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Bioproduction technician
Mastery of the fundamentals of biopharmaceutical manufacturing in a controlled environment, in accordance with the quality and regulatory requirements of the pharmaceutical industry.
CURRICULUM
Available in French, English
1 day of content
Goals
In summary
Prerequisites
This curriculum is intended for entry-level technical staff or individuals undergoing a career transition.
Participants should have:
Participants should have:
- a high school diploma to two-year post-secondary level (Bac to Bac+2) in science (biology, biochemistry, chemistry, biotechnology) or in industrial production
- or initial experience in a production environment (pharmaceutical, food industry, cosmetics)
- a basic understanding of hygiene, safety rules, and working in controlled areas
Course modules
1 day
Bioproduction technician
P7M7 Case Study applied to bioproduction facility operation (about 2 hours)
Important information : If you choose the accessible version of a 3D or virtual reality activity, please contact the support team to manually unlock the rest of the training.This module immerses the learner in the operational management of a bioproduction unit operating under cGMP conditions, integrating quality requirements, Health, Safety and Environment (HSE) constraints, and the practical handling of safety and quality deviations.It is grounded in Good Manufacturing Practices (GMP/cGMPs), HSE principles, problem-solving methodologies (such as the 5M diagram and the 5 Whys method), and covers the complete deviation management process—from identification and criticality assessment, to root cause investigation, and the implementation of Corrective and Preventive Actions (CAPA).Digital modalities : Activity 1: eLearning / Activity 2: Serious Game 3D / Activity 3: Serious Game 3DTarget audience : Employees integrating or working in R&D or bioproduction laboratories (senior technicians, engineers, researchers, managers) wishing to integrate the teams of Process Development and/or Technology Transfer.Personnel initiated in biotechnology working in support functions (Quality Assurance, Analysis, Regulatory), Partners (suppliers, subcontractors, consultants, CMOs) operating in bioproduction and pharmaceutical industry or Public from the academic environment wishing to understand the industrial environment and development issues, the technology transfer and biomedecine production.Evaluation procedures :A short evaluation at the end of the module confirming what you have learnt and enabling you to move to the next one ( 80% of correct answers required).
Data Quality and Integrity in Bioproduction: Principles and practical cases (about 2 hours)
This module presents the key principles of data integrity and their applications in bioproduction through concrete, real-life scenarios.It is based on the ALCOA++ principles, as well as the guidelines from the EMA and the FDA (21 CFR Part 11).Digital modalities : Activity 1: eLearning / Activity 2 : Serious Game 2D / Activity 3 : Serious Game 2DTarget audience :Newcomers (technicians, engineers, researchers, and managers) preparing to take up a position in bioproduction or wishing to update their knowledgeStudents and teachers seeking to discover the pharmaceutical industrial environment and the challenges associated with biopharmaceutical production.Support functions (maintenance, regulatory, Quality, HSE, supply chain, Lean, PMO, data) wishing to better understand the fundamentals of bioproduction professionsEmployees in commercial functions, market access, management or partners (suppliers, subcontractors, consultants, investors) not familiar with bioproduction but wishing to better understand the ecosystem and challenges of bioproductionEvaluation procedure :A short evaluation at the end of the module confirming what you have learnt and enabling you to move to the next one (no limit of attempts, 80% of correct answers required).Trainees enrolled in the whole curriculum have the possibility to assess and set their new knowledges and skills via an anchoring quiz between modules
P1M1 Discovering biopharmaceuticals: key development stages, regulatory framework, and manufacturing processes (about 1 hour)
Description : This module provides an introduction to biopharmaceuticals, their specific characteristics, the main stages of their development, and the production processes used in bioproduction.It is based on the regulatory frameworks governing the development of biopharmaceuticals, such as Good Manufacturing Practices (GMP), ICH guidelines, the requirements of regulatory agencies (EMA, FDA), as well as the key stages of production processes (USP, DSP, Fill & Finish).Digital modalities : Activity 1: eLearning / Activity 2 : eLearningTarget audience :Newcomers (technicians, engineers, researchers, and managers) preparing to take up a position in bioproduction or wishing to update their knowledgeStudents and teachers seeking to discover the pharmaceutical industrial environment and the challenges associated with biopharmaceutical production.Support functions (maintenance, regulatory, Quality, HSE, supply chain, Lean, PMO, data) wishing to better understand the fundamentals of bioproduction professionsEmployees in commercial functions, market access, management or partners (suppliers, subcontractors, consultants, investors) not familiar with bioproduction but wishing to better understand the ecosystem and challenges of bioproductionEvaluation procedure :A short evaluation at the end of the module confirming what you have learnt and enabling you to move to the next one (no limit of attempts, 80% of correct answers required).Trainees enrolled in the whole curriculum have the possibility to assess and set their new knowledges and skills via an anchoring quiz between modules
