AS&T Expert

Novartis; Österreich; Vor Ort; EUR 59.044 - 72.165; Vollzeit

Zusammenfassung

Novartis is seeking an Analytical Science and Technology (AS&T) Expert in Austria to coordinate and lead analytical activities for customer projects and internal innovations. You will provide scientific expertise, manage method transfers, and ensure compliance with regulatory requirements.

The role requires a university degree in a natural science or related field and about 3–5 years’ pharma/analytical GMP experience, with fluency in English and German.

Qualifikationen

• University degree or FH in natural science/technical field or equivalent
• 3–5 years’ experience in pharma/analytical GMP environment
• Fluent in English and German

Aufgaben

• Coordinate and manage analytical activities across projects
• Oversee analytical method transfers and stability studies
• Present analytical data to local and international project teams
• Ensure lifecycle management of analytical methods and compliance with pharmacopoeia and health authorities
• Handle deviations/investigations and change control
• Serve as point of contact for health authorities and audits/inspections
• Collaborate with Manufacturing, analytical development, production, QA and regulatory teams
• Compile and review analytical protocols, reports, and process verification documents
• Budget external analytical activities and manage reference substances and control samples

Kenntnisse

English

German

Ausbildung

University degree or FH in natural science/technical background

Tools

MS Office

Jobbeschreibung

About The Role

The Analytical Science and Technology (AS&T) Expert is responsible for coordinating and managing analytical activities across products, including both customer‑related projects and innovative Novartis initiatives, and for providing scientific analytical expertise and support.

Major Accountabilities

• Management and oversight of all analytical activities related within responsible projects
• Coordination and management of analytical method transfers and stability studies
• Presentation and discussion of analytical data in local and international project teams. Life‑cycle management of analytical methods, including control of method performance, analytical method validation, pharmacopoeia and health authority compliance and definition of method improvements
• Handling of deviations, investigation, OOS/OOE/OOT cases as well as changes and complaints
• Person of contact for analytical questions from health authorities and analytical subject matter expert during audits and inspections
• Cross‑functional interface with Manufacturing Science & Technology team, analytical development, production, quality assurance and regulatory department
• Implementation of GMP requirements. Compilation and Review of documents (analytical protocols and reports, annual performance quality reports, ongoing process verification reports, registration documents)
• Budgeting and cost control of external analytical activities
• Management of reference substances and control samples

Minimum Requirements

• University degree or FH with natural science/technical background (e.g. chemistry, pharmacy, biology) or equivalent education.
• Approx. 3 to 5 years in pharmaceutical industry and/or analytical laboratory in GMP environment. MS Office- and other standard IT applications.
• Fluent in English and German.

Rewards

You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-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 €65,605.54/year (on a full time basis). We also offer a potential market oriented excess payment in line with your experience and qualifications.

The 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. Further details will be provided during the application process.

Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics.

Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.

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.