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Tech Transfer Officer

ALGER

Catégories: Ingénierie, Etudes, Projet, R&D
Secteur d'activité: Industries
Type de poste: CDI
Niveau d'études: Master 2, Ingéniorat, Bac + 5
Années d'experience: 3 À 5 Ans
Wilaya: ALGER
Publiée le: 26-03-2026 à 09:03:03

Description

The Technical Transfer Officer is responsible for leading and coordinating the transfer of pharmaceutical products from R&D to commercial manufacturing sites, ensuring full compliance with GMP requirements and regulatory standards.The role plays a strategic part in process optimization, cost efficiency, and external partner management (CMOs/CDMOs). The position requires strong cross-functional collaboration with R&D, Manufacturing, Quality, Regulatory Affairs, and Supply Chain to ensure successful product industrialization and lifecycle management.Job Requirements:Education: Bachelor’s, Master’s, or PhD degree in: Pharmaceutical Sciences, Chemistry, Biotechnology, Industrial Pharmacy, Or a related scientific fieldExperience: 2 or 3 years of experience in the pharmaceutical industry.Languages:Fluent in English (written and spoken).Technical Competencies:Bsic knowledge of cGMP regulations and pharmaceutical compliance requirements.Understanding of manufacturing processes (solid, liquid, sterile forms as applicable).Knowledge of documentation management and good documentation practices.Familiarity with quality systems (deviations, CAPA, change control).Personal Competencies:Good communication and stakeholder management abilities.Strong analytical and problem-solving skills.Ability to influence cross-functional and external teams.High level of organization and attention to detail.Resilience and ability to perform under pressure in complex environments.Change management capability and continuous improvement mindset. Duties and Responsibilities:Support the coordination and execution of technology transfer activities from R&D to manufacturing sites.Assist in the preparation, review, and archiving technical transfer documentation (protocols, reports, batch records, risk assessments).Ensure documentation compliance with GMP and internal quality standards.Coordinate communication between R&D, Production, Quality Assurance, Regulatory Affairs, and external partners (CMOs/CDMOs).Monitor transfer timelines and follow up on action plans to ensure project milestones are met.Support process validation activities (PPQ, cleaning validation, equipment qualification).Participate in risk assessments and gap analyses during transfer projects.Assist in change control, deviation management, and CAPA follow-up related to transfer activities.Contribute to data collection, analysis, and reporting during scale-up and industrialization phases.Support supplier visits, audits preparation, and technical meetings.

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