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- Tasks: Develop and validate analytical methods for drug development in a dynamic R&D environment.
- Company: Join an innovative pharmaceutical company in the stunning South of France, focused on improving patient outcomes.
- Benefits: Enjoy competitive salary, relocation assistance, and a collaborative workplace culture with career growth opportunities.
- Why this job: Be part of a team that values scientific excellence and contributes to impactful healthcare solutions.
- Qualifications: MSc or PhD in relevant fields with 3+ years of experience in analytical development required.
- Other info: Hybrid work model available; French language skills are a plus.
The predicted salary is between 36000 - 60000 £ per year.
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
Analytical Development Specialist employer: Barrington James Limited
Contact Detail:
Barrington James Limited Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Analytical Development Specialist
✨Tip Number 1
Familiarise yourself with the latest advancements in HPLC/UPLC technologies. Being able to discuss recent innovations or techniques during your interview can demonstrate your passion and expertise in analytical development.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those who work in analytical development. Attend relevant conferences or webinars to make connections that could lead to valuable insights or referrals.
✨Tip Number 3
Prepare to discuss specific examples of how you've applied Quality by Design (QbD) principles in your previous roles. This will show your practical understanding and ability to implement these concepts effectively.
✨Tip Number 4
Research our company culture and values to align your responses during the interview. Understanding our commitment to scientific excellence and collaboration will help you articulate why you're a great fit for our team.
We think you need these skills to ace Analytical Development Specialist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in analytical development, particularly with HPLC/UPLC and QbD principles. Use specific examples from your past roles to demonstrate your expertise.
Craft a Compelling Cover Letter: Write a cover letter that connects your skills and experiences directly to the job description. Emphasise your hands-on experience in method development and validation, and express your enthusiasm for working in the pharmaceutical industry.
Highlight Regulatory Knowledge: Since the role requires knowledge of ICH guidelines and regulatory submissions, make sure to mention any relevant experience you have in these areas. This will show that you understand the compliance aspects of the job.
Proofread Your Application: Before submitting, carefully proofread your application materials for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in analytical development.
How to prepare for a job interview at Barrington James Limited
✨Showcase Your Technical Expertise
Be prepared to discuss your hands-on experience with HPLC/UPLC systems in detail. Highlight specific projects where you developed or validated analytical methods, and be ready to explain the challenges you faced and how you overcame them.
✨Demonstrate Knowledge of QbD Principles
Since the role emphasises Quality by Design, make sure you can articulate how you've applied QbD principles in your previous work. Discuss any relevant case studies or examples that illustrate your understanding of method robustness and lifecycle management.
✨Prepare for Regulatory Discussions
Familiarise yourself with ICH guidelines and global regulatory requirements. Be ready to discuss how you have supported regulatory submissions in the past, and prepare to answer questions about your experience in GMP/GLP environments.
✨Emphasise Collaboration Skills
This position requires cross-functional collaboration, so be prepared to share examples of how you've worked effectively with teams from different departments. Highlight your communication skills and any mentoring experiences you have had with junior scientists.
