regulatory affairs manager (cmc).

• hybrid model of work for flexibility and convenience,
• company car to support your mobility needs,
• comprehensive private medical care and life insurance for you and your family,
• a robust company pension plan to secure your future,
• reimbursement for sports activities and access to well-being programs to promote a healthy lifestyle,
• annual bonus recognizing your contributions and achievements,
• beneficial leave policies to support your personal and professional needs.

• Participates as the Regulatory CMC Lead on CMC/VST Teams and represents Global CMC Regulatory Affairs by providing regulatory expertise and input to team recommendations to facilitate successful product development globally.
• Actively participates on Global Regulatory Team(s) to develop global submission plans that comply with local regulatory requirements and commitments.
• Develop and execute global CMC regulatory strategy. 
• Leads the preparation of regulatory dossiers for submission to Health Authorities.
• Develop and get buy-in on regulatory CMC strategy for Health Authority responses as needed.
• May participate in selected initiatives within CMC RA / GRA.
• Participates in and conducts due diligence/licensing evaluations as needed.
• Drives a culture of continuous improvement and communicates critical issues.
• Ensures the CMC development and commercial product regulatory strategy meets global regulatory requirements. 
• Assures connectivity to the overall global regulatory strategy through partnership and communication with other departments.
• Refines regulatory strategies as new data become available.
• Develop and update contingency plans for issues that may affect registration, regulatory compliance and the continued lifecycle management of the products in scope. 
• Effectively and tactfully communicates with health authorities; maintain good rapport and credibility.
• Reviews CMC regulatory dossiers for global submissions throughout the product lifecycle.
• Provides accurate regulatory assessments of chemistry, manufacturing and control changes to teams/projects and executes regulatory planning and implementation.

• BS in biological, pharmaceutical, chemical or engineering sciences with generally a minimum of 8+ years of experience inclusive of post graduate education and/or pharmaceutical or health care industry experience or equivalent. 
• Proficiency in English (min. C1).
• Demonstrated ability to communicate regulatory requirements.
• Solid understanding of biology, chemistry and/or engineering relevant to pharmaceutical industry 
• Experience developing regulatory strategies and an understanding of product development, seen as an expert on product development and how it is applied in global regulatory strategy.
• Strong attention to detail with high-level verbal and written communication skills 
• Communicates cross-functionally and cross-company. Presents and defends CMC management-approved regulatory strategy and opinion to project teams.
• Demonstrates model behavior that understands what the priorities are and encourages others to drive for results
• Experience interacting with Health Authorities under supervision of a senior member of the CMC RA staff. 
• Good knowledge of global HA laws, regulations, guidance and regulation submission routes available for assigned products.
• Some understanding of competitors in the area and what they are doing in early/late development 

Employment agency entry number 47

this job offer is intended for people over 18 years of age