Technical Team Leader

JR United Kingdom; Stirling; Hybrid; GBP 80,000 - 100,000; Full time

Job summary

An innovative life science organization is seeking a skilled Technical Team Leader to drive new projects and enhance production processes. This exciting role involves managing a team, supporting the introduction of new projects, and ensuring compliance with quality standards in a GMP-regulated environment. With a focus on technical transfer and process improvement, you'll play a key role in shaping the future of advanced therapies. The position offers the flexibility of hybrid working arrangements after initial training, making it a fantastic opportunity for professionals looking to make a significant impact in the life sciences sector.

Qualifications

• Experience in GMP regulated and/or pharmaceutical production is essential.
• Extensive experience working with steriles and aseptic production required.

Responsibilities

• Support the Head of Technical and manage Technical Supervisors.
• Ensure quality standards are achieved and maintained in production.
• Oversee technical transfer processes and project introductions.

Skills

Technical Transfer

Process Improvement

Line Management

GMP Regulations

Aseptic Production

Customer Facing Experience

Education

Relevant Scientific Degree

Job description

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SRG are working with a growing life science organisation to help them expand their team.

If you are an experienced Technical Team Leader or Senior Production professional with experience of technical transfer and/or new process introduction, then this could be the perfect next step for you.

The role also offers hybrid working longer term after initial training.

The role:

• Provide direct support to the Head of Technical
• Liaise with the Head of Technical in the introduction of new projects
• Line management of Technical Supervisors
• Support transfer of new projects
• Responsible for scheduling the Technical Supervisors in technical and manufacturing activities
• Support with procurement for materials required for production of batches
• Technical approval of BMRs
• Technical assessments of APIs and drug substances
• Generation of raw material specification writing
• Process improvement of technical transfer processes
• Training in technical expertise
• Ensure that quality standards are achieved and maintained by taking ownership of non-conformances and CAPA’s as required and ensure that QMS documents are completed in a timely manner

Requirements:

• A relevant scientific degree would be preferred or equivalent experience
• Experience in GMP regulated and/or pharmaceutical production
• Extensive experience working with steriles and aseptic production
• Experience of working in a cleanroom environment
• Customer facing experience would be advantageous
• Experience working in formulation would be beneficial
• Experience of working within the field of advanced therapies would be highly beneficial
• Line management experience would be preferred

If you meet the above requirements, then please apply online to find out more!