P1M2 Immersion in a cleanroom: preventing contamination and adopting best practices (about 2 hours)
Important information : If you choose the accessible version of a 3D or virtual reality activity, please contact the support team to manually unlock the rest of the training.This module covers the characteristics of cleanrooms, the associated contamination risks, and the expected gowning and behavioral practices in production environments.It is based on Good Manufacturing Practices (GMP), ISO standards, principles for controlling the production environment (air classes, airflow, biosafety levels, gowning), as well as on control equipment (laminar flow systems, filters...).Digital modalities : Activity 1: eLearning / Activity 2 : eLearning / Activity 3 : eLearning / Activity 4 : Virtual RealityTarget audience :Newcomers (technicians, engineers, researchers, and managers) preparing to take up a position in bioproduction or wishing to update their knowledgeStudents and teachers seeking to discover the pharmaceutical industrial environment and the challenges associated with biopharmaceutical production.Support functions (maintenance, regulatory, Quality, HSE, supply chain, Lean, PMO, data) wishing to better understand the fundamentals of bioproduction professionsEmployees in commercial functions, market access, management or partners (suppliers, subcontractors, consultants, investors) not familiar with bioproduction but wishing to better understand the ecosystem and challenges of bioproductionEvaluation procedure :A short evaluation at the end of the module confirming what you have learnt and enabling you to move to the next one (no limit of attempts, 80% of correct answers required).Trainees enrolled in the whole curriculum have the possibility to assess and set their new knowledges and skills via an anchoring quiz between modules
P5M1 Overview of Quality Control (about 2 hours)
This module covers the fundamentals of quality control (QC) in bioproduction, explaining its essential role in biopharmaceutical manufacturing, the types of tests performed, the documents and methods used, as well as sample and deviation management practices.It is based on Good Manufacturing Practices (GMP), quality documentation management standards, and equipment qualification guidelines. The module incorporates tools and methods such as sampling plans, validated control methods, In-Process Control (IPC) monitoring, sample traceability systems, and quality deviation analysis methods.Digital modalities : Activity 1: eLearning / Activity 2 : eLearning / Activity 3 : eLearningTarget audience :Newcomers (technicians, engineers, researchers, and managers) preparing to take up a position in bioproduction or wishing to update their knowledgeStudents and teachers seeking to discover the pharmaceutical industrial environment and the challenges associated with biopharmaceutical production.Support functions (maintenance, regulatory, Quality, HSE, supply chain, Lean, PMO, data) wishing to better understand the fundamentals of bioproduction professionsEmployees in commercial functions, market access, management or partners (suppliers, subcontractors, consultants, investors) not familiar with bioproduction but wishing to better understand the ecosystem and challenges of bioproductionEvaluation procedure :A short evaluation at the end of the module confirming what you have learnt and enabling you to move to the next one (no limit of attempts, 80% of correct answers required).Trainees enrolled in the whole curriculum have the possibility to assess and set their new knowledges and skills via an anchoring quiz between modules
P7M7 Case Study applied to bioproduction facility operation (about 2 hours)
Important information : If you choose the accessible version of a 3D or virtual reality activity, please contact the support team to manually unlock the rest of the training.This module immerses the learner in the operational management of a bioproduction unit operating under cGMP conditions, integrating quality requirements, Health, Safety and Environment (HSE) constraints, and the practical handling of safety and quality deviations.It is grounded in Good Manufacturing Practices (GMP/cGMPs), HSE principles, problem-solving methodologies (such as the 5M diagram and the 5 Whys method), and covers the complete deviation management process—from identification and criticality assessment, to root cause investigation, and the implementation of Corrective and Preventive Actions (CAPA).Digital modalities : Activity 1: eLearning / Activity 2: Serious Game 3D / Activity 3: Serious Game 3DTarget audience : Employees integrating or working in R&D or bioproduction laboratories (senior technicians, engineers, researchers, managers) wishing to integrate the teams of Process Development and/or Technology Transfer.Personnel initiated in biotechnology working in support functions (Quality Assurance, Analysis, Regulatory), Partners (suppliers, subcontractors, consultants, CMOs) operating in bioproduction and pharmaceutical industry or Public from the academic environment wishing to understand the industrial environment and development issues, the technology transfer and biomedecine production.Evaluation procedures :A short evaluation at the end of the module confirming what you have learnt and enabling you to move to the next one ( 80% of correct answers required).
