Full-Time

Digital MES Product Configuration Lead

Posted on 5/9/2026

Deadline 5/24/26
Sanofi

Sanofi

10,001+ employees

Global pharma company; vaccines and R&D

Compensation Overview

$124.8k - $174.8k/yr

+ Target Bonus

Toronto, ON, Canada

Hybrid

Category
Process Engineering
Required Skills
Middleware
PowerShell
Power BI
Microsoft Azure
C#
AWS
Oracle
HTML/CSS
Requirements
  • 10+ years work experience in Manufacturing/Automation domain
  • Demonstrated experience in a multicultural/multilanguage environment and in a matricial organization
  • Broad knowledge of Manufacturing Processes in industrial plants
  • Significant MES experience: market standards knowledge (solutions, technologies, integration), process industry within life science/pharmaceutical industries
  • Core Product/Model concept
  • Expertise in MES solution Werum PAS-X or Siemens OPCEnter Pharma execution
  • Strong knowledge Manufacturing Execution System, including Master Batch Record and Review by Exception business processes and relevant MES solutions/modules/functionalities
  • Strong Knowledge of pharma industry regulatory context (GxP)
  • Strong communication, and interaction skills. Able to drive change management
  • Knowledge of Solution architecture, infrastructure & integration (AWS, Azure, Windows / Oracle architectures, Middlewares, Cyber Security rules, low code platform such Mendix, mobility technologies...)
  • Knowledge of Digital Development technologies (eg. C#, VBscript, HTML, CSS, Powershell, XML)
  • Knowledge of Reporting tools (eg. Power BI, Crystal reports...)
  • Automation layer (SCADA, DCS, PLCs, industrial protocols)
  • Agile mindset, Accountability, reliability
  • Ability to challenge, open minded and active listening
  • Ability to collaborate and build effective network inside and outside Sanofi
  • Ability to evaluate processes/solution to improve performance and drive continuous improvement
  • Proven vision, ability to anticipate evolutions due to internal and external factors
  • Bachelor’s degree required in Engineering related field, or master in Computer Science or related field (or equivalent experience)
  • English
  • Frequent mobility (North America & Europe)
Responsibilities
  • Understand the business requirements (including analytics ones) for the various processes in their domain, be able to challenge, to consolidate and to extrapolate them in order to build solutions expendable to multi-GBU use cases and plant configuration
  • Provide functional & technical leadership during the full lifecycle and ensure adoption and adequate uses of the solution.
  • Maximize customer satisfaction considering also to minimize build and maintenance costs, and risks associated with fulfillment of Business needs
  • Propose innovative Digital solution to address new business needs creating competitive advantage
  • Implement the appropriate services to ensure optimal allocation of all available capabilities
  • Ensure functional lead & expertise to project teams across the MARS program & the sites
  • Facilitate the transfer of know-how, experience and best practices
  • Contribute to Digital skills development within your domain
  • Design and build core solutions as close to standard market solutions as possible,on the basis of state-of-the-art best practices and aiming at aligning processes and enabling industrial efficiency across the different industrial sites of Sanofi.
  • Contribute of the on-time delivery of projects of domain ensuring robust, cost effective solutions while ensuring customer satisfaction, and business value focus
  • Safeguard the proper deployment of core solutions on the different industrial sites
  • Evaluate impact analysis on solution options and assesses and manages associated risks
  • End-to-end business process analysis including integration with partner systems (ERP, other shopfloor systems, automation layers), labelling technologies, and mobile technologies
  • Participate in the definition of indicators for performance and quality of service, monitor and communicate them
  • Ensure the compliance of the solutions within the area in relation to legal and regulatory requirements
  • Remain current on technology trends and Benchmark with other companies and partners to bring innovative inputs to our solutions, operating models and to our strategy
  • Collaborate with peers (Enterprise Architects, other solution architects, Cybersecurity team, technical architects…) to review solution design and/or introduction of new technology to ensure compliance with Sanofi standards
  • Explains / presents architecture and technical matters in an understanding way to Digital management team, staff and business stakeholders. Able to explain complex matters in a simple and understandable way
  • Breaks current Gxp Validation established postulates to simplify and adapt to current and next generation technologies & methodologies (Cloud, Service Management, Agile), without Quality regression on documentations and validation processes
Desired Qualifications
  • Successful and significant Project Management experience would be a plus
  • Any other items considered desirable or preferred in the posting should be listed here if present

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

Simplify Jobs

Simplify's Take

What believers are saying

  • Pharma launches sales surged 49.6% to €1.2B in Q1 2026 from Ayvakit and ALTUVIIIO.
  • Dupixent generated €4.2B in Q1 2026 across nine indications, driving 13.6% sales growth.
  • Analysts project 16.4% undervaluation with fair value €95.53 versus €79.82 share price.

