Logo for Novartis

Senior Director, Global Sterility Assurance

Role overview

Qualifications

  • Bachelor's degree in pharmacy, chemistry, microbiology, or a related scientific discipline; advanced degree preferred
  • Minimum of 10 years of experience in global, cross-disciplinary project management and leadership roles within the pharmaceutical industry
  • Extensive experience delivering sterility assurance leadership within U.S. pharmaceutical manufacturing and FDA-regulated environments
  • Deep technical expertise in microbiology, aseptic processing, and sterile manufacturing operations

Responsibilities

  • Lead sterility assurance strategy with primary focus on U.S. manufacturing and FDA regulatory expectations
  • Drive North America/U.S. inspection readiness and remediation programs, partnering with sites to prevent repeat observations
  • Serve as Global Process Owner for Sterile Operations, governing and harmonizing aseptic processes across platforms and sites
  • Provide proactive sterility assurance leadership during the design and qualification of new production facilities and microbiology laboratories

Key facts

  • Remote from: Canada
  • Full time
  • Senior (5-10 years)
  • French, English

Other skills

  • Quality Assurance
  • Quality Control
  • Business Acumen
  • Financial Acumen
  • Coaching
  • Collaboration
  • Strategic Thinking
  • Communication
  • Leadership
  • People Management

About the company

Novartis logo

Novartis

Pharmaceutical Manufacturing

Novartis is an innovative medicines company. Every day, working to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 250 million people worldwide. Find out more at https://www.novartis.com See our community guidelines: https://go.novartis.social/3Nboxki

Company details

Company typeXLarge
IndustryPharmaceutical Manufacturing
Company size10001

Your match analysis

See how your profile stacks up against this role.

We compared the job requirements to your profile to show where you're strong and where you fall short.

Job description

Job Description Summary

#LI-Remote

Location: Canada/Remote

Novartis will not offer relocation support for this role.

Are you ready to shape sterility assurance strategy with a strong North America regulatory focus while influencing manufacturing quality across the Novartis network? As the Senior Director, Global Sterility Assurance, you will set sterility assurance and aseptic processing standards with primary accountability for aligning U.S. manufacturing operations to FDA expectations. Partnering closely with senior leaders across Quality, Manufacturing, Engineering, and Technical Operations, you will drive inspection readiness, strengthen aseptic capabilities, and guide complex, cross-platform initiatives. This role blends deep technical expertise with enterprise leadership—protecting product quality, safeguarding patient supply in the U.S., and enabling consistent sterility assurance excellence globally.


 

Job Description

Key Responsibilities

  • Lead sterility assurance strategy with primary focus on U.S. manufacturing and FDA regulatory expectations.
  • Drive North America/U.S. inspection readiness and remediation programs, partnering with sites to prevent repeat observations.
  • Serve as Global Process Owner for Sterile Operations, governing and harmonizing aseptic processes across platforms and sites.
  • Provide proactive sterility assurance leadership during the design and qualification of new production facilities and microbiology laboratories, ensuring that layouts, processes, and controls meet all relevant regulatory, aseptic, and quality compliance requirements.
  • Serve as subject matter expert in microbiological topics, leading resolution of sterility and contamination escalations.
  • Lead complex, cross-functional and cross-site projects delivering U.S. sterility assurance priorities and global quality initiatives.
  • Monitor sterility assurance performance indicators and deliver clear, executive-level insights to enable timely, compliant decision-making.
  • Represent Novartis externally as a recognized sterility assurance expert, supporting U.S. industry engagement and global alignment.

Essential Requirements

  • Bachelor’s degree in pharmacy, chemistry, microbiology, or a related scientific discipline; advanced degree preferred.
  • Minimum of 10 years of experience in global, cross-disciplinary project management and leadership roles within the pharmaceutical industry, preferably in strategic Site or global QA Operations and/or Compliance roles.  Pharmaceutical production experience is indispensable.
  • Extensive experience delivering sterility assurance leadership within U.S. pharmaceutical manufacturing and FDA-regulated environments.
  • Deep technical expertise in microbiology, aseptic processing, and sterile manufacturing operations.
  • Demonstrated success leading enterprise-level quality initiatives across multiple sites and manufacturing platforms.
  • Proven ability to influence senior stakeholders, lead cross-functional teams, and drive complex, high-impact programs.
  • Travel up to 25%
  • Language : French speaking and writing: Advanced. English speaking and writing: Advanced.

At Novartis Canada, we are determined to be a valued partner and advocate, with a deep understanding of patient needs along the entire care journey – from drug development, to diagnosis, to access and beyond. Part of the way we are doing this is by leveraging data, technology, and partnerships.

Research & Development: we focus on four core therapeutic areas: Cardiovascular, Renal & Metabolic, Immunology, Neuroscience and Oncology. We also develop and deliver treatments through other promoted and established brands, which today are helping millions of patients. Over the last three years, our average annual research and development investment in Canada was over $30 million, and we conduct clinical trial research in every region throughout Canada.

Commitment to Diversity and Inclusion: Novartis is committed to building outstanding, inclusive work environment and diverse team’s representatives of the patients and communities we serve.


 

Skills Desired

Business Acumen, Change Management, Coaching, Collaboration, Communication, Continuous Improvement, Financial Acumen, Leadership, People Management, Quality Assurance (QA), Quality Compliance, Quality Management, Quality Management Systems (QMS), Risk-Based Decision Making, Risk Management, Stakeholder Management, Storytelling, Strategic Thinking

Apply once. Then go straight to the hiring manager.

After you apply, unlock the direct contact details of the people who actually make the call. A quick follow-up makes you 5x more likely to land an interview.

MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
Unlocked after you apply
·

Related jobs

Other jobs at Novartis

Premium

Reach out to the hiring manager directly.

Gain access to the contact details of the hiring managers who actually decide, and reach out to network with them directly. That, plus more when you upgrade:

  • Full match report with fit score and gaps
  • Career diagnostics on how recruiters read you
  • Curated company matches and warm intros
  • 48h early access to new roles

Cancel anytime.