Lead BP Scientist

Lead British Pharmacopoeia (BP) Scientist

This is a full time, permanent role based in 10 South Colonnade, Canary Wharf London, E14 4PU. Government departments and agencies are working towards implementing a minimum 60% attendance in office sites. We are currently implementing a flexible, hybrid way of working, with a minimum of 8 days per month working on site-up to 12 days depending on business needs. Some roles may require more on site time. Please discuss remote working options with the recruiting manager before accepting an appointment.

What's the role?

The postholder will play a unique role at the MHRA developing legally binding standards and guidance for the British Pharmacopoeia (BP) that protect patients and the public by ensuring medicine quality. You will use your scientific expertise to support the standard setting process from inception through development, publication, and ongoing maintenance. You will work with, manage, and influence external BP Expert Advisory Groups, international stakeholders, and key suppliers to provide the best scientific advice and service delivery.

Key Responsibilities

• Contribute and support the work of the BP Commission, collaborating with colleagues and independent experts to develop and implement appropriate standards and policy for the BP.
• Lead or assist specific scientific or delivery areas/projects to enhance the standards and services provided to users, such as coordinating BP text preparation, developing scientific strategy/policy, and managing recruitment, training, and development activities.
• Advocate for the interests of the BP and Laboratory Services Group through effective communication and joint working with internal and external organizations.
• Support the contract management, performance, and delivery of BP publication and laboratory services suppliers.

Qualifications and Experience

• Degree or equivalent in Biochemistry, Biological Science, Chemistry, Pharmaceutical Chemistry, Pharmacy, or a related scientific discipline.
• Experience applying and developing quality standards for healthcare products.
• Knowledge of analytical techniques and processes used in determining pharmaceutical quality.
• Experience working in a pharmaceutical quality environment or equivalent.
• Broader awareness of trends in life sciences, biopharmaceutical manufacturing, and the regulatory environment, and ability to assess their impact on the pharmacopoeia work.