What critics are saying

  • Dupixent patents expire 2031, enabling Mylan and Teva generics to erode €4.2B quarterly sales.
  • Regeneron reimbursements drop €400M in 2026, slashing amlitelimab phase 3 funding.
  • GSK Arexvy captures 60% RSV market share, halving Beyfortus €284M Q1 sales by 2027.

What makes Sanofi unique

  • Venglustat crosses blood-brain barrier as oral GCSi for GD3 neurological symptoms.
  • LEAP2MONO phase 3 trial superior to ERT on neurological endpoints at week 52.
  • FDA Breakthrough Therapy designation for venglustat in GD3 on March 18, 2026.

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Benefits

Health Insurance

Professional Development Budget

Parental Leave

Company News

Novo Holdings
May 4th, 2026
Novo Holdings joins $165 million crossover financing for Windward Bio to advance pipeline of long-acting immunology therapies with best-in-disease potential.

Novo Holdings joins $165 million crossover financing for Windward Bio to advance pipeline of long-acting immunology therapies with best-in-disease potential. * Led by OrbiMed, with participation from RA Capital Management, Janus Henderson Investors, Sanofi Ventures, and existing investors, including Novo Holdings * Proceeds will advance lead candidate WIN378 into Phase 3 and WIN027 into respiratory and dermatology studies by Q4 2026 * WIN378 has the potential to be the first-to-market ultra long-acting anti-TSLP antibody for asthma and COPD * WIN027 is a long-acting bispecific targeting TSLP and IL-13 with best-in-disease efficacy potential Windward Bio, a private, clinical-stage biotechnology company committed to improving outcomes for people living with serious immunological diseases, today announced an upsized $165 million crossover financing led by OrbiMed, with participation from existing Series A investors including Novo Holdings, Blue Owl Healthcare Opportunities, SR One, Omega Funds, RTW Investments, Qiming Venture Partners, Quan Capital, and Pivotal bioVenture Partners. The financing also included new investors RA Capital Management, Janus Henderson Investors, and Sanofi Ventures. Proceeds will significantly extend the company's cash runway and enable multiple clinical readouts in the next 12 months. Since launching in January 2025, Windward Bio has in-licensed 2 clinical-stage assets, raised $365 million, and rapidly advanced both programmes[RW1] in the clinic. WIN378, the lead programme, is a next-generation, fully human monoclonal antibody that potently binds to the thymic stromal lymphopoietin (TSLP) ligand. This well-validated cytokine plays a key role in the development and progression of a wide array of immunological diseases. WIN378 has the potential to be the first-to-market, ultra long-acting anti-TSLP antibody with twice-yearly dosing. The financing will accelerate the development of WIN378, which is currently being studied in the Phase 2/3 POLARIS programme in asthma. The Phase 2 dose-ranging component of POLARIS is fully recruited, with initial data expected in the second half of 2026. The first Phase 3 study of WIN378 is expected to begin in the fourth quarter of 2026. The Phase 2 SIRIUS study in chronic obstructive pulmonary disease (COPD) is anticipated to start in the second quarter of 2026. WIN027, the second programme, is a highly potent, long-acting bispecific antibody targeting both TSLP and interleukin-13 (IL-13) - two well-validated and synergistic drivers of inflammation in severe asthma, COPD, and atopic dermatitis. WIN027 is currently in a Phase 1 study with data readout expected by the end of 2026. The financing will support multiple proof-of-concept studies across respiratory and dermatology indications starting in in the fourth quarter of 2026. "We are excited to expand our shareholder base of top-tier investors to include RA Capital, Janus Henderson, and Sanofi Ventures" said Luca Santarelli, MD, Founder, Chief Executive Officer, and Board Chair of Windward Bio. "This financing further strengthens our balance sheet and allows us to further advance our programmes of next-generation therapies for patients living with serious respiratory and dermatological diseases." Naveed Siddiqi, Senior Partner, Venture Investments, Novo Holdings, said: "Spearheaded by a highly experienced clinical and commercial leadership consisting of serial entrepreneurs, Windward Bio has made rapid progress since it launched in 2025, including bringing in a second clinical stage asset, WIN027. There is much more to be done towards improving dosing frequency and outcomes for the benefit of patients suffering from serious and chronic immunological conditions, and as a significant shareholder, we are pleased to support Windward Bio as it advances its innovative and developing pipeline into late-stage trials." About WIN378 WIN378 is a next-generation, fully human monoclonal antibody that potently inhibits the TSLP ligand. This clinically validated target plays a key role in the development and progression of a wide array of immunological diseases, including asthma and COPD. WIN378 has been engineered to achieve half-life extension (HLE) and to have a silenced effector function. It has been studied in a Phase 1 trial, which confirmed an extended half-life suitable for twice-yearly dosing, demonstrated a low rate of antidrug antibodies, and was safe and well tolerated up to the highest dose tested. WIN378 is administered subcutaneously. Windward Bio licensed the global rights (excluding Greater China and several Southeast and West Asian countries) for WIN378 from Kelun Biotech (also known as SKB378) and Harbour BioMed (also known as HBM9378). WIN378 is currently being evaluated in the POLARIS Phase 2/3 asthma study with initial readouts expected in the second half of 2026. A Phase 2 study in COPD is anticipated to begin in the second quarter of 2026. About WIN027 WIN027 is a potential best-in-class, humanised bispecific monoclonal antibody with subpicomolar affinity for TSLP and IL-13, well-validated targets in immunological conditions. It has been engineered to achieve an extended half-life and enable less frequent dosing. Through this dual, long-acting inhibition, WIN027 is designed to set a new standard of efficacy in conditions such as asthma, COPD, and atopic dermatitis, potentially delivering deeper and more durable disease control than existing biologics. WIN027 is currently in Phase 1. Windward Bio licensed the global rights (excluding Greater China) for WIN027 from Qyuns Therapeutics (also known as QX027N). About Windward Bio Windward Bio is a clinical-stage biotechnology company with deep discovery, development, and commercialization expertise committed to transforming the treatment of people living with serious immunological conditions. Its lead programme is WIN378, a potential best-in-disease, ultra long-acting anti-TSLP monoclonal antibody currently in a Phase 2/3 trial for asthma. The pipeline also includes WIN027, a clinical-stage, long-acting anti-TSLPxIL-13 bispecific with broad therapeutic potential across immunological diseases, which is currently in Phase 1. The company is building a discovery pipeline of long-acting bispecific antibodies, targeting validated biology in respiratory and dermatological conditions. Media Enquiries Marie-Louise Jersin, Senior Communications Lead, [email protected]

