Analytical Development Specialist

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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