At a Glance
- Tasks: Lead the design and maintenance of safety processes in pharmacovigilance.
- Company: Roche is a global leader in healthcare, dedicated to innovation and patient safety.
- Benefits: Enjoy a diverse workplace, flexible working options, and opportunities for personal growth.
- Why this job: Make a real impact on global health while collaborating with passionate professionals.
- Qualifications: Degree in life sciences or engineering; experience in pharmacovigilance preferred.
- Other info: Join a culture that values diversity and encourages you to be your authentic self.
The predicted salary is between 43200 - 72000 £ per year.
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. Join Roche, where every voice matters.
The Position
A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.
The Safety Development and Processes team is at the heart of our Safety Risk Management function, ensuring that Roche can deliver effective scientific safety activities globally. We are an influential team dedicated to continuous improvement and innovation, and we are looking for a highly skilled and strategic leader to join us.
As a PV Process Director , you will provide expert guidance to design, develop, and maintain core safety processes for one or more areas, such as ICSR management, signal management, aggregate reporting, risk management and device incident reporting. This is a key enabling and strategic role that is instrumental in ensuring that Roche remains a leader in patient safety.
The Opportunity
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Leading the design, development, and maintenance of core safety processes, ensuring they are effective and in line with regulatory and stakeholder requirements.
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Acting as the principal subject matter expert for your assigned processes, collaborating closely with senior stakeholders and governance bodies like the EU QPPV and Medical Device Compliance Council.
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Identifying and promoting good practices and innovations, utilising process-improvement methodologies to ensure consistency and alignment across the organisation.
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Influencing external policy by participating in expert working groups and industry associations and promoting Roche activities at scientific conferences.
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Defining critical process requirements for the development of associated tools and technologies, partnering with internal and external IT teams.
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Providing leadership and subject matter expertise to continuous improvement activities and project prioritisation.
Who you are
You are a strategic thinker with a proven ability to lead and influence across a complex, global organisation. You possess a strong understanding of pharmacovigilance and device vigilance, and you are passionate about driving continuous improvement.
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A degree in a life science, healthcare, or engineering discipline (e.g., MD, PharmD, nursing, biomedical engineering), or equivalent.
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Solid relevant experience in pharmacovigilance, device vigilance, or a medical safety-related role.
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Experience in project management and/or business process improvement is preferred, as is an advanced qualification in a relevant discipline.
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Excellent written and verbal communication skills with the ability to influence broad stakeholder groups.
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The ability to operate effectively in and lead multi-functional matrix teams.
This role is based onsite at our Welwyn, United Kingdom site . We look forward to your application!
Who we are
A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let’s build a healthier future, together.
The statements herein are intended to describe the general nature and level of work being performed by employees, and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of Roche Products Ltd. At Roche Products we believe diversity drives innovation and we are committed to building a diverse and flexible working environment. All qualified applicants will receive consideration for employment without regard to race, religion or belief, sex, gender reassignment, sexual orientation, marriage and civil partnership, pregnancy and maternity, disability or age. We recognise the importance of flexible working and will review all applicants’ requests with care. At Roche difference is valued and we are proud to be an equal opportunity employer where you are encouraged to bring your whole self to work.
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PV Process Director employer: F. Hoffmann-La Roche Gruppe
Contact Detail:
F. Hoffmann-La Roche Gruppe Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land PV Process Director
✨Tip Number 1
Familiarise yourself with Roche's core values and mission. Understanding their commitment to innovation and patient safety will help you align your responses during interviews, showcasing how your experience in pharmacovigilance can contribute to their goals.
✨Tip Number 2
Network with current or former Roche employees on platforms like LinkedIn. Engaging in conversations about their experiences can provide valuable insights into the company culture and expectations for the PV Process Director role.
✨Tip Number 3
Stay updated on the latest trends and regulations in pharmacovigilance and device vigilance. Being knowledgeable about current industry standards will demonstrate your expertise and readiness to lead in this strategic role.
✨Tip Number 4
Prepare to discuss specific examples of how you've driven process improvements in previous roles. Highlighting your project management skills and ability to influence stakeholders will be crucial in showcasing your fit for the position.
We think you need these skills to ace PV Process Director
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the PV Process Director position. Tailor your application to highlight how your skills and experiences align with Roche's needs.
Craft a Compelling CV: Your CV should clearly showcase your relevant experience in pharmacovigilance and project management. Use specific examples to demonstrate your leadership abilities and strategic thinking, as these are key attributes for this role.
Write a Strong Cover Letter: In your cover letter, express your passion for healthcare and innovation. Highlight your understanding of safety processes and your ability to influence stakeholders. Make it personal and show how you can contribute to Roche's mission.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or typos. A polished application reflects your attention to detail and professionalism, which are crucial in a role that involves regulatory compliance.
How to prepare for a job interview at F. Hoffmann-La Roche Gruppe
✨Show Your Passion for Patient Safety
Make sure to express your genuine interest in patient safety and how it aligns with Roche's mission. Share specific examples from your past experiences that demonstrate your commitment to improving safety processes.
✨Demonstrate Strategic Thinking
Prepare to discuss how you approach strategic decision-making. Highlight instances where you've successfully led initiatives or influenced stakeholders in a complex environment, showcasing your ability to think critically and strategically.
✨Familiarise Yourself with Regulatory Requirements
Brush up on the latest regulations and guidelines related to pharmacovigilance and device vigilance. Being knowledgeable about these will help you answer questions confidently and show that you are well-prepared for the role.
✨Prepare for Collaborative Scenarios
Since the role involves working with multi-functional teams, be ready to discuss your experience in collaboration. Think of examples where you've successfully worked with diverse groups to achieve common goals, and how you navigated any challenges.