Yahoo Finance
Apr 13th, 2026
Dupixent approved in EU as first targeted medicine for chronic spontaneous urticaria in children aged 2-11

Regeneron Pharmaceuticals and Sanofi announced that the European Commission has approved Dupixent (dupilumab) for treating moderate-to-severe chronic spontaneous urticaria in children aged 2 to 11 years. The approval applies to patients with inadequate response to histamine-1 antihistamines who are naïve to anti-immunoglobulin E therapy. This expands Dupixent's existing EU approval for CSU, which previously covered adults and adolescents aged 12 and older. The drug is now approved for children under 12 across four chronic diseases driven partly by type 2 inflammation. The approval is based on data from the LIBERTY-CUPID clinical trial programme, including efficacy data extrapolated from two Phase 3 adult trials and pharmacokinetic, safety and efficacy data from the CUPIDKids Phase 3 trial in children aged 2 to 11.

The Associated Press
Apr 13th, 2026
EU approves Sanofi and Regeneron's Dupixent as first targeted medicine for young children with chronic urticaria

The European Commission has approved Dupixent (dupilumab) for treating moderate-to-severe chronic spontaneous urticaria in children aged two to 11 years with inadequate response to antihistamines. Developed by Sanofi and Regeneron, this marks the first targeted medicine for young children with the condition in the EU. The approval, based on the LIBERTY-CUPID clinical study programme, expands Dupixent's CSU indication to children as young as two years. The drug is now approved for children under 12 across four chronic diseases driven partly by type 2 inflammation. Clinical studies showed Dupixent significantly reduced urticaria activity, including itch and hives, compared with placebo at Week 24. Safety results were consistent with Dupixent's known profile in dermatological indications. A supplemental biologics licence application is under review in the US for the same patient population.

The Associated Press
Mar 31st, 2026
Sanofi's Rezurock approved in EU for chronic graft-versus-host disease treatment

The European Commission has granted conditional marketing authorisation for Sanofi's Rezurock (belumosudil) to treat chronic graft-versus-host disease in adults and children aged 12 years and older weighing at least 40 kg. The treatment is approved for patients when other options provide limited benefit or have been exhausted. The approval follows a positive opinion from the European Medicines Agency and is based on the ROCKstar phase 2 study, which demonstrated a 74% overall response rate. Nearly half of chronic GVHD patients require third-line treatment, yet therapeutic options have remained limited in the EU. Rezurock is already approved in 20 countries, including the US, UK and Canada. More than 20,000 patients have been treated with the medicine since its first US approval in July 2021.

Yahoo Finance
Mar 30th, 2026
Bernstein initiates Sanofi with 'outperform' rating, $123 target price

Bernstein analyst Justin Smith has initiated coverage of Sanofi with an "Outperform" rating and a price target of €110, representing 37% upside from current levels. The analyst believes the French biopharmaceutical company's new chief executive will unlock shareholder value. Sanofi appointed Belén Garijo, former CEO of Germany's Merck KGaA, as its new chief executive in February. The 65-year-old Spanish executive will take charge in late April, replacing Paul Hudson after his six-year tenure. The company says Garijo will strengthen productivity, governance and innovation capacity in research and development. Sanofi shares have declined over 4.5% since the beginning of 2025. The stock trades at a forward price-to-earnings ratio of 9.26.