Principal Scientist

JR United Kingdom; England; On-site; GBP 60,000 - 90,000; Full time

Job summary

A leading company in pharmaceutical development is seeking a (Senior) Principal Scientist in Analytical Science. This role involves driving analytical science projects, mentoring junior staff, and ensuring compliance with global regulatory standards. The ideal candidate will have a PhD or extensive experience in drug development and a strong understanding of regulatory requirements.

Qualifications

• PhD with over 5 years’ experience or bachelor’s degree with over 10 years’ experience in pharmaceutical sciences.
• Experience in progressing analytical components of drug projects.
• Good understanding of ICH quality guidelines and global CMC regulatory requirements.

Responsibilities

• Guide the development of analytical methods for drug products.
• Communicate global regulatory requirements for CMC submissions.
• Lead or manage pharmaceutical development projects for clients.

Skills

Team collaboration

Communication

Project leadership

Influencing

Education

PhD in pharmaceutical sciences

Bachelor's degree in pharmaceutical sciences

Job description

Job Description – (Senior) Principal Scientist, Analytical Science

Job Title:

(Senior) Principal Scientist – Analytical Science

Department:

Pharmaceutical Development

Line Manager:

Team Director

Location:

South Manchester (occasional travel required for client meetings, CRO visits, and business development events across the UK and potentially abroad. Occasional overnight stays may be necessary.)

Job purpose:

The primary purpose of this role is to ensure excellence in the Client’s analytical science provision. You will be responsible for driving analytical science and regulatory components of client projects, as well as mentoring junior analytical staff.

You will stay updated with the latest advances in analytical science and introduce relevant technologies into the business.

As a senior team member, you will support business growth by providing technical consultancy, scientific guidance, and support for business development activities.

Typical responsibilities/accountabilities:

1. Guide the development of fit-for-purpose analytical methods for various drug products and troubleshoot development issues.
2. Understand and communicate global regulatory requirements for CMC submissions and design product strategies accordingly.
3. Combine scientific and pragmatic design thinking to deliver solutions for client compounds and products.
4. Ensure the client has the necessary analytical expertise and capabilities, including the adoption of new technologies.
5. Provide hands-on troubleshooting for complex analytical challenges.
6. Lead or manage pharmaceutical development projects for clients.
7. Manage and review CRO activities on behalf of clients.
8. Handle financial and contractual aspects of projects, such as proposals and invoicing.
9. Serve as a key contact for the client’s global customer base.
10. Author SOPs and best practices documents, and continuously improve analytical capabilities.
11. Participate and present at conferences and network events.
12. Provide direction, oversight, and coaching to staff.
13. Perform other activities aligned with your role and company status.

Education, Qualifications, Experience, Skills, and Capabilities:

1. PhD with over 5 years’ experience or bachelor’s degree with over 10 years’ experience in pharmaceutical sciences and drug development.
2. Experience in progressing analytical components of drug projects through development phases across global markets.
3. Experience interacting with global regulatory authorities.
4. Good understanding of ICH quality guidelines and global CMC regulatory requirements.
5. Strong team collaboration skills.
6. Ability to meet deadlines and targets.
7. Excellent communication and presentation skills.
8. Influencing skills.
9. Project leadership experience.
10. Self-motivated and independent worker.
11. Commitment to self-development and learning.