Bioreactor Production Technician

Jobtailor; Lyon; Sur place; EUR 52 000 - 78 000; Plein temps

Résumé du poste

Jobtailor in Lyon is seeking an experienced production professional to oversee pharmaceutical operations, ensure GMP compliance, and manage batch records and material flow. You will work with cross-functional teams to drive qualification, validation, and continuous improvement initiatives.

You bring 5–10 years in pharmaceutical production, strong communication, autonomous organization, and a solid grasp of GMP/traceability, with a proactive mindset to optimize performance while maintaining

Qualifications

• 5 to 10 years’ experience in a pharmaceutical production environment.
• GMP and traceability knowledge required.
• Experience with equipment qualification/validation is a plus.
• Autonomous, rigorous, organized, proactive and strong communicator.

Responsabilités

• Perform production operations in compliance with procedures and GMP.
• Complete batch records, computer systems, deviation forms and tracking documents.
• Contribute to the planning and organization of production activities.
• Manage raw materials, samples and inventory.
• Collaborate with support functions: Quality, Maintenance, Logistics, HSE, QC and Technical Support.
• Participate in the start-up and technical/organizational setup of production workshops.
• Plan, coordinate and take part in equipment and facility qualification activities.
• Carry out user-level maintenance and qualification tasks.
• Support commissioning and performance ramp-up of installations.
• Contribute to the writing and updating of operating documents.
• Help train future operators and new colleagues.
• Assist teams in becoming familiar with equipment and procedures.
• Take part in activity transfer projects and production implementation.
• Contribute to the deployment of solutions such as MES and raw material codification.
• Identify and implement technical and organizational improvements.
• Participate in continuous improvement and industrial performance initiatives.
• Ensure compliance with GMP and internal procedures.
• Adhere to and enforce HSE and biosafety requirements.
• Help maintain a compliant, safe and efficient production environment.

Connaissances

GMP Compliance

Equipment Qualification

Production Operations Management

Technical Degree in Industrial Prod

Stakeholder Collaboration

Formation

Technical degree (Bac+2 to Bac+5) in industrial production

Outils

MES Deployment

Production Workshop Setup

HSE Compliance

Biosafety Requirements

Description du poste

• Perform production operations in compliance with procedures and GMP
• Complete batch records, computer systems, deviation forms and tracking documents
• Contribute to the planning and organization of production activities
• Manage raw materials, samples and inventory
• Collaborate with support functions: Quality, Maintenance, Logistics, HSE, QC and Technical Support
• Participate in the start-up and technical/organizational setup of production workshops
• Plan, coordinate and take part in equipment and facility qualification activities
• Carry out user-level maintenance and qualification tasks
• Support commissioning and performance ramp-up of installations
• Contribute to the writing and updating of operating documents
• Help train future operators and new colleagues
• Assist teams in becoming familiar with equipment and procedures
• Take part in activity transfer projects and production implementation
• Contribute to the deployment of solutions such as MES and raw material codification
• Identify and implement technical and organizational improvements
• Participate in continuous improvement and industrial performance initiatives
• Ensure compliance with GMP and internal procedures
• Adhere to and enforce HSE and biosafety requirements
• Help maintain a compliant, safe and efficient production environment

Requirements

• Technical degree (Bac+2 to Bac+5) in industrial production, process engineering, biotechnology or equivalent
• 5 to 10 years’ experience in a pharmaceutical production environment
• Good knowledge of GMP and traceability requirements
• Experience in equipment qualification/validation is a plus
• Comfortable working with multiple stakeholders and on complex industrial projects
• Autonomous, rigorous, organized and proactive
• Strong communicator, able to unite teams around common objectives

Core Competencies

Demonstrates expertise in production operations within a pharmaceutical environment, ensuring compliance with GMP and internal procedures while effectively managing raw materials and inventory. Capable of leading equipment qualification activities and contributing to continuous improvement initiatives.

Highest-signal resume keywords

• GMP Compliance
• Equipment Qualification
• Production Operations Management
• Technical Degree in Industrial Production
• Stakeholder Collaboration

ATS Optimization Keywords

Hard Skills

• Batch Record Completion
• Deviation Form Management
• User-Level Maintenance
• Operating Document Writing
• Raw Material Management
• Production Activity Planning
• Performance Ramp-Up Support
• Technical Improvement Implementation
• Industrial Performance Initiatives
• Traceability Requirements Knowledge

Soft Skills

• Strong Communication
• Autonomous
• Organized
• Proactive
• Rigorous

Industry Keywords

• Pharmaceutical Production
• Process Engineering
• Biotechnology
• Continuous Improvement
• Quality Control

Tools & Technologies

• MES Deployment
• Production Workshop Setup
• HSE Compliance
• Biosafety Requirements