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- Tasks: Lead pharmacovigilance activities and ensure safety compliance for Sandoz products.
- Company: Sandoz is a global leader in sustainable biosimilar and generic medicines.
- Benefits: Enjoy competitive salary, annual bonus, flexible working, and 24 days leave.
- Why this job: Shape the future of healthcare while working in a diverse and inclusive environment.
- Qualifications: 10+ years in drug safety with leadership experience; healthcare qualification required.
- Other info: Join a collaborative culture that supports personal growth and impactful careers.
The predicted salary is between 43200 - 72000 £ per year.
Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and ambitious path, unique opportunities will present themselves, both professionally and personally. Join us, the future is ours to shape!
Your Key Responsibilities:
- UK National PV point of contact
- Act as the National Contact Person for Pharmacovigilance
- Collaborate and work with the UK-QPPV
- Leadership and Influence:
- Lead and oversee pharmacovigilance activities within the local Affiliate.
- Advocate for local Affiliate’s needs at local, regional, and global levels.
- Promote a comprehensive understanding of the PV system within the organization.
- Ensure adherence to local safety requirements.
- Represent the local Affiliate(s) in cross-functional and global-regional-local frameworks.
- Drive the integration of safety procedures within the organization.
- Establish strong partnership with the local Affiliate leadership and ensure exchange of key pharmacovigilance topics.
- Externally influence the local regulatory environment by participating in key local pharmacovigilance associations.
- Line management accountability and operational leadership of affiliate Patient Safety Staff.
- Facilitate efficient exchange of safety-related information within the Affiliate and within the PS organization (UK-QPPV, Patient Safety Regional Lead).
- Collaborate with local business partners, Patient Safety regional leads, QPPV, and third-party vendors.
- Stay informed about Sandoz product safety profiles.
- Support launches of Sandoz products in the territory by providing pharmacovigilance expertise during all phases of product development.
- Communicate with the local Health Authority as appropriate.
- Provide safety expertise for marketed and investigational products.
- Support risk management plans and additional risk minimization measures (aRMMs) implementation.
- Develop, implement and maintain oversight mechanisms for safety related activities conducted in the Affiliate and keep the compliance.
- Ensure compliance with local pharmacovigilance laws and quality standards.
- Contribute to the local quality management system.
- Contribute to maintenance of the local UK PSMF (PV System Master File).
- Engage in training, records management, and regulatory intelligence.
- Ensure audit and inspection readiness.
- Host and lead local inspections and audits.
What you’ll bring to the role:
- Professional qualification in Health Care Sciences (e.g., Medical Doctor, Pharmacist, Nurse)/ Master's Degree or Equivalent.
- Minimum 10 years in drug safety or pharmacovigilance with 3 years of demonstrated leadership.
- Excellent communication skills in English. Knowledge of other languages is desirable.
- Extensive understanding of local pharmacovigilance requirements, with the ability to address complex regulatory issues.
- Proficient in pharmacovigilance processes, including compliance, databases, procedures, quality assurance, and training.
- Proven ability to critically evaluate and integrate data from diverse areas/domains.
- Effective communication skills with various stakeholders.
- Experience in pharmacovigilance audits and inspections.
- Demonstrated ability for innovative and strategic thinking.
- Strong planning, negotiation, organizational, and interpersonal skills.
- Proficiency in computer and IT systems.
You’ll receive:
- Competitive salary
- Annual bonus
- Pension scheme
- Health insurance
- 24 days annual leave
- Flexible working arrangements
- Employee recognition scheme
- Learning and development opportunities
Why Sandoz?
Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, provided more than 900 million patient treatments across 100+ countries in 2024 and while we are proud of this achievement, we have an ambition to do more! With investments in new development capabilities, production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably. Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is supported! Join us!
Commitment to Diversity & Inclusion: We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Join our Sandoz Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Sandoz and our career opportunities, join the Network here: Sandoz Talentpool (novartis.com)
Senior Patient Safety Manager employer: Sandoz UK & Ireland
Contact Detail:
Sandoz UK & Ireland Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Patient Safety Manager
✨Tip Number 1
Familiarise yourself with the latest pharmacovigilance regulations and guidelines in the UK. This knowledge will not only help you understand the role better but also demonstrate your commitment to staying updated in a rapidly evolving field.
✨Tip Number 2
Network with professionals in the pharmacovigilance community, especially those who have experience in leadership roles. Engaging with industry peers can provide valuable insights and may even lead to referrals or recommendations.
✨Tip Number 3
Prepare to discuss your leadership experiences in detail during interviews. Be ready to share specific examples of how you've successfully managed teams and influenced safety practices in previous roles.
✨Tip Number 4
Showcase your ability to collaborate across functions by highlighting any past experiences where you worked with diverse teams. This is crucial for the role, as it involves liaising with various stakeholders within and outside the organisation.
We think you need these skills to ace Senior Patient Safety Manager
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in pharmacovigilance and leadership roles. Use keywords from the job description to demonstrate that you meet the essential requirements.
Craft a Compelling Cover Letter: In your cover letter, express your passion for patient safety and how your background aligns with Sandoz's mission. Mention specific experiences that showcase your ability to lead and influence within pharmacovigilance.
Showcase Communication Skills: Since excellent communication skills are essential for this role, provide examples in your application of how you've effectively communicated with various stakeholders in previous positions.
Highlight Regulatory Knowledge: Emphasise your understanding of local pharmacovigilance requirements and any experience you have with audits and inspections. This will demonstrate your capability to navigate complex regulatory issues.
How to prepare for a job interview at Sandoz UK & Ireland
✨Understand the Role Thoroughly
Before your interview, make sure you have a solid grasp of the responsibilities outlined in the job description. Familiarise yourself with pharmacovigilance processes and Sandoz's specific products to demonstrate your expertise and readiness for the role.
✨Showcase Leadership Experience
As this position requires leadership skills, prepare examples from your past experiences where you successfully led teams or projects. Highlight your ability to influence and advocate for your team's needs, as well as how you've navigated complex regulatory environments.
✨Prepare for Technical Questions
Expect to be asked about your knowledge of local pharmacovigilance laws and quality standards. Brush up on relevant regulations and be ready to discuss how you've ensured compliance in previous roles, as well as your approach to audits and inspections.
✨Demonstrate Effective Communication Skills
Since the role involves collaboration with various stakeholders, practice articulating your thoughts clearly and concisely. Be prepared to discuss how you've effectively communicated safety-related information in the past and how you would approach communication in this new role.