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Technology Transfer Scientist

Job in Penicuik, Midlothian county, EH26, Scotland, UK
Listing for: AliveDx
Full Time position
Listed on 2026-08-09
Job specializations:
  • Pharmaceutical
    Quality Engineering, Validation Engineer
Salary/Wage Range or Industry Benchmark: 42000 - 65000 GBP Yearly GBP 42000.00 65000.00 YEAR
Job Description & How to Apply Below

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At Alive Dx, we empower diagnostic insights, transform patient care, and innovate for life. With over 30-years in in-vitro diagnostics, we put the health of patients first by creating innovative solutions designed for faster diagnostic results. Alba–– our blood bank reagents portfolio–– and MosaiQ®–– one of the first multiplexing and multimodality automated testing platforms––are designed to make labs more efficient and clinical decision-making more effective.

Our journey started as Alba Bioscience, and later, Quotient. Today, as Alive Dx, we innovate for life.

TECHNOLOGY TRANSFER SCIENTIST

Alive Dx is recruiting for a Technology Transfer Scientist to join the Manufacturing Technical Implementation team based in Penicuik, Scotland. The role is a full-time, permanent position working Monday to Friday with flexible working arrangements where applicable.

As a Technology Transfer Scientist, you will play a key role in bridging Research & Development and Manufacturing, ensuring the successful transfer of new products, processes and technologies into routine manufacturing. Working cross-functionally, you will lead technology transfer activities, support validation programmes and e nsure manufacturing processes are implemented efficiently while meeting GMP and regulatory requirements.

YOUR MISSION

Your main responsibilities will include:

  • Leading technology transfer projects for new products, manufacturing processes and equipment.
  • Planning, coordinating and driving technology transfer activities with cross-functional stakeholders.
  • Developing and presenting technology transfer strategies and project plans.
  • Leading the preparation and execution of validation batches and providing technical guidance to the relevant teams.
  • Creating and managing GMP documentation including manufacturing protocols, validation protocols, process maps, final product specifications and BMR's.
  • Analysing process data and quality control results to support successful process implementation.
  • Managing Non-Conformances, CAPAs and Change Controls associated with technology transfer activities.
  • Reporting project progress against agreed timelines while ensuring effective communication across departments.
  • Supporting continuous improvement initiatives and contributing to new manufacturing-based projects.
YOUR COMPETENCIES
  • A degree in Life Sciences, Engineering or a related scientific discipline or equivalent experience
  • Experience working within a GMP-regulated pharmaceutical, biotechnology or medical device environment.
  • Knowledge in Blood Grouping Reagents, products and processes
  • Experience in process development, manufacturing technical support or technology transfer.
  • Excellent project planning, organisational and stakeholder management skills.
  • A proactive, flexible approach with the ability to manage competing priorities and tight deadlines.
WHAT WE OFFER
  • A highly dynamic and growing environment.
  • An opportunity to live your passion for intrapreneurial mindset, where cultivating innovation and customer centricity are at the heart of everything we do.
  • A flexible working environment where applicable and a range of core and flexible benefits ranging from private medical cover, life assurance, additional annual leave, cycle to work, technology, experience days and access to marketplace discounts.

Alive Dx is an equal opportunity employer and welcomes applications from all qualified individuals regardless of nationality, sex, disability, region/belief, sexual orientation or age. All aspects of employment including the decision to hire, promote, discipline, or discharge, will be based on competences, performance and business needs.

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