Regulatory Affairs Manager/Senior Manager, CMC

Job Description Summary

#LI-Hybrid (12 days per month on-site)
Office Location: Schaftenau, Austria

Novartis are seeking a Manager/Senior Manager to be responsible for regulatory activities related to Chemistry, Manufacturing and Controls (CMC), including the preparation and publication of CMC regulatory documentation for Health Authority submissions. The role also involves engaging with Health Authorities on CMC‑related questions to support both new product launches and post‑marketing activities.

 

Job Description

Major Accountabilities:

• Formulate, lead and drive global CMC regulatory strategy with a focus on innovation, balancing business benefit with regulatory compliance.

• Lead and implement global CMC submission activities (planning, authoring, reviewing, coordination, submission) for assigned projects/products.

• Identify the required documentation and any content, quality and/or timelines issues for global submissions and negotiate the delivery of approved technical source documents in accordance with project timelines.

• Author and/or review high-quality CMC documentation for HA submission, applying agreed CMC global regulatory strategies, current regulatory trends and guidelines. Ensure technical congruency and regulatory compliance, meeting agreed upon timelines and e-publishing requirements.

• Proactively communicate CMC regulatory strategies, risks and key issues throughout the life cycle in a timely manner to project teams and other stakeholders. Represent department in cross-functional project teams.

• Lead, prepare and communicate CMC risk management assessments and lessons learned on major submissions.

• Initiate and lead Health Authority interactions and negotiations.

Essential Requirements:

• Science degree (e.g. Chemistry, Pharmacy, Biochemistry, Molecular Biology, Biotechnology, Biology) or equivalent.

• Minimum 5 years of regulatory CMC experience and/or pharmaceutical industry experience.

• Demonstrated knowledge/experience in regulatory submission and approval processes and ability to deal with complex CMC regulatory issues and requirements.

• Proven ability to critically evaluate data from a broad range of scientific disciplines.

Benefits & Reward:

In addition to a market-competitive base salary, we offer an attractive incentive program, a modern company pension scheme, childcare facilities, learning and development options as well as worldwide career opportunities 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).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.

 

Skills Desired