Data Quality and Integrity in Bioproduction: Principles and practical cases (about 2 hours)
This module presents the key principles of data integrity and their applications in bioproduction through concrete, real-life scenarios.It is based on the ALCOA++ principles, as well as the guidelines from the EMA and the FDA (21 CFR Part 11).Digital modalities : Activity 1: eLearning / Activity 2 : Serious Game 2D / Activity 3 : Serious Game 2DTarget audience :Newcomers (technicians, engineers, researchers, and managers) preparing to take up a position in bioproduction or wishing to update their knowledgeStudents and teachers seeking to discover the pharmaceutical industrial environment and the challenges associated with biopharmaceutical production.Support functions (maintenance, regulatory, Quality, HSE, supply chain, Lean, PMO, data) wishing to better understand the fundamentals of bioproduction professionsEmployees in commercial functions, market access, management or partners (suppliers, subcontractors, consultants, investors) not familiar with bioproduction but wishing to better understand the ecosystem and challenges of bioproductionEvaluation procedure :A short evaluation at the end of the module confirming what you have learnt and enabling you to move to the next one (no limit of attempts, 80% of correct answers required).Trainees enrolled in the whole curriculum have the possibility to assess and set their new knowledges and skills via an anchoring quiz between modules
P1M1 Discovering biopharmaceuticals: key development stages, regulatory framework, and manufacturing processes (about 1 hour)
Description : This module provides an introduction to biopharmaceuticals, their specific characteristics, the main stages of their development, and the production processes used in bioproduction.It is based on the regulatory frameworks governing the development of biopharmaceuticals, such as Good Manufacturing Practices (GMP), ICH guidelines, the requirements of regulatory agencies (EMA, FDA), as well as the key stages of production processes (USP, DSP, Fill & Finish).Digital modalities : Activity 1: eLearning / Activity 2 : eLearningTarget audience :Newcomers (technicians, engineers, researchers, and managers) preparing to take up a position in bioproduction or wishing to update their knowledgeStudents and teachers seeking to discover the pharmaceutical industrial environment and the challenges associated with biopharmaceutical production.Support functions (maintenance, regulatory, Quality, HSE, supply chain, Lean, PMO, data) wishing to better understand the fundamentals of bioproduction professionsEmployees in commercial functions, market access, management or partners (suppliers, subcontractors, consultants, investors) not familiar with bioproduction but wishing to better understand the ecosystem and challenges of bioproductionEvaluation procedure :A short evaluation at the end of the module confirming what you have learnt and enabling you to move to the next one (no limit of attempts, 80% of correct answers required).Trainees enrolled in the whole curriculum have the possibility to assess and set their new knowledges and skills via an anchoring quiz between modules
P1M2 Immersion in a cleanroom: preventing contamination and adopting best practices (about 2 hours)
Important information : If you choose the accessible version of a 3D or virtual reality activity, please contact the support team to manually unlock the rest of the training.This module covers the characteristics of cleanrooms, the associated contamination risks, and the expected gowning and behavioral practices in production environments.It is based on Good Manufacturing Practices (GMP), ISO standards, principles for controlling the production environment (air classes, airflow, biosafety levels, gowning), as well as on control equipment (laminar flow systems, filters...).Digital modalities : Activity 1: eLearning / Activity 2 : eLearning / Activity 3 : eLearning / Activity 4 : Virtual RealityTarget audience :Newcomers (technicians, engineers, researchers, and managers) preparing to take up a position in bioproduction or wishing to update their knowledgeStudents and teachers seeking to discover the pharmaceutical industrial environment and the challenges associated with biopharmaceutical production.Support functions (maintenance, regulatory, Quality, HSE, supply chain, Lean, PMO, data) wishing to better understand the fundamentals of bioproduction professionsEmployees in commercial functions, market access, management or partners (suppliers, subcontractors, consultants, investors) not familiar with bioproduction but wishing to better understand the ecosystem and challenges of bioproductionEvaluation procedure :A short evaluation at the end of the module confirming what you have learnt and enabling you to move to the next one (no limit of attempts, 80% of correct answers required).Trainees enrolled in the whole curriculum have the possibility to assess and set their new knowledges and skills via an anchoring quiz between modules
