AS&T Expert (m/f/d)

Reposted 2 Days Ago
Be an Early Applicant
Schaftenau, Langkampfen, Kufstein, Tirol
In-Office
64K-64K Annually
Expert/Leader
Biotech • Pharmaceutical
The Role
As an AS&T Expert, you will manage analytical aspects of drug substance and product stewardship, ensuring compliance with cGMP, overseeing method transfers and validations, and acting as a subject-matter expert during audits.
Summary Generated by Built In

Job Description Summary

#LI-Hybrid
Location: Schaftenau, Austria
Shape the future of medicines as an AS&T Expert! You’ll be responsible for managing analytical aspects with focus on drug substance and drug product stewardship with focus on technical and analytical method transfer within responsible projects to ensure that the operational business is in compliance with cGMP (Current Good Manufacturing Practices). In addition, you will ensure analytical Life Cycle Management for commercial products and drive quality across projects—making a real impact on patient safety and product excellence.


 

Job Description

Key Responsibilities

  • Lead and oversee all analytical activities within assigned projects
  • Manage lifecycle of analytical methods, ensuring compliance and performance improvements
  • Execute timely method transfers and validations for new or transfer projects
  • Set up and monitor stability studies to maintain product quality
  • Act as primary contact for internal teams, external partners, and contract labs
  • Provide scientific support for Quality Control, Production, and Regulatory submissions
  • Serve as subject-matter expert during audits and health authority inspections

Essential Requirements

  • PhD in a scientific or technical field (e.g., pharmaceutical sciences, chemistry, pharmacy) or a Master’s degree with substantial relevant experience
  • Proven experience in the pharmaceutical industry or analytical laboratory within a GMP environment
  • Strong knowledge of analytical methods and lifecycle management
  • Ability to collaborate effectively across functions and with external partners
  • Excellent problem-solving skills with a focus on quality and compliance
  • Proficiency in German and English, both written and spoken

You’ll receive:

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 €64.023,54/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.

Commitment to Diversity and Inclusion:

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


 

Skills Desired

Continued Learning, Employee Performance Evaluations, Gmp Procedures, Managing Ambiguity, People Management, Qa (Quality Assurance), Quality Control (Qc) Testing, Quality Standards, Self-Awareness, Technical Knowledge, Technological Intelligence

Top Skills

Analytical Methods
Cgmp
Drug Development
Pharmaceutical Sciences
Quality Control
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The Company
HQ: Basel
110,000 Employees
Year Founded: 1996

What We Do

Novartis is an innovative medicines company. Every day, working to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 250 million people worldwide.

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