Freelancer profile translated to English.
Back to original languageAbout Bohemond
Independent consultant specializing in documentary quality and technical writing SOP/QMS for medtech and industry.
I help companies structure, create, or optimize their procedures, operating procedures, and quality documents so that they are clear, compliant with standards (ISO 13485, ISO 14971, EN 9100…), and easy to apply in the field.
My experience covers both regulated environments (MedTech, certification bodies) and the aeronautics industry (R&D and production).
- What I bring you
→ Compliant SOPs, ready to be signed and integrated into your quality system
→ Visual workflows, practical guides, and actionable checklists
→ Onboarding and training materials that accelerate the adoption of tools and processes (video format possible)
- Example of missions carried out
→ Medical device certification body - 20 months
Structuring of an ERP through a vade-mecum of best practices. Creation of SOPs compliant with ISO 13485 / ISO 14971. Development of workflows, training materials, and BPMN.
🧰 Services offered on Malt
💡 ISO / QMS Quality Documentary Audit
→ Analysis of 5 existing SOPs or quality documents + corrections + prioritized action plan.
💡 Custom SOP Creation Pack
→ 10 complete SOPs + BPMN workflows + practical guides + training sessions.
💡 À la carte SOP Writing
→ Individual SOP written according to your specifications.
💡 Process Onboarding & Training Kit
→ Onboarding manual + video training materials.
💡 ERP Documentary Optimization
→ Mapping of processes in your ERP + writing of user operating procedures.
- Deliverables provided in Word, PDF, PowerPoint, MP4
Languages: French & English
Intervention: 100% remote or hybrid, France & international
French
Native or bilingual
English
Native or bilingual
Remote only
Primarily works remotely
Experience
- Signal'EticCo-founder & CEOARCHITECTURE AND URBAN PLANNINGDecember 2024 - Today (1 year and 6 months)Toulouse, FranceImplementation of standardized procedures for the production, installation, and quality control of signs throughout France. Formalization of operating procedures for working with regulated/classified sites. Creation of user and installation guides for teams and partners. Management of technical documentation related to products and projects.
- SAFRAN SEATSManagement of R&D projects for composite materialsAVIATION AND AEROSPACEJune 2022 - August 2022 (2 months)Paris, FranceParticipation in R&D projects on innovative processes (composites, additive manufacturing) with the implementation and updating of associated technical documentation. Writing and structuring of test reports and process sheets, in collaboration with methods, quality, and production teams. Coordination with suppliers to integrate their processes into the internal documentation system.
- GMED SASTechnical Writer SOPMEDICALJune 2022 - March 2024 (1 year and 9 months)Washington, United States- Writing of multi-profile SOPs – clear procedures adapted to different user classes- Mapping / documentation of ERPs (CRM, HR, etc.) – step-by-step description of flows and best practices- Design of training & onboarding materials – preparation of sessions and guides to accelerate tool adoption- Mastery of ISO 13485 / medical device requirements – guarantee of FDA/EU regulatory compliance- Market research and analysis for an international project
Reviews
Recommendations
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Education
- European School of Materials Engineering (EEIGM)
Certifications
- Cambridge C1Cambridge2022
- DELE B2DELE2024