P5M1 Overview of Quality Control (about 2 hours)
This module covers the fundamentals of quality control (QC) in bioproduction, explaining its essential role in biopharmaceutical manufacturing, the types of tests performed, the documents and methods used, as well as sample and deviation management practices.It is based on Good Manufacturing Practices (GMP), quality documentation management standards, and equipment qualification guidelines. The module incorporates tools and methods such as sampling plans, validated control methods, In-Process Control (IPC) monitoring, sample traceability systems, and quality deviation analysis methods.Digital modalities : Activity 1: eLearning / Activity 2 : eLearning / Activity 3 : eLearningTarget audience :Newcomers (technicians, engineers, researchers, and managers) preparing to take up a position in bioproduction or wishing to update their knowledgeStudents and teachers seeking to discover the pharmaceutical industrial environment and the challenges associated with biopharmaceutical production.Support functions (maintenance, regulatory, Quality, HSE, supply chain, Lean, PMO, data) wishing to better understand the fundamentals of bioproduction professionsEmployees in commercial functions, market access, management or partners (suppliers, subcontractors, consultants, investors) not familiar with bioproduction but wishing to better understand the ecosystem and challenges of bioproductionEvaluation procedure :A short evaluation at the end of the module confirming what you have learnt and enabling you to move to the next one (no limit of attempts, 80% of correct answers required).Trainees enrolled in the whole curriculum have the possibility to assess and set their new knowledges and skills via an anchoring quiz between modules
P4M4 Viral clearance (about 2 hours)
Information importante : Si vous choisissez la version accessible d'une activité 3D ou en réalité virtuelle, veuillez contacter le service d’assistance pour débloquer manuellement la suite de la formation.This module presents the sources of viral contamination, the viral clearance steps integrated into the DSP (purification) process, and the principles of viral validation studies.It details the mechanisms of virus inactivation and removal, the three pillars of viral safety, as well as the regulatory requirements governing validation studies.The content is based on ICH Q5A guidelines, cGMP practices, raw material risk assessment, and the methodology of conducting viral validation studies. Modalités digitales : Activité 1: Serious Game 2D / Activité 2: Serious Game 3D / Activité 3: Serious Game 2DTarget audience : Operators, technicians, production managers, continuous improvement and performance managers, engineering managers, maintenance staff, or project managers in the pharmaceutical, chemical, or biotechnology sectors.Collaborators joining or working at the interface of a bioproduction unit.Quality Assurance or Quality Control personnel operating in bioproduction.Students in life sciences, pharmacy, or chemistry, or individuals from academic backgrounds seeking to understand the industrial environment of biomedicine purification.Evaluation procedures : Une courte évaluation à la fin du module pour confirmer ce que vous avez appris et accéder au module suivant (80% de bonnes réponses requises).
P4M5 Equipment Cleaning in DSP (about 2 hours)
Important information : If you choose the accessible version of a 3D or virtual reality activity, please contact the support team to manually unlock the rest of the training.This module presents cleaning methods for equipment used in Downstream Processing (DSP), highlighting their essential role in preventing contamination and ensuring compliance with quality standards in bioproduction.It is based on cGMP guidelines, in-place cleaning (CIP) and sanitization (SaIP) techniques, validation strategies (3 consecutive batches), analytical criteria (endotoxins, pH, conductivity), as well as quality documentation (batch records, sampling procedures) and deviation investigation practices.Digital modalities : Activity 1: Serious Game 2D / Activity 2 : Serious Game 2D / Activity 3 : Serious Game 3DTarget audience : Operators, technicians, production managers, continuous improvement and performance managers, engineering managers, maintenance staff, or project managers in the pharmaceutical, chemical, or biotechnology sectorsCollaborators joining or working at the interface of a bioproduction unit.Quality Assurance or Quality Control personnel operating in bioproduction.Students in life sciences, pharmacy, or chemistry, or individuals from academic backgrounds seeking to understand the industrial environment of biomedicine purification.Evaluation procedures : A short evaluation at the end of the module confirming what you have learnt and enabling you to move to the next one ( 80% of correct answers required).
