Full-Time

Quality Training Lead

Deadline 9/21/26
Sanofi

Sanofi

10,001+ employees

Global pharma company; vaccines and R&D

Compensation Overview

$78k - $112.7k/yr

Waltham, MA, USA

Hybrid

Hybrid work arrangement indicated.

Bachelor's

Category
Biology & Biotech (1)
Required Skills
GMP
Quality Assurance (QA)

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Requirements
  • A bachelor's degree or equivalent is required.
  • At least 5 years of experience is required in one or more of the following areas: training, learning management, quality, compliance, documentation, or quality assurance.
  • Educational experience will be considered.
  • Hands-on experience with Learning Management Systems is preferred.
  • Quality Assurance or compliance experience in pharmaceutical, biotechnology, or related industries is preferred.
  • Familiarity with GxP training requirements is preferred.
Responsibilities
  • Represent the Global Training Center at the senior level and act on behalf of Training Center leadership as needed to ensure continuity and strategic alignment across global operations.
  • Contribute to Communities of Practice by sharing expertise, elevating best practices, and driving innovation in training methodologies across the organization.
  • Own the end-to-end governance of training matrices, training plans, and learning content for the Global Training Center, ensuring alignment with GMP requirements, regulatory standards, and evolving business needs.
  • Establish and monitor key performance indicators to identify compliance gaps, assess training effectiveness, and lead targeted corrective actions.
  • Collaborate with VR&D departments across global sites to harmonize training practices and ensure consistency and regulatory alignment.
  • Partner with the Head of Global Training Center to design and execute strategic initiatives that simplify, standardize, and strengthen training programs at scale.
  • Serve as the training compliance subject matter expert for quality systems, including Deviations, CAPAs, and Change Controls, and provide guidance that protects product quality and patient safety.
  • Guide and support subject matter experts in creating and revising training materials and assessments, and review and approve content for compliance with training procedures and regulatory expectations.
  • Lead high-visibility pilot projects and global training initiatives.
  • Serve as the training subject matter expert to departments and functions, guiding them in developing compliant training materials, matrices, and iLearn curricula.
  • Act as the interface between the Learning Management System team and operational departments, and drive organizational compliance through actionable training plans.
  • Support audits and self-inspections by providing pre-audit documentation, responding to inspector requests, and demonstrating iLearn expertise.
  • Provide strategic guidance to improve training compliance across VR&D, identify systemic issues, and implement sustainable solutions.
  • Educate customers to navigate iLearn effectively and build compliance ownership.
  • Oversee and provide compliance guidance to the Global Training Center's decentralized administrators for VR&D, ensuring the iLearn platform maintains compliance and data integrity.
  • Liaise with the Global Learning Service team to resolve user and administrative issues in a timely manner.
  • Implement system improvements that enhance compliance tracking.

Sanofi is a global pharmaceutical and biotechnology company that develops, manufactures, and sells prescription medicines, over-the-counter products, and vaccines. Its products span immunology, oncology, rare diseases, and vaccines, addressing unmet medical needs through a strong focus on research and development. Sanofi's core product model relies on large-scale R&D, strategic partnerships, and licensing to bring new therapies to markets, with revenue generated from product sales and collaborations. The company differentiates itself by leveraging its global reach, diverse portfolio, and emphasis on patient-centric solutions, safety, and quality to navigate regulatory environments in developed and emerging markets. The company’s goal is to improve health outcomes and quality of life for people worldwide by delivering innovative treatments and vaccines that meet unmet medical needs.

Company Size

10,001+

Company Stage

IPO

Headquarters

Paris, France

Founded

1973

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Simplify Jobs

Simplify's Take

What believers are saying

  • Q2 2026 sales rose 17.8%; Dupixent topped €5.2 billion for the quarter.
  • July 30 upgraded 2026 guidance to around 10% sales growth, with higher EPS.
  • August 4 MenQuadfi infant approval widens vaccine reach; Nexviazyme's June phase 3 readout strengthens pipeline.

What critics are saying

  • Dupixent faces tougher H2 2026 comparisons, threatening growth after the €5.2 billion quarter.
  • Cenrifki carries liver injury risk; strict monitoring can slow adoption and invite liability.
  • Dupixent concentration and Regeneron's November 2024 lawsuit threaten Sanofi's core growth engine.

What makes Sanofi unique

  • Dupixent and partnered launch engine generate repeatable immunology cash flows across geographies.
  • Sanofi converted 2026 approvals for Sarclisa Escena, Wayrilz, and Cenrifki into launches.
  • Paulo Fontoura's September 1 R&D mandate centralizes translational science and regulatory execution.

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Benefits

Health Insurance

Professional Development Budget

Parental Leave

Company News

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Jul 10th, 2026
Sanofi's Sarclisa Escena approved in US as first anticancer drug delivered via on-body injector

The US Food and Drug Administration has approved Sanofi's subcutaneous Sarclisa Escena for treating multiple myeloma, making it the first anticancer treatment administered through an on-body injector. The therapy uses Enable Injections' CirCLIQ device, which delivers the drug automatically with a retractable 30g needle. The approval was supported by the IRAKLIA phase 3 study, which demonstrated that Sarclisa Escena delivered via the on-body injector provided similar efficacy and safety compared to intravenous infusion, with significantly shorter treatment time and fewer infusion-related reactions. The study showed a 71.1% objective response rate in patients with relapsed or refractory multiple myeloma. More than 70,000 patients worldwide have been treated with Sarclisa-based regimens. The on-body injector aims to reduce physical burden on healthcare providers whilst offering patients greater convenience during treatment.

Yahoo Finance
Jul 5th, 2026
Sanofi appoints Paulo Fontoura as R&D chief to accelerate pharma pipeline transformation

Sanofi has appointed Paulo Fontoura as Executive Vice President and Global Head of Research & Development Pharma, effective 1 September. Based in Paris, Fontoura will oversee the company's innovation engine, spanning research, translational medicine, clinical development, and regulatory affairs. He succeeds Dr Houman Ashrafian, who is leaving to pursue new opportunities. Fontoura brings over 25 years of experience across academic medicine, translational science, and pharmaceutical innovation. The appointment comes as Sanofi drives an R&D transformation whilst progressing its pipeline across multiple therapeutic areas. Separately, MacroGenics confirmed it will receive $24.5 million in regulatory milestone payments from Sanofi following FDA accelerated approval of TZIELD to delay decline in endogenous insulin production in children. Sanofi is a global biopharmaceutical company focusing on immunology, rare diseases, and oncology.