Tech Transfer Engineer (Biopharma)

Description

• Share best practices and support continuous improvement initiatives across the site.
• Provide technical support for Drug Product operations such as formulation, filling, lyophilisation, capping and automated visual inspection.
• Act as process owner for assigned areas, demonstrating technical expertise and ensuring robust, compliant processes.
• Support technology transfer activities by preparing, reviewing and executing GMP documentation, including master batch records, protocols, reports and change controls.
• Support Commercial and Technology Transfer activities through on-the-floor technical assistance and person-in-plant engagement.
• Analyse process performance using statistical tools and identify opportunities for improvement, optimisation and standardisation.
• Ensure compliance with GMP requirements and regulatory expectations, collaborating closely with Operations, Quality and Regulatory functions.
• Lead or support investigations, atypical event assessments and root-cause analysis, ensuring effective CAPA development and implementation.
• Contribute to inspection readiness activities and participate in audits as required.

Requirements

• Bachelor’s degree in Chemical/Biochemical Engineering, Pharmaceutical Sciences, Chemistry, Biology or related field.
• Minimum 3 years’ experience in a GMP environment within operations, engineering, technical operations, MS&T, or a similar function.
• Experience in aseptic operations, process development, analytical support or technology transfer.
• Knowledge of regulatory frameworks such as Annex 1 and relevant industry guidance.
• Proficiency in statistical tools for process monitoring and continuous improvement.
• Background in deviation management, change control, equipment support or qualification.
• Experience with lyophilised products and start-up or scale-up environments.

Benefits

Training + Development

Interview process

Visa Sponsorship

Security clearance