Quality Oversight and Compliance Director in Banstead
Quality Oversight and Compliance Director

Quality Oversight and Compliance Director in Banstead

Banstead Full-Time 80000 - 100000 ÂŁ / year (est.) Home office (partial)
Pfizer, S.A. de C.V

At a Glance

  • Tasks: Lead quality oversight and compliance initiatives to ensure patient access to life-changing medicines.
  • Company: Join Pfizer, a global leader in healthcare innovation and patient care.
  • Benefits: Enjoy competitive pay, comprehensive benefits, and a hybrid work environment.
  • Other info: Collaborative culture with opportunities for professional growth and innovation.
  • Why this job: Make a real impact on global health while driving compliance and quality standards.
  • Qualifications: Strong experience in drug development and regulatory processes required.

The predicted salary is between 80000 - 100000 ÂŁ per year.

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place. To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.

Pfizer Research & Development serves as the beating heart of Pfizer's trailblazing product pipeline, the essence of our mission to bring life-changing medicines to the world. Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues. At Pfizer, we are committed to delivering medicines to the world with greater speed, without compromising on excellence and integrity.

Navigating both local and global regulations is crucial, and the dynamic regulatory landscape demands innovative thinking and meticulous attention to detail. Your unwavering dedication and specialized knowledge will play a pivotal role in broadening and hastening patient access to Pfizer's medicines and vaccines. Your role will involve interpreting federal, state, and international regulations as they apply to our products, processes, practices, and procedures. You will investigate and resolve compliance issues both within and outside of Pfizer, ensuring that our commitment to excellence and integrity remains steadfast.

The Quality Oversight and Compliance Director is responsible for developing and maintaining Quality Plans, ensuring inspection and audit readiness, providing quality oversight of process deviations, investigations and associated corrective and preventive actions, and driving compliance of pan-regulatory (e.g. Manufacturing, Regulatory Strategy, CMC, Submissions, Clinical) information and processes globally.

The Quality Oversight and Compliance Director works to instil a quality mindset by ensuring the quality and compliance of regulatory processes and product/license information through clearly defined and documented metrics, identifying data trends and addressing associated process risks in collaboration with Regulatory Process Business Process Owners (BPOs) and stakeholders.

The Quality Oversight and Compliance Director works with Regulatory Process BPOs and stakeholders to identify and investigate procedural/compliance gaps and deviations, identify root cause and establish/monitor appropriate remediation plans through timely completion. The Quality Oversight and Compliance Director supports and drives implementation of inspection readiness, audit preparedness and training compliance.

What You Will Achieve

  • Develop and lead/co-lead highly complex projects, creating mid-term plans that impact results and drive innovation.
  • Identify critical quality process parameters/KPIs to ensure data and process quality and collaborate to create associated Quality Plans and metric reports/dashboards.
  • Provide oversight of existing and input to planned processes/systems/controls to ensure that quality is built-in to enable consistent compliance.
  • Identify procedural/compliance gaps associated with in scope processes and establishes mitigation and remediation plans with BPOs that provide optimal balance of compliance and business need.
  • Drive the investigation, remediation and closeout of Quality Events and associated corrective and preventive actions.
  • Drive and support inspection readiness activities and provide remediation support for audit (or inspection) findings.
  • Identify opportunities for improvement of pan-regulatory data and business processes and procedures through the definition, management and analysis of metric data in collaboration with BPOs and other stakeholders.
  • Leverage relationships to meet the needs of various business units, serving as an advisor and influencing management decisions.
  • Make decisions in complex problems, recommend innovative solutions, and support in solving issues impacting business units.
  • Act independently on self-initiated projects, using knowledge and judgment in complex decisions within business units.
  • Guide Pfizer by interpreting regulations and designing compliance programs, conducting audits, and evaluating policies.
  • Provide expertise on quality standards, support partner functions globally, and drive risk management and quality oversight.

Minimum Requirements

  • A BA/BS with at least strong experience or an MBA/MS with strong experience or a PhD/JD with experience or an MD/DVM with some experience.
  • Profound knowledge of drug development, license maintenance processes, regulatory codes, guidance, and technologies.
  • Experience with standard tools of continuous improvement and quality investigations, including DMAIC, root cause analysis, interview techniques and human performance analysis.
  • Ability to present and articulate issues for resolution, communicating regularly with key stakeholders to ensure alignment and provide consultation as a scientific/technical resource for assigned projects.
  • Familiarity with systems and electronic technologies that support regulatory activities.
  • Ability to lead and operate seamlessly to influence colleagues across the organization and ensure delivery to time and quality driving highly complex projects to meet evolving business needs and established deadlines.
  • Ability to work effectively within or lead a team in a matrix structure.
  • Ability to influence without authority.
  • Proficiency in Microsoft Office.
  • Strong analytical and problem-solving skills.
  • Excellent written and verbal communication skills.

