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Manufacturing and Supply

Manufacturing and Supply
Where the
miracles of
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HSE Site Manager

Riells i Viabrea, Spain
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At a glance

Our teams produce and deliver over 4 billion units of medicines and vaccines every year, ensuring every breakthrough gets to the people who need it most.
Our state-of-the-art facilities, AI-powered smart factories, and cutting-edge automation are redefining what’s possible: ensuring treatments reach patients faster, safer, and more sustainably than ever before. This is where your skills, ambition, and passion can shape the future of healthcare.

BUSINESS AREA: Industrial Affairs

LOCATION: Riells i Viabrea

JOB PURPOSE

The HSE Manager is responsible for the Occupational Risk Prevention Service at the Riells plant and ensures that all necessary activities are carried out to comply with the Group’s Health, Safety, and Environment (HSE) policy and regulatory standards. This includes covering all areas of occupational risk prevention, either through internal resources or by engaging External Prevention Services, to guarantee the safety of people and assets and protect the environment at the Riells production site.

This position is part of the Site Management Committee and reports directly to the Site Head. The role also includes managing the HSE team of two professionals.

 About Job

JOB RESPONSABILITIES

· Ensure coverage of the three technical specialties: Workplace Safety, Industrial Hygiene, and Ergonomics & Psychosociology.

· Define and implement the HSE Management System (Health, Safety, and Environment) at the Riells Industrial Site to foster a preventive culture and continuous improvement, aiming to prevent accidents, occupational diseases, and minimize the environmental impact of site activities.

· Develop and implement a set of instructions and procedures to ensure compliance with applicable legislation and company policies and requirements in the HSE domain.

· Perform the duties of a Prevention Technician in accordance with Royal Decree 39/1997.

· Define and coordinate the implementation of the Riells Preventive Plan.

· Conduct and maintain updated risk assessments for all technical specialties at the Riells site.

· Investigate HSE incidents and accidents, including environmental ones.

· Define and monitor corrective and preventive action plans.

· Define PPE requirements for each job position and ensure their availability for all site employees.

· Establish communication channels to facilitate reporting of accidents, incidents, and risk situations by any worker at the Riells site (including company employees, temporary staff, or external collaborators).

· Defining and implementing procedures and instructions to ensure compliance with all legal and company HSE requirements.

· Define and ensure compliance with the training and information plan for all Riells employees to guarantee they have the necessary knowledge in occupational risk prevention.

· Act as the HSE contact person for the Safety and Health Committee and may be a member of this committee.

· Define and implement the Emergency Plan and procedures for action in case of occupational or environmental accidents.

· Act as the Emergency Manager and Crisis Management Coordinator.

· Develop and implement a management system to enhance sustainability and reduce the environmental impact of the Riells site.

· Coordinate the environmental impact assessment of the Riells site.

· Define an action plan with preventive and corrective measures to ensure compliance with applicable environmental legislation and mitigate the site's environmental impact as much as possible.

COORDINATOR OF SITE SECURITY

· Act as the site contact for coordinating corporate-defined security activities.

· Ensure implementation of security actions as instructed.

· Report any security incidents occurring at the site to corporate security services.

· Serve as the contact for the security service provider at Riells.

· Act as liaison with authorities for any security incidents, required information, or exceptional measures.

KPIs TO REPORT

1. Cycle Time and Lead Time: Cycle time measures the duration needed to complete a specific production process, while lead time tracks the total time from order to delivery

2. Capacity Utilization: Indicates how much of the production capacity is being used, helping to identify underutilization or overloading

3. Inventory Turnover Rate: Measures how often inventory is sold and replaced over a period, indicating the efficiency of inventory management

4. First Pass Yield (FPY) measures the percentage of products that meet quality standards without rework

5. Right First Time (RFT): tracks the percentage of processes completed correctly the first time

6. Downtime: Tracks the amount of time production is halted due to equipment failure, maintenance, or other issues

7. Compliance Rate: Measures adherence to regulatory requirements and internal quality standards, ensuring products meet safety and efficacy standards

8. Cost per Unit: Calculates the cost to produce one unit of product, helping to manage production costs and improve profitability

9. Scrap Rate: Measures the percentage of materials wasted during production, indicating efficiency and areas for improvement

10. On-Time In-Full (OTIF) Delivery Rate: Measures the percentage of orders delivered on time and in full, reflecting the reliability of the supply chain

11. Employee Training Hours: Tracks the number of hours employees spend in training, ensuring they are up to date with the latest practices and regulations

 About you

REQUIRED SKILLS

  • Leadership: Ability to lead and motivate a team to achieve production goals.

