Descripción de la oferta
Descripción del trabajo
Job Description Summary
As a Quality Team Leader QC (m / f / d), you’ll (co-)lead a dedicated laboratory team ensuring the highest quality standards across e.g. primary / secondary packaging material testing, medical device testing and FDF release testing. You’ll combine scientific expertise with strong leadership to secure compliance, support audits, and drive continuous improvement — helping deliver safe, high-quality medicines to patients worldwide.
Key Responsibilities
Lead and develop a Quality Control team to ensure smooth daily operations and compliance with cGxP standards.
Oversee testing of packaging materials, medical devices and FDF (final dosage form) to ensure results meet quality and regulatory requirements.
Ensure timely review, approval, and release of analytical data and laboratory documentation.
Support internal and external audits and ensure prompt completion of audit actions to root‑cause level.
Maintain up‑to‑date analytical methods, SOPs, and procedures in accordance with corporate and health authority standards.
Ensure qualification, calibration, and maintenance of laboratory equipment.
Lead investigations of deviations, OOX, and complaints; define and implement effective CAPAs.
Drive continuous improvement and operational excellence initiatives within the QC function.
Manage training, performance, and development of team members in alignment with cGxP requirements.
Foster collaboration across departments and ensure a culture of quality, safety, and compliance.
Essential Requirements
University degree in natural sciences or a related technical field (e.g. chemistry, pharmacy, biology) or equivalent education with working experience.
Minimum 5 years of experience in Quality Control, Quality Assurance, or Production within the pharmaceutical industry.
Proven leadership experience in managing laboratory teams and operations.
Strong understanding of cGxP principles, analytical methods, and regulatory requirements.
Experience in deviation management, CAPA implementation, and audit preparation or support.
Excellent communication and stakeholder management skills across functions.
Solid knowledge of IT systems and laboratory applications used in QC environments.
Fluent in German and English (spoken and written).
Desirable Requirements
Experience in medical device testing and packaging material testing.
Experience in visual inspection (AQL).
Experience in analytical method transfer projects.
Familiarity with Lean or Operational Excellence initiatives within a GMP environment.
Experience in change management.
Experience in managing budgets and resources.
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 €78,383.90 / 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
Dealing With Ambiguity
Decision Making Skills
Industry Standards
Laboratory Equipment
Laboratory Excellence
Managing Resources
Organizational Savvy
Quality Control (Qc) Testing
Quality Control Sampling
Self-AwarenessSmart Risk Taking
Technological Expertise
Total Quality Management
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