Quality Governance Lead

Posted 7 Days Ago
Be an Early Applicant
Mississauga, ON, CAN
In-Office
115K-151K Annually
Senior level
Healthtech • Biotech • Pharmaceutical
The Role
Lead and implement the global Management Review of Quality (MRoQ) governance framework across manufacturing and clinical supply, coordinate review cycles, synthesize quality data for executive decision-making, standardize frameworks and tools, track governance outcomes and actions, build cross-functional governance community, and support inspection readiness with presentation-ready materials.
Summary Generated by Built In

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

At Roche, we are passionate about transforming healthcare and changing patients lives. As a global leader in pharmaceuticals and diagnostics, we focus on driving scientific excellence and delivering innovative solutions that address some of the world’s most complex medical challenges. We believe that doing now what patients need next requires a diverse, inclusive, and collaborative environment where every individual is empowered to contribute to our shared purpose. Quality is at the heart of everything we do, ensuring that our life-saving treatments meet the highest standards of safety, efficacy, and compliance across the globe.

The Opportunity

As the Global Quality Governance Lead, you will support the implementation and operational execution of the Management Review of Quality (MRoQ) governance framework within the global PT Quality organization. Your core responsibilities and impact will include:

  • Drive Governance Strategy: Define and execute the global MRoQ governance strategy, ensuring full alignment with enterprise quality objectives, business priorities, and global regulatory expectations.

  • Orchestrate Global Review Cycles: Lead the end-to-end planning, coordination, and execution of global MRoQ cycles across diverse sectors, including Internal/External Manufacturing, Investigational Medicinal Products (IMP), and Cell & Gene Therapy.

  • Facilitate Senior Decision-Making: Enable leadership and key decision-making forums by synthesizing complex quality performance data into high-quality, data-driven materials and executive-level insights.

  • Standardize Frameworks and Tools: Establish, maintain, and continuously improve standardized MRoQ frameworks, templates, and digital tools to enable scalable, efficient, and consistent execution across the network.

  • Manage Forum Outputs: Orchestrate governance review forums to ensure clear, documented outcomes, and establish robust systems for tracking accountability, actions, and risk-mitigation commitments.

  • Foster Collaboration & Community: Build and lead a highly connected, cross-functional MRoQ governance community that champions transparency, process harmonization, and a strong culture of quality.

  • Support Inspection Readiness: Act as a key delegate for MRoQ and quality governance responsibilities, providing vital support and presentation-ready documentation during regulatory inspections and internal audits.

Who you are

You are a disciplined, detail-oriented professional who thrives in a matrixed multinational environment. You bring the following qualifications, skills, and experience to the team:

  • Educational Background: You possess a Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or a related scientific discipline.

  • Industry Experience: You bring 7 years++ of dedicated experience in a Quality (GxP) environment, with specific expertise in Quality Governance, QA, or Compliance within the pharmaceutical or biotech industry.

  • Regulatory & Domain Knowledge: You maintain a strong working knowledge of GMP, GCP, and/or GDP regulations across multiple domains, such as clinical supply or commercial manufacturing.

  • Governance Expertise: You have hands-on experience supporting, coordinating, or facilitating management reviews, quality council forums, or complex multi-tiered corporate governance processes.

  • Analytical & Communication Capability: You are skilled at analyzing complex quality data and translating these insights into clear, actionable executive reporting and strategic messages.

  • Stakeholder & Matrix Collaboration: You excel at partnering cross-functionally and managing stakeholders across global sites, functions, and leadership levels to drive organizational alignment.

  • Project Management & Leadership: You possess solid project management skills, an aptitude for driving continuous improvement, and emerging leadership capabilities such as mentoring teams or leading complex workstreams.

**Relocation benefits not availabel for this position**

The expected salary range for this position based on the primary location of Mississauga is 115,328.00 and 151,368.00 of hiring range. Actual pay will be determined based on experience, qualifications, and other job-related factors as determined by the company.

We use artificial intelligence to screen, assess or select applicants for this role.

This posting is for an existing vacancy at Hoffmann-La Roche Ltd.

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.

Roche is an Equal Opportunity Employer.

Skills Required

  • Bachelor's or Master's degree in Life Sciences, Pharmacy, or related scientific discipline.
  • 7+ years of experience in a Quality (GxP) environment within pharmaceutical or biotech (Quality Governance, QA, or Compliance).
  • Working knowledge of GMP, GCP, and/or GDP regulations across clinical supply or commercial manufacturing.
  • Hands-on experience supporting, coordinating, or facilitating management reviews, quality council forums, or multi-tiered corporate governance processes.
  • Skilled at analyzing complex quality performance data and producing executive-level reporting and insights.
  • Proven ability to partner cross-functionally and manage stakeholders across global sites, functions, and leadership levels.
  • Project management skills, continuous improvement aptitude, and leadership capabilities (mentoring or leading complex workstreams).
  • Ability to support inspection readiness and provide presentation-ready documentation during regulatory inspections and internal audits.

Roche Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Roche and has not been reviewed or approved by Roche.

  • Retirement Support U.S. materials describe a 401(k) with both matching and an additional company contribution, supported by formal plan documents and true‑up features. This structure is positioned as a standout element of the total package, particularly at Genentech.
  • Leave & Time Off Breadth Time‑off provisions include substantial vacation, a year‑end shutdown, and a paid six‑week sabbatical after six years. These elements indicate a recharge‑oriented approach within the U.S. offering.
  • Healthcare Strength Company materials emphasize comprehensive medical, dental, vision, and mental‑health resources alongside well‑being programs. Benefits pages consistently highlight breadth across core health coverage elements.

Roche Insights

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The Company
Provincia de Buenos Aires
93,797 Employees
Year Founded: 1896

What We Do

Roche is a global pioneer in pharmaceuticals and diagnostics focused on advancing science to improve people’s lives. The combined strengths of pharmaceuticals and diagnostics under one roof have made Roche the leader in personalised healthcare – a strategy that aims to fit the right treatment to each patient in the best way possible. Roche is the world’s largest biotech company, with truly differentiated medicines in oncology, immunology, infectious diseases, ophthalmology and diseases of the central nervous system. Roche is also the world leader in in vitro diagnostics and tissue-based cancer diagnostics, and a frontrunner in diabetes management. Founded in 1896, Roche continues to search for better ways to prevent, diagnose and treat diseases and make a sustainable contribution to society. The company also aims to improve patient access to medical innovations by working with all relevant stakeholders. Thirty medicines developed by Roche are included in the World Health Organization Model Lists of Essential Medicines, among them life-saving antibiotics, antimalarials and cancer medicines. Roche has been recognised as the Group Leader in sustainability within the Pharmaceuticals, Biotechnology & Life Sciences Industry ten years in a row by the Dow Jones Sustainability Indices (DJSI).

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