• Manager de Producción
• Ubicación: ES / Riells I Viabrea / Riells
  
  

Job Purpose

Coordination of all actions means and resources to be implemented at site level to ensure the optimization of industrial performance. As site leadership team member, participate on the definition of the strategic roadmap (vision, mission and objectives) in collaboration with all departments.

Job Responsabilities

• Performance monitoring of the production technical team, defining and proposing training actions and ensuring the necessary polyvalency to guarantee de production activity.
• Efficiency: Streamline production processes to maximize productivity and minimize waste.
• Management of the activity and resources foreseen in the budget of the production unit.
• Participate in the definition of the activity in the medium and long term together with the supply chain planner.
• Mid-term review of the production program with the production unit team (planner, AQP and engineer) to ensure the global coherence of the level of activity, maintenance, validations etc.
• Participation in the daily meetings of your APU: +QDCI, DCM, VSB etc.
• Definition and execution of the performance plan for the Production Unit. Coordinates the execution and monitoring together with the APU team.
• Coaching of technicians and operators in the field on the key issues regarding quality, safety and productivity.
• Ensure strict adherence to production planning and scheduling in units and added value, timely delivery of goods and support the plant's PCT
• Coordinates process performance and improvements with the PPM team, technicians, engineers and QA analysts.
• Resource Management: Ensure the availability of raw materials and equipment needed for production
• Monitoring: Track production progress and adjust schedules to address any delays or issues
• Inventory Management: Oversee inventory levels and order supplies as needed to avoid production disruptions
• Participate in the definition of the Quality Plan, as well as the action plans for the management of deviations to improve quality indicators.
• Define together with the APU and QA analysts the training actions and qualifications in the quality aspects of the personnel. Plan and ensure compliance with them.
• Analyze the product destructions of the Production Unit, defining action plans to avoid recurrence.
• Carry out field monitoring of key processes.
• Management of quality events and CAPAs for the Production Unit.
• Participation in investigations of critical deviations and claims.
• Ensure the correct state of documentation for the Production Unit, ensuring the compliance regarding auditees and regulatory authorities.
• Ensure, together with the APU technicians, compliance with the work instructions and procedures of your APU, respecting the good manufacturing practices and standards.
• Definition of the PASS and the HSE actions for the Production Unit.
• Lead and ensure respect for security. Accompany and promote the HSE culture with your APU team.
• Carry out observations and safety checks, as well as ensure that the Production Unit’s team carry out the observations and safety checks.
• Ensure, together with the technicians of your APU, the full implementation of actions plan derived from the investigations of security events.
• Quality Assurance: Ensure that the production process adheres to industry standards and safety regulations
• Problem-Solving: Identify potential delays or problems in the production process and devise solutions to overcome them
• Reporting: Prepare and present production reports to management, highlighting any issues and suggesting improvements
  
  

KPIs TO REPORT

• 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
• Capacity Utilization: Indicates how much of the production capacity is being used, helping to identify underutilization or overloading
• Inventory Turnover Rate: Measures how often inventory is sold and replaced over a period, indicating the efficiency of inventory management
• Materials consumption in the lines including detergents, ATEX products and consumables
• First Pass Yield (FPY) measures the percentage of products that meet quality standards without rework
• Right First Time (RFT): tracks the percentage of processes completed correctly the first time
• Downtime: Tracks the amount of time production is halted due to equipment failure, maintenance, or other issues
• Compliance Rate: Measures adherence to regulatory requirements and internal quality standards, ensuring products meet safety and efficacy standards. Deviations (significant or not)
• Cost per Unit: Calculates the cost to produce one unit of product, helping to manage production costs and improve profitability
• Scrap Rate: Measures the percentage of materials wasted during production, indicating efficiency and areas for improvement
• 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
• Employee Training Hours: Tracks the number of hours employees spend in training, ensuring they are up to date with the latest practices and regulations
  
  

Transversal Functions For People Managers

• Ensure that your work team complies with regulations (external or internal) regarding labor legislation, quality protocols, respect for the environment and safety at work.
• Promote the development of your team and actively participate in the talent management initiatives promoted in the company.
• Control compliance with team HSE procedures and instructions, especially, control the correct use of PPE and control the correct use of work equipment.
• Verify compliance with the HSE policy, the procedures and instructions of the HSE management system, requirements of workers, good condition of the work equipment, and possible external hiring/visits, etc.
• Report any change or incident regarding safety at work to the HSE team, or change, new requirement or quality incident to the quality team.
• Cost Control: Monitor production costs to ensure the process stays within budget, consumables, expenses, overtime, etc.
  
  

In The Scope Of Their Competences Within The Organization

• Verify compliance with the HSE requirements of external parties working in their area of responsibility.
  
  

Guarantee that your work team has the knowledge, training and information to carry out their work safely, and with the quality requirements that apply to the development of their duties.

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

• Educational Background: Typically, a bachelor's degree in pharmacy, 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
• 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
  
  

The person who occupies this position will be considered adequately trained, once he has been qualified following the instruction RIE-INS-001864 (see this qualification file and, failing that, the attached document).

PLAY TO WIN - BEHAVIOURS

Play To Win Is Our Corporate Strategy, a Concept That Aligns Our Way Of Working And Shows Us a Clearer Vision When It Comes To Achieving Objectives And Is Based On Four Behaviors

Do my best: I constantly look for ways to apply learning and drive improvement and try new things by taking calculated risks.

Take the initiative: I focus on what is important now, and on following up on what can be improved by prioritizing results over activity.

Acting in the interest of patients & clients: I always look out for what is best for our patients and clients in any solution I work on

Put Sanofi first: I look for what's best for Sanofi instead of what's best for me or my team and help everyone succeed.