Key roles and responsibilities:

• Lead analytical method transfer, verification, qualification and validation activities to support new product introductions within GMP QC laboratories.
• Identify analytical risks and develop effective mitigation strategies to support successful project delivery.
• Drive continuous improvement of analytical lifecycle management, QC readiness activities and method transfer processes.
• Develop and maintain analytical project plans, ensuring milestones and deliverables are achieved on schedule.
• Ensure QC laboratory readiness, including analytical methods, specifications, equipment, reference standards, reagents, training and supporting documentation.
• Act as the primary Analytical QC representative within multidisciplinary project teams and serve as the QC lead for assigned product introduction programmes.
• Provide scientific expertise to solve complex analytical and technical challenges.
• Ensure compliance with cGMP, GxP, ICH guidelines, Quality Management Systems and all applicable regulatory requirements.
• Promote a strong quality culture across the team, reinforcing that quality is everyone's responsibility.

Requirements:

The following experience and qualifications are essential for success in this role:

• Degree or equivalent qualification in Chemistry or a related scientific discipline.
• Significant industrial laboratory experience, ideally gained over at least eight years within a regulated environment.
• Strong expertise in analytical chemistry and the application of analytical and physical science techniques to solve complex challenges.
• In-depth knowledge of analytical lifecycle management and method transfer into GMP Quality Control laboratories.
• Experience leading analytical method development, transfer, qualification and validation activities.
• Experience authoring and reviewing protocols, reports and technical documentation.
• Understanding of GMP, GxP and ICH regulatory requirements.
• Proven ability to lead teams and manage multiple priorities effectively.

Why Pharmaron?

Collaborative Culture: Thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners and collaborators.

How to Apply:

Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!

Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.