P4M6 In-Process Controls (IPCs) for DSP in cGMPs (about 2 hours)
This module presents In-Process Controls (IPCs) applied to the purification steps (Downstream Process – DSP) in a cGMP environment, highlighting their role in monitoring critical process parameters, managing contamination risks, and ensuring product quality.It draws on cGMP and ICH guidelines, analytical methods used for IPCs (pH measurement, conductivity, CE-SDS, cIEF, HPLC-SEC, qPCR, ELISA, LAL), sampling practices both in-zone and off-zone, the PAT initiative for in-line monitoring, as well as the concept of Critical Quality Attributes (CQAs) to ensure product quality throughout the processDigital modalities : Activity 1: eLearning / Activity 2 : Serious Game 2D / Activity 3 : Serious Game 2DTarget audience : Operators, technicians, production managers, continuous improvement and performance managers, engineering managers, maintenance staff, or project managers in the pharmaceutical, chemical, or biotechnology sectorsCollaborators joining or working at the interface of a bioproduction unit.Quality Assurance or Quality Control personnel operating in bioproduction.Students in life sciences, pharmacy, or chemistry, or individuals from academic backgrounds seeking to understand the industrial environment of biomedicine purification.Evaluation procedures : A short evaluation at the end of the module confirming what you have learnt and enabling you to move to the next one ( 80% of correct answers required).
P4M8 DSP - Applicative module (40 minutes)
Important information : If you choose the accessible version of a 3D or virtual reality activity, please contact the support team to manually unlock the rest of the training.This immersive module allows learners to practice advanced purification (DSP) steps in a cGMP environment, including affinity chromatography, tangential flow filtration (TFF), final 0.22μm filtration, and clean-in-place (CIP) procedures.It is based on cGMP guidelines, standard operating procedures (SOPs), in-process controls (IPCs), quality control (QC) sampling protocols, and real-world calibration and equipment verification practices.Digital modalities : Activity 1 : Virtual RealityTarget audience : Operators, technicians, production managers, continuous improvement and performance managers, engineering managers, maintenance staff, or project managers in the pharmaceutical, chemical, or biotechnology sectors.Collaborators joining or working at the interface of a bioproduction unit.Quality Assurance or Quality Control personnel operating in bioproduction.Students in life sciences, pharmacy, or chemistry, or individuals from academic backgrounds seeking to understand the industrial environment of biomedicine purification.Evaluation procedures : A short evaluation at the end of the module confirming what you have learnt and enabling you to move to the next one ( 80% of correct answers required).
P2M2 Presentation of cGMP and USP industrial environment (about 2 hours)
This module presents the fundamental principles of Good Manufacturing Practices (cGMP) as applied to cell culture (USP) in a controlled environment, detailing the various stages of the USP process and the requirements associated with each step.It is based on cGMP (Current Good Manufacturing Practices) guidelines, best practices in hygiene and equipment preparation, bioreactor-based cell culture techniques (real-time monitoring of critical parameters), harvesting procedures, as well as documentation, traceability, and cross-contamination risk control requirements throughout the process.Digital modalities : Activity 1 : eLearning / Activity 2 : eLearning / Activity 3 : eLearning 360° Target audience : Operators, technicians, production managers, continuous improvement and performance managers, engineering managers, maintenance staff, or project managers in the pharmaceutical, chemical, or biotechnology sectors.Collaborators joining or working at the interface of a bioproduction unit. Quality Assurance or Quality Control personnel operating in bioproduction.Students in life sciences, pharmacy, or chemistry, or individuals from academic backgrounds seeking to understand the industrial environment of cell culture.Evaluation procedures : A short evaluation at the end of the module confirming what you have learnt and enabling you to move to the next one ( 80% of correct answers required).
P2M4 In-Process Controls (IPCs) for USP in cGMP (about 2 hours)
This module presents the different types of controls performed during production in a USP environment to ensure the quality, integrity, and compliance of biological products, in accordance with cGMP requirements.It covers the categorization of In Process Controls (IPCs) – in-line, at-line, and off-line – the sampling protocols described in the sampling plan, documentation requirements (batch record), as well as deviation management and the implementation of corrective actions to support continuous process improvement.Digital modalities : Activity 1 : eLearning / Activity 2 : Serious Game 2D / Activity 3 : Serious Game 2DTarget audience : Operators, technicians, production managers, continuous improvement and performance managers, engineering managers, maintenance staff, or project managers in the pharmaceutical, chemical, or biotechnology sectors.Collaborators joining or working at the interface of a bioproduction unit. Quality Assurance or Quality Control personnel operating in bioproduction.Students in life sciences, pharmacy, or chemistry, or individuals from academic backgrounds seeking to understand the industrial environment of cell culture.Evaluation procedures : A short evaluation at the end of the module confirming what you have learnt and enabling you to move to the next one ( 80% of correct answers required).
