Senior Group Director, Technical Regulatory Affairs — Roche
CHF 85'500 - 129'500
Roche · Basel (BS)
- Location
- Basel
- Contract
- full-time
- Posted
- 16 days ago
SalaryCHF 85'500 - 129'500
Role overview
At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
- At Roche you can show up as yourself, embraced for the unique qualities you bring.
- Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
- Education Master’s Degree in life science disciplines is preferred;
- Post Graduate Degree is a plus. Experience
Key requirements
- Education Master’s Degree in life science disciplines is preferred;
- Post Graduate Degree is a plus. Experience
- 8 or more years work experience in the pharmaceutical, biotechnology or related industry and CMC, quality, regulatory or related experience. Previous People management o
Application process
- Regularly follow up and check in the progress of every specific project in the team, enlighten the team to work out submission strategies for different applications and identify regulatory risks and develop migration plans.
- Build and maintain a healthy relationships with internal & external key stakeholders, like NMPA, CDE, NIFDC, Supply Chain, Quality and compliance, PDR China and PTR global,
- Collaborate with internal key stakeholders for development and alignment of technical strategy, maximizing and balancing regulatory and supply needs in China.
Additional details
- Makes decisions based on cross-functional priorities rather than functional area priorities. Project People Leader
- QUALIFICATIONS Education Master’s Degree in life science disciplines is preferred;
- Post Graduate Degree is a plus.
- 8 or more years work experience in the pharmaceutical, biotechnology or related industry and CMC, quality, regulatory or related experience. Previous People management o
Notes and original content
- Makes decisions based on cross-functional priorities rather than functional area priorities.
- Project People Leader
- Experience
- 8 or more years work experience in the pharmaceutical, biotechnology or related industry and CMC, quality, regulatory or related experience.
- Previous People management o
