Roche

GxP Supplier Manager

Roche$115K — $151K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • 10+ years industry experience with external suppliers
  • Bachelor's degree in life sciences or related field
  • Expertise in supplier quality management and compliance
  • Familiarity with cGMP, ISO standards, and international regulations
  • Excellent communication skills in English
  • Proficient in Microsoft Office or Google Suite
  • Willingness to travel up to 10% for audits

Responsibilities

  • Oversee quality activities from supplier selection to decommissioning
  • Create and manage Quality Agreements with external partners
  • Manage product release quality functions, ensuring cGMP compliance
  • Collaborate with suppliers to maintain validated processes
  • Develop quality risk management plans to mitigate supplier risks
  • Conduct quality due diligence for business development initiatives
  • Build relationships to align quality expectations and resolve challenges

Benefits

  • Support for personal expression and open dialogue
  • Encouragement of professional growth
  • A workplace culture that values diversity and inclusion
  • Opportunities to impact healthcare positively
  • Emphasis on collaboration and strong partnerships
Full Job Description

The Position

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.

As a GXP Supplier Manager for Supplier Quality you will drive compliance excellence across our external supplier (Direct Materials and Service Providers) network and safeguard product quality throughout the supply chain. This versatile role offers the unique opportunity to combine hands-on supplier oversight with enterprise-wide quality leadership, including strategic initiatives like quality due diligence and early-stage program support. You will serve as a trusted expert in Suppliers’ regulatory compliance and operational excellence, directly impacting our mission to deliver safe, high-quality products to patients.

The Opportunity:

  • Oversee quality activities from supplier (Direct Materials and Service Providers) selection through decommissioning, including process validations, audits, Health Authority inspections, investigations, and regulatory submissions.
  • Create, negotiate, and sustain Quality Agreements with external suppliers and partners, rigorously monitoring compliance and addressing any deviations or gaps.
  • Manage critical quality functions for product release, such as batch review, investigation resolution, and change assessment, ensuring strict cGMP compliance.
  • Collaborate with external suppliers to keep manufacturing processes, specifications, and analytical methods in a validated, regulatory-compliant state.
  • Develop and maintain quality risk management plans to proactively identify and mitigate supplier compliance risks while driving continuous operational excellence.
  • Expand your impact through strategic initiatives, such as conducting quality due diligence for business development and representing Quality on early-stage Technical Development Teams.
  • Build strong relationships across internal and external partners to align quality expectations and quickly drive the interdepartmental resolution of complex regulatory challenges.

Who You Are:

  • You bring at least 10+ years of industry experience, with direct expertise in managing external suppliers and a deep understanding of supplier quality management and compliance.
  • You hold a Bachelor's degree in life sciences, pharmaceutical sciences, chemistry, or have equivalent professional experience demonstrating comparable knowledge in a related industry.
  • Demonstrated experience managing supplier and service provider relationships is highly valued.
  • You possess comprehensive knowledge of cGMP, ISO standards, and international pharmaceutical regulations, with a proven ability to interpret and apply these standards to supplier environments.
  • You are an excellent communicator (fluent in oral and written English) who can articulate complex quality concepts clearly to diverse audiences, from regulators to internal leadership.
  • You are proficient with standard office tools (Microsoft Office or Google Suite) and are available for occasional domestic or international travel (up to 10% annually) to conduct audits and oversee quality on-site.

**This role is not eligible for relocation**

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.

About Roche

Roche Holding AG is a Swiss multinational healthcare company that operates worldwide under two divisions: Pharmaceuticals and Diagnostics. Its holding company, Roche Holding AG, has bearer shares listed on the SIX Swiss Exchange. The company headquarters are located in Basel. Roche is the largest pharmaceutical company in the world, and the leading provider of cancer treatments globally. The company also produces a range of diagnostic tests for medical professionals and patients. Roche was one of the first companies to bring targeted treatments to patients. In 2019, Roche had over 100,000 employees worldwide, and generated revenue of CHF 61.5 billion.
Learn more about Roche
Size
100,920 employees
Industry
NASDAQ

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