Preferred Requirements

  • A Master's degree (MA/MBA/MS) with over 12 years of experience or a Doctorate (PhD/PharmD/JD) with more than 9 years of experience.
  • Proficiency in Lean and/or Six Sigma methodologies.
  • Experience in engaging with the external regulatory and pharmaceutical environment.
  • A solid understanding of the business and financial landscape.
  • Strategic thinking and the ability to develop innovative solutions.
  • Experience in risk management and quality oversight.
  • Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity.
  • Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use.

Work Location Assignment: Hybrid

Quality Oversight and Compliance Director in Banstead employer: Pfizer, S.A. de C.V

At Pfizer, we are dedicated to fostering a culture of innovation and excellence, making us an exceptional employer for the Quality Oversight and Compliance Director role. Our commitment to employee growth is reflected in our comprehensive benefits package, dynamic work environment, and opportunities for professional development, all aimed at empowering our colleagues to make a meaningful impact on patients' lives. Located in a vibrant area that encourages collaboration and creativity, Pfizer offers a unique advantage for those looking to thrive in a fast-paced, mission-driven organisation.
Pfizer, S.A. de C.V

Contact Detail:

Pfizer, S.A. de C.V Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Quality Oversight and Compliance Director in Banstead

✨Tip Number 1

Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.

✨Tip Number 2

Prepare for interviews by researching the company and its culture. Understand their mission and values, especially how they align with your passion for quality oversight and compliance. This will help you stand out as a candidate who truly gets it.

✨Tip Number 3

Practice your responses to common interview questions, but keep it natural. Use the STAR method (Situation, Task, Action, Result) to structure your answers, especially when discussing your experience with regulatory processes and compliance.

✨Tip Number 4

Don’t forget to follow up after interviews! A simple thank-you email can go a long way in showing your enthusiasm for the role. And remember, apply through our website for the best chance at landing that Quality Oversight and Compliance Director position!

We think you need these skills to ace Quality Oversight and Compliance Director in Banstead

Regulatory Knowledge
Quality Oversight
Compliance Management
Project Management
Data Analysis
Root Cause Analysis
Continuous Improvement
Risk Management
Communication Skills
Stakeholder Engagement
Audit Preparedness
Inspection Readiness
Analytical Skills
Technical Aptitude
Leadership Skills

Some tips for your application 🫡

Tailor Your Application: Make sure to customise your CV and cover letter for the Quality Oversight and Compliance Director role. Highlight your relevant experience in drug development and regulatory compliance, and don’t forget to mention any specific projects that showcase your skills!

Showcase Your Skills: We want to see your analytical and problem-solving skills shine through! Use examples from your past experiences to demonstrate how you've tackled complex issues and driven quality improvements in your previous roles.

Be Clear and Concise: When writing your application, keep it clear and to the point. Use straightforward language and avoid jargon where possible. This will help us quickly understand your qualifications and fit for the role.

Apply Through Our Website: Don’t forget to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered for the position. Plus, it’s super easy to do!

How to prepare for a job interview at Pfizer, S.A. de C.V

✨Know Your Regulations

Make sure you brush up on federal, state, and international regulations relevant to the pharmaceutical industry. Being able to discuss how these regulations impact Pfizer's products and processes will show that you're not just familiar with the rules but can also navigate them effectively.

✨Showcase Your Analytical Skills

Prepare to discuss specific examples where you've used analytical skills to solve compliance issues or improve quality processes. Highlight your experience with tools like DMAIC or root cause analysis, as this will demonstrate your ability to drive innovation and maintain high standards.

✨Communicate Clearly

Practice articulating complex ideas in a straightforward manner. You’ll need to communicate regularly with key stakeholders, so being able to present issues and solutions clearly will be crucial. Consider doing mock interviews to refine your communication style.

✨Demonstrate Leadership in Compliance

Be ready to share instances where you've led projects or initiatives related to quality oversight and compliance. Discuss how you influenced colleagues and drove results, as this will highlight your ability to operate effectively within a matrix structure and lead without authority.

Quality Oversight and Compliance Director in Banstead
Pfizer, S.A. de C.V
Location: Banstead

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