Arbeitgeber: Novartis Pharmaceutical Manufacturing GmbH

Job ID: REQ-10088285

Major Accountabilities

º Oversee production and testing activities to ensure compliance with cGxP (data integrity and eCompliance) º Review and approve QC testing results, production documentation, QC records, and AS&T records º Support exception, deviation, and investigation processes with timely follow-up and documentation º Ensure QC activities comply with GMP, GxP, regulatory, and internal quality standards º Support batch release activities in compliance with GMP, registration, and license requirements º Contribute to audit and inspection readiness (support during GxP audits and regulatory inspections) º Ensure analytical equipment qualification, calibration, and laboratory documentation º Support operational excellence and continuous improvement initiatives

Obligatory Requirements

º Education as a lab technician or equivalent qualification or university degree in a scientific/technical field (e.g., chemistry, pharmacy, biology) º Professional experience in a pharmaceutical laboratory, QC, QA, analytics, or equivalent GMP-regulated environment º Strong knowledge of GMP, GxP standards, quality control testing, quality assurance, and quality documentation º Good understanding of laboratory equipment, analytical processes, data integrity, and compliance expectations º Ability to manage ambiguity and support investigations, deviations, CAPAs, and continuous improvement activities º German language skills for flawless communication and good English skills

Rewards

º Market-competitive base salary º Attractive incentive program º Company pension scheme º Childcare facilities º Learning and development opportunities º Global career opportunities within the Novartis Group º Flexible and hybrid working options (where possible) º Minimum of 14 weeks paid parental leave

Location Austria / Schaftenau

Apply to the Job: https://www.novartis.com/at-de/careers/career-search/job/details/req-10088285-quality-control-specialist-ii-mfd-de-de