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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
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 ComplianceEquipment QualificationProduction Operations ManagementTechnical Degree in Industrial ProductionStakeholder Collaboration
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Batch Record CompletionDeviation Form ManagementUser-Level MaintenanceOperating Document WritingRaw Material ManagementProduction Activity PlanningPerformance Ramp-Up SupportTechnical Improvement ImplementationIndustrial Performance InitiativesTraceability Requirements Knowledge
Soft Skills
Strong CommunicationAutonomousOrganizedProactiveRigorous
Tools & Technologies
MES DeploymentProduction Workshop SetupHSE ComplianceBiosafety Requirements
Industry Keywords
Pharmaceutical ProductionProcess EngineeringBiotechnologyContinuous ImprovementQuality Control
About the role
Key responsibilities & impact- 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
What you’ll need- 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
Benefits
Comp & perks- Between 9 and 12 RTT days per year (reduction of working time days)
- Swile meal card: €10 / day with employer contribution
- 100% public transport coverage or mileage allowance
- Referral bonuses and profit-sharing schemes
- Health insurance and provident benefits
- Regular after-work events to help everyone get to know each other