  • GMP Knowledge: Understanding of Good Manufacturing Practices (GMP) to maintain compliance with industry standards

  • Management: Overseeing staff schedules, maintaining morale, and developing training programs

  • Teamwork: Collaborating effectively with team members to work towards shared goals.

  • Communication: Both verbal and written communication skills are essential for interacting with staff, vendors, and senior management

  • Problem-Solving: Identifying and resolving issues that arise during the production process

  • Project Management: Planning, executing, and closing projects efficiently

  • Time Management: Prioritizing tasks to meet deadlines and ensure smooth operations

  • Attention to Detail: Ensuring precision in production processes to avoid errors

  • Adaptability: Ability to adapt to changes in regulations and production demands

  • Technical Skills: Knowledge of production processes and proficiency in relevant software

  • Safety Management: Ensuring a safe working environment and adherence to safety protocols

  • Quality Control: Ensuring products meet quality standards and implementing quality assurance protocols

  • Knowledge and experience related to the manufacturing and conditioning processes of pharmaceutical products.

REQUIRED TRAINING

PROFESSIONAL AND TECHNICAL SKILLS

·  Security at Issue HSE instructions and procedures applicable to the entire site

·  Establish HSE diagnostics and assessments

·  Develop risk management programs and evaluate their costs

·  Assess the safety level of installation or equipment

·  Analyze risks, make appropriate decisions, and alert Management if necessary

·  Study workstations and risk exposure measurements

·  Issue recommendations for workstation and workplace arrangements

·  Master's degree in HSE or equivalent training

HUMAN AND RELATIONAL SKILLS

·  Coordinate emergency response/interventions in case of accidents

·  Argue and convince internally on risk management and their consequences

·  Raise awareness and train on hygiene, safety, and environmental approach and risk prevention

·  Advise different departments on HSE matters

·  Manage the HSE team

PROFESSIONAL AND TECHNICAL

  • Official Training Master of Workplace Safety, Industrial Hygiene, and Ergonomics & Psychosociology (Real Decret 39/1997 “Reglamento de los Servicios de Prevención”)

  • English Advanced

  • Educational Background: Typically, a bachelor's degree in chemistry, chemical engineering, or a related field is required. Advanced degrees (e.g., master's or Ph.D.) can be advantageous.

  • GMP Training: Good Manufacturing Practices (GMP) training is essential. This includes understanding the regulations and guidelines that ensure products are consistently produced and controlled according to quality standards

  • Regulatory Knowledge: Familiarity with regulatory requirements from bodies like the FDA (21 CFR 211.25) and EMA is crucial. This includes training on compliance, quality control, and safety standards

  • Role-Specific Training: Training tailored to the specific tasks of a production manager, such as quality control, manufacturing processes, and supervisory skills, is important. This can include hands-on training, mentoring, and assessments

  • Environmental Postgraduate

  • Continuous Education: Ongoing training to stay updated with the latest industry trends, technologies, and regulatory changes is necessary. This can be achieved through workshops, seminars, and online courses


TAKE THE LEAD - BEHAVIOURS

Our ambition is fueled by a culture of high performance and belonging, underpinned by four core values: Aim Higher, Act for Patients, Be Bold, and Lead Together.:

Aim Higher: Focus on what matters, set high standards and move with urgency to deliver at speed. Learn from setbacks to achieve tomorrow’s breakthroughs.

Act for Patients: Improving patients’ lives drives everything we do, every day. We aim for simplicity and partner with others to go faster and further for patients. We eliminate barriers to access.

Be Bold: Take thoughtful risks, seize opportunities and think beyond what’s possible to accelerate our science and drive compelling growth.

Lead Together: Build trust and collaborate openly on our shared goals, celebrate collective wins 

and foster a sense of belonging.

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Pursue Progress. Discover Extraordinary.

Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.

Watch 'One day at Sanofi' and check out our Diversity Equity and Inclusion initiatives at sanofi.com

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Why work with us

  • We’re problem-solvers and pioneers. United by the belief that everyone deserves a healthier future. We create best-in-class vaccines that prevent disease and protect lives.

  • Innovation drives us. From AI and mRNA to next-gen science, we push the boundaries to deliver first- and best-in-class vaccines for infectious diseases worldwide.

  • Growth happens here. With bold investments in R&D and world-class facilities, Sanofians across the entire vaccine lifecycle are shaping the future of global health.

  • We do what’s right. Sustainability and DE&I drive our positive global impact—because the diverse communities Sanofians represent are the patients we serve.

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At Sanofi, diverse perspectives fuel the best solutions for patients. Hear from Monique Vessey, our Supply Chain Transformation Leader, on how her background shapes her approach to delivering life-changing medicines.

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