Job Requisition ID: 32602
Department: Prod. - Gen. (101)
Category: Production
Location:Wales
Date: 1 Sept 2025

Our Purpose is supported by our 4 key values:

• We make patients our priority
• We act with integrity and accountability
• We work together as one team
• We look for better ways forwar

Principle Responsibilities

• Provide technical input into validation activities for the Production team – write, review, approve and execute studies as required.
• To perform administrative tasks and provide rapid issue resolution for all electronic manufacturing systems, including EAMS, MES and computerized processing equipment controlling systems.
• Work alongside internal & external functions to transfer new equipment and techniques effectively & efficiently to production scale.
• Active participant for site Operational Excellence initiatives. To foster and encourage Continuous Improvement within the Production department. Lead process improvement initiatives and activities to influence change.
• To actively maintain and update knowledge and expertise of current developments, standards and operating practices within the biotechnology and pharmaceutical industries
• Input into the Regulatory strategy and author the relevant sections of Regulatory dossiers to support both Changes & Deviations.
• Ensure practical training modules are in place so that new starters within the teams are provided with sufficient background understanding and knowledge before entering into their roles. Responsible for the provision of training to new starters and for robust re-training modules to maintain a high compliance within the teams.
• Provide subject matter expert input to Regulatory, internal and external audits.
• Cover operator absence within the facility as required.
• Ensuring that all interactions and engagements are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with BTG values.
• Carry out other reasonable tasks as required by the Line Manager