components to final product.
• Select testing laboratories and manage outsourced analytical activities and CROs.
• Own analytical methods and parameter sheets for functional attributes like activation and injection force.
• Contribute to CMC strategies, documents, and regulation-ready reports; support product registrations.

Connaissances

Combination product development

Project leadership

English proficiency

Formation

Master’s or PhD in engineering or chemical/bio analytics

Outils

Minitab

Description du poste

Summary

With the increasing diversity of Novartis' portfolio, the need for drug-device combination product analytical data packages is also increasing. As such, we are searching for a Senior Expert - Medical Device Analytical Representative with combination product development experience to lead the creation of strong analytical data-packages. As a member of the global Chemistry Manufacturing Control (CMC) analytical sub team and device sub team for your project(s) you will be the main contact & coordinator for all project-specific analytical tasks related to functional attributes of drug-device combination products at all levels (from component to drug product to final product), especially for injectables like Biologics, Ribonucleic Acids, Radio-Ligands (peptides) in e.g. a prefilled syringe in a autoinjector or needle-safety-device.

Location - Schaftenau, Austria

Key Responsibilities

• As a member of global CMC analytical subteam and device subteam for your project(s), you are the contact person & coordinator for all project-specific analytical tasks related to functional/mechanical attributes of drug-device combination products at all levels (from component to drug product to final product); plan resource & budget for your project(s).
• Select testing laboratory inline with resource availability, capability and in/outsourcing strategy, e.g. GDPD, QC, CRO; lead outsourced analytical project activities at CROs and contribute to manage external partnership.
• Own drug-specific analytical methods (AMs) / parameter sheets (PSs) for functional attributes like activation and injection force, time, volume, sound, as well as (needle) safety features, organize and align x-functional inputs (e.g. with Device/Pack Tech); define, organize, document AM/PS validation and transfer.
• Co-shape and co-author x-functional analytical CMC strategies and documents, e.g. drug product and final product stability strategy, protocols and reports, method validation and transfer status summaries, Analytical Specifications (AS); organize input to Justification of Specification JoS (from Device/PackTech and HFE).
• Contribute to and review regulatory documents, support product registrations with a minimal support by Leader or assigned to moderately complex projects.
• Performs statistical data analysis using statistical tools (e.g. Minitab) to generate and justify device related specifications for clinical and commercial setup.

Essential Requirements

• Master or PhD in engineering or chemical/bio analytics or equivalent and minimum 5 years’ experience and strong knowledge in (parenteral) Combination Product Development or related area (e.g. Manufacturing, Regulatory, QA)
• Proven knowledge in late phase parenteral analytical development; leadership experience in managing development projects, ideally in a global matrix environment, understanding and awareness of regulatory guidelines for combination. product analytics, experience with cGMP and relevant ISOs
• Collaborative spirit, self-driven attitude, high level of learning agility.
• Proficiency in English (written and spoken).

Rewards

In addition to a market-competitive base salary, we offer an attractive incentive program, a modern company pension scheme, childcare facilities, learning and development opportunities as well as worldwide career possibilities within the Novartis group. In accordance with Austrian law, we are obliged to disclose the minimum salary as stated in the collective bargaining agreement. For this position the minimum salary is € 78,383.90 EUR/year (on a full-time basis). The actual salary will be significantly higher, as we strive to maintain a competitive position in the market and consider your previous experience, qualifications and individual competencies.

We are open for part-time and job-sharing models and support flexible and remote working where possible.

Commitment To Diversity And Inclusion / EEO Paragraph

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

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 [e-mail] 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.

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? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards:

Learn about all the ways we’ll help you thrive personally and professionally.

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Read our handbook (PDF 30 MB)