At Target Healthcare Group, we are pioneers in the pharmaceutical industry, committed to revolutionising healthcare. As the UK’s leading manufacturer and supplier of unlicensed medicines and hard-to-source products, we serve retail pharmacies, hospitals, pharmaceutical wholesalers, and homecare markets with unmatched expertise and passion.
With a diverse team of over 500 professionals, including top pharmacists, skilled technicians, and dedicated support staff, we ensure excellence and innovation in everything we do.

THE ROLE

We are looking for a detail-oriented technology transfer specialist, knowledgeable in GMP manufacturing, validation and quality control. You will be an integral part of cross functional project teams including Manufacturing, QC, QA, Supply Chain and Project Management to progress commercialisation of an array of pharmaceutical products.

AS A TECHNOLOGY TRANSFER SPECIALIST YOUR RESPONSIBILITIES WILL INCLUDE, ALTHOUGH NOT LIMITED TO:

• Support the transfer of new processes into GMP manufacturing facilities and quality control working closely with internal and external teams.
• Participate in discussions with CMOs to support on-boarding of new projects and technologies into internal and external sites.
• Complete process and facility gap assessments for new processes and work collaboratively with the Project Manager to generate a robust process transfer plan.
• Agree and generate final process descriptions.
• Write and review process change controls, validation protocols, risk assessments, batch records and other relevant documentation for both ongoing and new manufacturing processes.
• Develop new technical protocols, SOPs, and related technical documentation to support technology transfer and ongoing development of manufacturing projects.
• Complete GMP material assessments and finalise bills of materials.
• Support evaluation and adoption of manufacturing equipment or technologies.
• Provide specialist training to manufacturing and analytical staff supporting the introduction of new products, processes, changes, and improvements.
• Support (as SME) technical investigations and out of specifications generating, reviewing, and approving technical reports to support timely close-out of QMS.
• Support the troubleshooting of process excursions/out of trends as required.
• Communicate findings and recommendations to stakeholders through presentations and reports.

TO BE SUCCESSFUL IN THIS ROLE, YOU SHOULD BE ABLE TO DEMONSTRATE:

• Minimum of 2+ years hands on GMP manufacturing, validation or quality control experience.
• Bachelor’s or Master’s degree in a relevant field such as Life Sciences, Chemistry, Pharmacy, Engineering Physics, or Technology Management.
• Experience in technology transfer and commercialisation, or a related field.
• Excellent analytical skills.
• Strong project management skills with the ability to contribute to multiple projects simultaneously.
• Excellent communication and negotiation skills for liaising between industry partners.
• Knowledge of regulatory and compliance considerations related to technology transfer and GMP manufacture.
• Strong determination to solve problems.
• Can-do attitude.
• Good organisational skills