P2M6 Practice USP in cGMPs (about 1 hour)
Important information : If you choose the accessible version of a 3D or virtual reality activity, please contact the support team to manually unlock the rest of the training.This module offers immersive simulations of typical operations in a USP process within a cGMP environment, while developing the reflexes needed to manage anomalies under real-life conditions.It is based on the application of cGMP best practices, deviation and root cause analysis, the implementation of corrective and preventive actions (CAPA), the use of production documentation for decision-making, as well as teamwork to assess risks and anticipate the impact of deviations on product quality.Digital modalities : Activity 1 : Virtual RealityTarget audience : Operators, technicians, production managers, continuous improvement and performance managers, engineering managers, maintenance staff, or project managers in the pharmaceutical, chemical, or biotechnology sectors.Collaborators joining or working at the interface of a bioproduction unit. Quality Assurance or Quality Control personnel operating in bioproduction.Students in life sciences, pharmacy, or chemistry, or individuals from academic backgrounds seeking to understand the industrial environment of cell culture.Evaluation procedures : A short evaluation at the end of the module confirming what you have learnt and enabling you to move to the next one ( 80% of correct answers required).
P10M1 Transportation and logistics management for bioproducts (about 2 hours)
Important information: If you choose the accessible version of the 3D activity, please contact the support team to manually unlock the rest of the training.This module explores the logistical challenges related to the transport of bioproducts throughout their life cycle, from production to patient delivery. It covers the specificities of logistics flows (domestic and international), transport modes, regulatory constraints, associated risks, and the responsibilities of the various stakeholders in the supply chain. A practical case study is also included to simulate the secure organization of a shipment. It is based on Good Distribution Practices (GDP), key international transport regulations (CMR – Convention on the Contract for the International Carriage of Goods by Road, Brussels Convention, Montreal Protocol, CIM – International Convention concerning the Carriage of Goods by Rail), INCOTERMS (International Commercial Terms), risk management tools (risk matrix, business continuity plan), as well as best practices for shipment security and customs compliance. Digital modalities: Activity 1 : eLearning / Activity 2 : eLearning / Activity 3 : eLearning / Activity 4 : Serious Game 3DTarget audience: Employees integrating or working in production sites, distribution centers, or in the transport and storage of pharmaceutical products and bioproducts (logistics, customs operations, export managers, customer service, supply chain, freight forwarders) wishing to acquire the fundamentals of logistics applied to bioproducts. Support functions (Quality Assurance, Quality Control, HSE) or partners (suppliers, subcontractors, consultants, CMOs) wishing to better understand the challenges of logistics applied to bioproducts. Evaluation procedure:A short evaluation at the end of the module confirming what you have learnt and enabling you to move to the next one ( 80% of correct answers required).
P3M2 Introduction to Fill & Finish (about 1 hour)
This module presents the key stages of the Fill & Finish process, including storage, formulation, filling, visual inspection, labeling, and packaging. It also introduces patient risks and their management, and details dosage forms as well as the stability of biopharmaceutical products.The module addresses patient risk management and the constraints related to the stability of biopharmaceuticals. It adopts a descriptive approach to the different product types (proteins, mRNA, cells), highlighting the differences with chemically derived pharmaceutical products, as well as the factors influencing their stability during formulation operations.Digital modalities : Activity 1: eLearning / Activity 2: eLearning Target audience : Newcomers (operators, technicians, engineers, researchers, and managers) preparing to take up a position in Fill & Finish (formulation, aseptic filling, and packaging roles) or wishing to refresh their knowledge.Students in life sciences, pharmacy, or chemistry, or individuals from academic backgrounds seeking to understand the industrial environment of Fill & Finish.Support functions (maintenance, regulatory affairs, Quality Assurance, Quality Control, HSE, etc.) wishing to better understand the fundamentals of Fill & Finish roles.Evaluation procedures :A short evaluation at the end of the module confirming what you have learnt and enabling you to move to the next one ( 80% of correct answers required).
Available in French, English
1 day of content
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