Job description


  • Entry level
  • No Education
  • Salary to negotiate


Thank you for taking an interest in Global Regulatory at Roche. If you are interesting in working with us in the future please apply to this talent pool. We will keep your details and be in touch with you about future and current opportunities.
Therefore please add a cover letter with your CV explaining:
why you want to join roche
what area(s) of Global Regulatory you are interested in and why and
why Roche
Whilst in this Talent Pool you are not applying directly to a specific role so please continue to have a look at the various opportunities we have within Regulatory HERE
Please also feel free to reach out to Fiona Mcfarlane ( who is the Talent Acquisition Specialist for Regulatory.
Global Regulatory Programme Management
We work with cross functional global teams bringing new medicines from entry-into-human studies through to licensure and post marketing in Europe, USA, China and markets worldwide. 
Roles range from entry level graduate trainees to senior roles with global product and portfolio accountability. As your experience and leadership skills grow, Roche offers you the opportunity to grow your career.  
From the Roche Welwyn development site in the UK, you will work with colleagues around the world, in other development sites in Switzerland, the US, Canada, China and Japan as well as with local regulatory colleagues in our affiliate offices.
Example Roles in the UK
Global Regulatory Leader:  A key role, accountable for the global regulatory strategy and deliverables for a molecule. This person is the senior regulatory representative on global development teams and leads the regulatory affairs sub team.
EU partners:  With roles from entry level associate to principal partners taking increasing responsibility to lead and drive the regulatory strategy and deliverables for the EU. Working closely with global regulatory leads, other regulatory colleagues and cross functional teams you could be working on a NME filing, a line extension, supporting post marketing activities or early development projects.

Regulatory Documentation
Global Documentation is responsible for preparing regulatory documents to meet the evolving needs of Health Authorities using our expertise in writing, science and regulatory requirements.​ We have staff located in Basel, Welwyn, Mississauga and San Francisco.
Our global team of regulatory documentation scientists work with multiple departments throughout the organization providing end to end support of regulatory documents supporting the development and/or maintenance of our product licenses worldwide. 
Example Roles in the UK
Entry level graduate trainees and associates support activities e.g preparation of clinical and safety documents such as DSURs, IBs, CSRs for submission to Health Authorities, 
Functional managers provide direction and leadership to regulatory documentation scientists and functional expertise to initiatives and activities across Roche 
Team Leaders lead a global matrix team of documentation scientists and providing strategic oversight for the preparation of clinical and safety documents within a therapeutic area or within a particular stage of development.

Global Regulatory Labeling
Our vision is to ensure consistent and safe use of medicines in the global health care environment through the development of high quality labels.​ We maintain and develop the global company core datasheet and have staff located in  Roche’s global development sites in Basel, Welwyn, Mississauga and San Francisco. 
As a member of our team in Welwyn, you can build bridges globally through interactions with local regulatory affiliates (90+ countries) and other Roche international development sites.
As your experience grows there are opportunities to mentor junior team members and lead department initiatives.

Example Role in the UK
As the labelling strategist you will be creating core data sheets for innovative medicines that directly support healthcare professionals with their clinical decision-making.  You have the opportunity to engage with expert multi-function project teams throughout the clinical development and commercial lifecycle of first/best in class medicines.  Using your strategic labelling knowledge you drive the development of the core data sheet mapping out labelling risks and opportunities.
Regulatory Business Office
The Regulatory Business Office comprises a diverse group of functions providing support, guidance and framework

About the company

Roche is a Swiss global health-care company that operates worldwide under two divisions: Pharmaceuticals and Diagnostics. Its holding company, Roche Holding AG, has bearer shares listed on the SIX Swiss Exchange.

The company headquarters are located in Basel and the company has many pharmaceutical and diagnostic sites around the world – including: Tucson, AZ; Pleasanton, CA; Vacaville, California, Oceanside, California, Branchburg, NJ; Indianapolis, Indiana; Florence, South Carolina; and Ponce, Puerto Rico in the US; Welwyn Garden City and Burgess Hill in the UK; Clarecastle in Ireland; Mannheim and Penzberg in Germany; Mississauga and Laval in Canada; Shanghai in China; Mumbai & Hyderabad in India; São Paulo and Rio de Janeiro, Brazil; Segrate, Milan in Italy; Johannesburg in South Africa; Karachi, Islamabad and Lahore in Pakistan. There are 26 manufacturing sites worldwide.

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