Director - Pharma

JR United Kingdom; Liverpool; On-site; GBP 70,000 - 100,000; Full time

Job summary

Join JR United Kingdom as a Lead for the Manufacturing Science and Technology team in Liverpool. This pivotal role involves driving technical excellence across a diverse product portfolio, overseeing product lifecycle management, and leading strategic improvements in biopharmaceutical manufacturing. You will shape technical strategy and develop future talent, ensuring high performance across operations.

Qualifications

• Significant experience in technology or biopharmaceutical process development.
• At least 5 years in a leadership role in biopharmaceutical manufacturing.
• Strong knowledge of GMP, ICH guidelines, and global validation standards.

Responsibilities

• Lead site technical strategy for product lifecycle management and new product introductions.
• Act as a strategic partner on the site leadership team.
• Ensure product performance and regulatory compliance.

Skills

Leadership

Strategic Planning

Regulatory Compliance

Process Optimization

Stakeholder Engagement

Job description

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We are seeking a dynamic and experienced Lead for the Manufacturing Science and Technology (MSAT) team at our Barnard Castle site. This is a pivotal leadership role responsible for driving technical excellence across a diverse product portfolio, including sterile manufacturing, clean liquids, and dermatological products. You will play a key role in supporting new product introductions, overseeing product lifecycle management, and leading strategic improvements to existing supply chains.

As a member of the site leadership team, you will shape technical strategy, develop future talent, and ensure high performance across technical operations. Your remit includes championing technical governance processes, ensuring robust product lifecycle oversight, and collaborating cross-functionally to resolve complex manufacturing challenges. You’ll also represent Barnard Castle within the wider MSAT community and contribute to global strategic initiatives.

Key Responsibilities:

• Lead site technical strategy for product lifecycle management, new product introduction, and technology transfers.
• Act as a strategic partner on the site leadership team, aligning with cross-functional leaders to drive business goals.
• Ensure product performance, process optimization, and regulatory compliance through effective technical oversight.
• Resolve technical issues impacting supply using robust RCA and CAPA frameworks.
• Build a high-performing team through proactive talent management and capability development.

Why You?

Basic Qualifications:

• Significant experience in technology or biopharmaceutical process development, tech transfer, and manufacturing operations.
• At least 5 years in a leadership role in biopharmaceutical/biotech manufacturing.
• Experience with product registration and regulatory engagement (FDA/EMEA).
• Strong knowledge of GMP, ICH guidelines, and global validation standards.

Preferred Qualifications:

• Proven leadership with strong interpersonal and stakeholder engagement skills.
• Ability to influence across scientific, engineering, quality, and operational disciplines.
• Skilled in communication, decision-making, and strategic planning.

Join us and lead innovation and technical excellence at one of client’s flagship manufacturing sites.