Product Development Quality (PDQ) strives for unrivaled transparency with health authorities, patients and society. Our work provides leadership, know-how and partnering on quality across molecules, Pharma affiliates and global regulated processes. We partner across Roche/Genentech to provide a quality management framework as well as actionable quality assured data to ultimately ensure that our patients are protected and the integrity of Roche/Genentech data. The key to PDQ’s success is trust, data and velocity. From non-clinical studies to post marketing pharmacovigilance to medical devices, we make sure that Roche/Genentech is doing it right, so that patients can trust.
This internship position is located in Welwyn Garden City.
The following is not an exhaustive list of responsibilities; rather the list below highlights possible activities that the successful candidate can get involved in:
Key responsibilities
Quality Assurance
- Contribute to the design and implementation of quality assurance strategies for an assigned molecule/product, process or affiliate, through partnering and engaging with relevant stakeholders, as well as execution of quality assured activities (audits) as per the strategies
- Contribute to the development, implementation, maintenance and improvement of the quality assurance infrastructure strategies to enable quality assurance teams to work effectively and efficiently
Analytics and Insights
- Contributes to the design and development of new data science solutions with the ability to identify the best approach to answer GxP quality questions
- Contribute to driving innovation for data analytics and predictive analytics within PDQ
Quality Solutions
Deliver quality solutions that enable Roche to demonstrate confidence in Roche's QMS, pipeline and marketed products. Design and develop processes, perform process improvements, regulatory intelligence and progress the NextGen QMS, Roche's QMS Framework spanning global Product Development functions, Affiliates and Research Early Development to identify, measure, control and enhance core business processes, maintain compliance and continuously improve thus ensuring patient safety and data integrity.
Program highlights
- Intensive 3 months, full time (37.5 hours per week) paid internship.
- Program start dates are in April/May 2025.
- Ownership of challenging and impactful business-critical projects.
- Work with some of the most talented people in the biotechnology industry.
- Lead or participate in intern committees to design and coordinate program events and initiatives.
- Professional & personal development curriculum throughout the program, including networking opportunities.
Who you are
Education
The successful candidate will have either recently completed (within the last two years) or working towards completing an undergraduate degree or postgraduate qualification in a medically related, life science/biological or data/computer science program.
Other skills/qualifications
- Excellent communication, collaboration, and interpersonal skills.
- Willingness/ability to manage and influence stakeholders at various levels of seniority as well as negotiate effective solutions
- Open minded and ‘out of the box’ thinking with a focus on making a valuable impact
- Complements our culture and the standards that guide our daily behavior & decisions: Integrity, Courage, and Passion.
Along with the submission of your CV, a cover letter is optional.
Relocation benefits are not available for this job posting.
