Empresa:

Tecnimede Group

Descrição da Função

Tecnimede Group is a 40 years Portuguese multinational company that wants to improve and preserve human life and health through the development, production and marketing of pharmaceutical products with a strong focus on quality and technological innovation. The group covers the entire life cycle of the medicinal products for human use with a strong investment in research and development.

Exporting to more than 100 countries worldwide, it is present in 6 countries (Portugal, Spain, Italy, Morocco, Colombia and Brazil) with a strong focus in expanding internationally and building strategic partnerships.

We are looking for a Tech Transfer Technician to join our R&D unit and play a key role in bridging development and commercial manufacturing. Reporting to the Head of Tech Transfer Lead, you will be responsible for supporting the scale-up and transfer of pharmaceutical products, from laboratory and pilot scale to industrial production, ensuring seamless, compliant, and efficient handover to manufacturing sites.

This is a hands-on position for a professional who thrives at the intersection of formulation science, process understanding, and GMP-regulated operations.

Key responsibilities

• Execute and document technology transfer activities for solid, semi-solid, and/or liquid dosage forms, from R&D to pilot and commercial scale.
• Support process validation, engineering batches, and scale-up trials in collaboration with Formulation, Analytical Development, QA, Regulatory affairs, and Manufacturing teams.
• Prepare, review, and update technical transfer documentation, including Master Batch Records, Transfer Protocols, Risk Assessments, and Final Reports, in line with GMP and ICH principles.
• Participate in risk assessments, process capability studies, and deviation investigations during transfer activities.
• Coordinate equipment and process parameter alignment between the R&D center and receiving manufacturing sites.
• Ensure full compliance with internal SOPs, GMP, and regulatory requirements throughout the transfer lifecycle.
• Contribute to continuous improvement initiatives related to tech transfer processes, templates, and tools.

Requirements

• Degree in Pharmaceutical Sciences, Chemical Engineering, Pharmaceutical Technology, Chemistry, or a related field.
• 2-5 years of experience in a pharmaceutical or GMP-regulated environment, preferably in Tech Transfer, Formulation Development, Manufacturing Science, or Production.
• Solid understanding of pharmaceutical manufacturing processes and unit operations (e.g., granulation, compression, coating, blending, filling).
• Familiarity with GMP, GxP, and ICH guidelines.
• Experience in preparing and reviewing technical documentation (MBRs, protocols, reports).
• Strong analytical thinking, attention to detail, and structured problem-solving.
• Effective communication skills and the ability to work in cross-functional teams.
• Fluency in English (written and spoken).

"In accordance with the provisions of the GDPR and other legislation in force on personal data protection, the contracting company guarantees that the processing of your personal data is lawful, fair, transparent and limited to the purposes for which your data was collected."

Observações

Lisboa (Portugal)