Job Description

Job Purpose:

The purpose of this position is to facilitate the seamless transfer of pharmaceutical processes and technologies from R&D to manufacturing or between manufacturing sites. This role ensures that processes are robust, scalable, and comply with regulatory standards, enabling successful product launches and commercial production.

Duties & Responsibilities:

• Lead the transfer of manufacturing processes from R&D to production or between manufacturing sites.
• Develop and manage project plans, timelines, and milestones for technology transfer projects.
• Coordinate cross-functional teams, including R&D, Quality, Regulatory, and Manufacturing, to ensure successful transfer activities.
• Manage scale-up from R&D/pilot to commercial scale, including process characterization and definition of proven acceptable ranges / design space.
• Τransfer the control strategy, including Critical Quality Attributes (CQAs) and Critical Process Parameters (CPPs), in line with QbD principles (ICH Q8–Q11).
• Coordinate raw material/excipient equivalence, equipment fit-gap assessment between sites, and analytical method transfer with QC.
• Prepare, review, and approve technology transfer documentation, including protocols, reports, batch records, and SOPs.
• Ensure compliance with regulatory requirements (FDA, EMA, etc.) and industry standards (ICH guidelines) throughout the transfer process.
• Maintain accurate and detailed records of all transfer activities and outcomes.
• Collaborate with manufacturing teams to troubleshoot and resolve process-related issues.
• Conduct risk assessments and develop mitigation strategies for potential process deviations.(applying FMEA / ICH Q9 risk-management methodology, including assessment of process gaps between sending and receiving sites).
• Provide technical training and support to manufacturing personnel on new processes and technologies.
• Act as a subject matter expert (SME) for transferred processes and provide ongoing technical support.
• Facilitate knowledge transfer and ensure the sustainability of new processes in the production environment.
• Communicate effectively with internal and external stakeholders to ensure alignment and transparency.
• Participate in cross-functional meetings and present updates on technology transfer progress.
• Foster a collaborative environment to drive continuous improvement and innovation.
• Support and/or lead process validation (PPQ) at the receiving site, and ensure equipment and facility qualification (IQ/OQ/PQ) status supports the transfer.
• Demonstrate product/process equivalence between sending and receiving sites (analytical comparability; side-by-side or bracketing batches).

Qualifications and Skills:

• Bachelor’s or Master’s degree in Chemical or Mechanical Engineering, Pharmaceutical Sciences, Biotechnology, or a related field.
• Master’s degree in a relevant field will be considered an advantage.
• At least 2 years of experience in pharmaceutical manufacturing, process development, or technology transfer.
• Effective interpersonal skills with the ability to work collaboratively across cross-functional teams.
• Strong verbal and written communication skills; ability to present technical information clearly to stakeholders.
• Strong analytical thinking, problem-solving ability, and attention to detail.
• Good knowledge of Greek and English languages.
• Good knowledge of Microsoft Office tools; familiarity with project management tools and quality management systems (QMS).

What’s in it for you?

• 13th and 14th salary.
• Provident Fund.
• Group Medical Plan.
• Discount scheme.

How to Apply

If you are interested, you can apply via our website: Technology Transfer Scientist Job Details | Remedica Limited

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Technical Skills

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About Company

Remedica Ltd