Analytical Development Specialist

Barrington James; United Kingdom; Hybrid; GBP 40,000 - 80,000; Full time

Job summary

Join a dynamic pharmaceutical company in the South of France as an Analytical Development Scientist or Senior Scientist. In this hybrid role, you will develop and validate analytical methods crucial for drug development. The position emphasizes strong expertise in HPLC/UPLC and Quality by Design principles, allowing you to contribute significantly to innovative projects. Enjoy a collaborative workplace culture, competitive salary, and the chance to live in one of Europe's most beautiful regions. This opportunity is perfect for driven individuals looking to make a real impact in the pharmaceutical industry.

Benefits

Competitive salary

Relocation assistance

Collaborative workplace culture

Career development opportunities

Qualifications

• 3+ years of experience in analytical development for Scientist role.
• 6+ years of experience in analytical development for Senior Scientist role.

Responsibilities

• Develop and validate analytical methods for drug substances and products.
• Collaborate with cross-functional teams to ensure method robustness.

Skills

HPLC

UPLC

Quality by Design (QbD)

Analytical Method Development

Regulatory Compliance

GMP/GLP Environments

Communication Skills

Education

MSc in Analytical Chemistry

PhD in Pharmaceutical Sciences

Tools

Empower Software

Job description

Job Title: Analytical Development Scientist / Senior Scientist
Location: South of France
Industry: Pharmaceutical
Job Type: Hybrid

About Us:
We are a dynamic and innovative pharmaceutical company based in the beautiful South of France, dedicated to developing high-quality medicines that improve patient outcomes worldwide. With state-of-the-art facilities and a strong emphasis on scientific excellence, we are expanding our Analytical Development team and are seeking a talented and driven Scientist or Senior Scientist to join us.

Position Summary:
As part of our R&D division, you will play a key role in developing and validating robust analytical methods to support drug development across various phases. This role requires a hands-on expert with strong experience in HPLC/UPLC, Quality by Design (QbD) principles, and regulatory-compliant method development and validation.

Key Responsibilities:

• Develop, optimize, and validate analytical methods (HPLC/UPLC, dissolution, etc.) for drug substances and drug products in line with ICH guidelines.
• Apply QbD principles in method development to ensure method robustness and lifecycle management.
• Prepare method validation protocols and reports, and ensure methods are transfer-ready for QC or manufacturing sites.
• Conduct forced degradation studies and stability-indicating method development.
• Troubleshoot and resolve analytical issues proactively.
• Collaborate cross-functionally with formulation, manufacturing, regulatory affairs, and quality assurance teams.
• Maintain detailed documentation and support regulatory submissions (IND, IMPD, NDA, etc.).
• Mentor junior scientists and support technical training where needed.

Required Qualifications:

• MSc or PhD in Analytical Chemistry, Pharmaceutical Sciences, or a related field.
• Minimum 3+ years (Scientist) or 6+ years (Senior Scientist) of industry experience in analytical development.
• Proven hands-on expertise with HPLC/UPLC systems (Empower preferred), method development, and validation.
• Solid understanding and application of QbD concepts and risk-based approaches.
• Strong knowledge of ICH, USP/EP, and relevant global regulatory requirements.
• Experience in working within GMP/GLP environments.
• Excellent communication skills in English; French proficiency is a plus.

What We Offer:

• Competitive salary and benefits package
• Relocation assistance (if applicable)
• A collaborative and inclusive workplace culture
• Career development opportunities in a growing international organization
• The opportunity to live and work in one of Europe's most desirable regions

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