At a Glance
- Tasks: Lead a global team to ensure compliance and drive quality in pharmacovigilance.
- Company: Join Johnson & Johnson, a leader in innovative healthcare solutions.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Dynamic role with leadership opportunities and a focus on innovation.
- Why this job: Make a real impact on patient safety and quality management in healthcare.
- Qualifications: Master’s degree and extensive experience in pharmaceutical compliance and medical safety.
The predicted salary is between 80000 - 100000 € per year.
Johnson & Johnson is recruiting for a Director, PV Quality Management located in Titusville, NJ, Raritan, NJ, Beerse, Belgium, High Wycombe, UK, Maidenhead, UK, Allschwil, Switzerland or Schaffhausen, Switzerland.
Overview
The Independent Medicines Quality Systems (IMQS) organization is responsible for the Innovative Medicine Quality Management Systems (QMS) and GxP process ownership. The Director, Pharmacovigilance Quality Management leads a global team of PV Quality Management experts to deliver end‑to‑end processes, qualifications and training within the IMQS‑supported QMS framework. The role ensures compliance with regulatory requirements, drives quality‑by‑design principles, and collaborates with senior leaders across R&D, Medical Safety, and global business partners.
Responsibilities
- Map, analyze, develop, and implement compliant and efficient end‑to‑end processes and related training and qualification as part of the GxP/GPvP Quality Management Framework.
- Represent IMQS‑PDM and serve as a champion to key (pre)clinical, OCMO, and Global/Local Medical Safety, Therapeutic Area, and other business partners and stakeholders.
- Act as conduit between business partners, quality groups and governance to ensure the GxP/GPvP Quality Framework evolves with the business and regulatory requirements and needs, including changes, CAPA, investigational/inspection requests.
- Implementation of the transformation roadmap of PDM towards data‑centric content and qualification management, and the internal first‑time‑right end‑to‑end process from request to effective process/qualification material.
- Lead and manage a team of PVQM experts.
- Coordinate the work of the PPQM team in a respective business unit and collaborate with business partners managing the delivery of end‑to‑end connected processes.
- Develop functional programs for PVQM staff and identify developmental needs, preparing personnel for more responsible positions and increasing effectiveness.
Other Responsibilities
- Leadership or support of projects, meetings, etc. as directed by the Head of Process and Data Management.
Independence/Autonomy
The leader acts independently and with high impact to drive results and organizational performance, seeking guidance only as needed. The leader is expected to proactively set priorities to achieve IMQS goals and objectives.
Required Minimum Education
Master’s degree in Science or Business.
Required Minimum Years of Experience
A minimum of 12 years’ experience in a medium to large scale matrix organization, including a minimum of 10 years of experience in a pharmaceutical/device compliance–related field or equivalent time and experience in a related healthcare R&D area. A minimum of 5 years’ experience in Medical Safety/Pharmacovigilance, process design, training design or related field is required.
Required Knowledge, Skills and Abilities
- Strong oral and written communication in English.
- Industriousness, self‑awareness, adaptability, attention to detail, and high teamwork capacity.
- Strong knowledge of worldwide (pre)clinical safety compliance regulations and guidelines, and broad exposure to regulatory and legal requirements within the life science industry.
- Ability to resolve complex problems within tight timelines.
- Decision‑making regarding business issues, strategic support, and organizational development as required by business urgency and growth.
- Significant collaboration, alignment and influencing across R&D Quality, OCMO, Global/Local Medical Safety, and various R&D functions.
Leadership Experience and Skills
- Strong personal leadership with demonstrated competency interfacing with senior leaders.
- Strong networking and relationship‑building skills.
- Proven track record of leading and developing people in a matrixed organizational set‑up.
- Strong organizational and people change leadership and management skills.
- Ability to create an open and inviting environment.
- Ability to embrace generational differences.
- Ability to operate in a virtual environment.
- Proven business acumen.
- Strong understanding of the digital and data science landscape.
- Exceptionally written and verbal communication skills.
Technology Experience and Skills
- Proficiency with MS365 software.
- Proficiency with Project Management software.
- Proficiency with Process Value Stream mapping and analyzing software (preferred).
Preferred Knowledge, Skills and Abilities
- Process value‑stream mapping and analysis software proficiency.
Director, PV Quality Management in Maidenhead employer: Johnson & Johnson
Johnson & Johnson is an exceptional employer, offering a dynamic work environment in the heart of innovative healthcare. With a strong commitment to employee growth, the company provides extensive training and development opportunities, fostering a culture of collaboration and excellence. Located in vibrant areas such as Titusville, NJ, and Beerse, Belgium, employees benefit from a diverse and inclusive workplace that values quality and compliance, making it an ideal place for professionals seeking meaningful and rewarding careers in pharmacovigilance.
StudySmarter Expert Advice🤫
We think this is how you could land Director, PV Quality Management in Maidenhead
✨Tip Number 1
Network like a pro! Reach out to connections in the industry, especially those who work at Johnson & Johnson or similar companies. A friendly chat can open doors and give you insider info that could help you stand out.
✨Tip Number 2
Prepare for interviews by researching the company culture and values. Johnson & Johnson is all about quality and compliance, so be ready to discuss how your experience aligns with their mission and how you can contribute to their goals.
✨Tip Number 3
Showcase your leadership skills! As a Director, you'll need to demonstrate your ability to lead teams and manage projects effectively. Share specific examples of how you've successfully led initiatives in the past during your interviews.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for passionate individuals who want to make a difference in the field of pharmacovigilance.
We think you need these skills to ace Director, PV Quality Management in Maidenhead
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter to highlight your experience in pharmacovigilance and quality management. We want to see how your skills align with the role, so don’t hold back on showcasing your relevant achievements!
Showcase Your Leadership Skills:As a Director, you'll need to demonstrate strong leadership capabilities. Use your application to share examples of how you've successfully led teams or projects in the past. We love seeing candidates who can inspire and develop others!
Be Clear and Concise:When writing your application, clarity is key! Make sure your points are easy to read and straight to the point. We appreciate well-structured applications that get to the heart of your qualifications without unnecessary fluff.
Apply Through Our Website:We encourage you to submit your application through our website for the best chance of being noticed. It’s super easy, and it helps us keep everything organised. Plus, you’ll be one step closer to joining our amazing team!
How to prepare for a job interview at Johnson & Johnson
✨Know Your Stuff
Make sure you brush up on your knowledge of pharmacovigilance and quality management systems. Familiarise yourself with the latest regulations and guidelines in the life sciences industry, as well as Johnson & Johnson's specific processes. This will show that you're not just interested in the role but are also prepared to hit the ground running.
✨Showcase Your Leadership Skills
As a Director, you'll need to demonstrate strong leadership capabilities. Prepare examples of how you've successfully led teams in a matrixed organisation, managed change, and developed talent. Highlight your ability to create an open environment and embrace generational differences, as these are key to fostering collaboration.
✨Communicate Clearly
Strong communication skills are essential for this role. Practice articulating your thoughts clearly and concisely, both verbally and in writing. Be ready to discuss complex issues and how you've resolved them in the past, as well as your approach to influencing stakeholders across various functions.
✨Prepare Questions
Interviews are a two-way street, so come prepared with insightful questions about the company's vision for the future of pharmacovigilance and quality management. Ask about the challenges they face and how you can contribute to overcoming them. This shows your genuine interest in the role and helps you assess if it's the right fit for you.
