Analytical Development Specialist
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* This role plays a crucial part in ensuring the quality and compliance of pharmaceutical compounds by developing and validating robust analytical techniques in line with ICH and GMP standards.
* You will be responsible for method development and validation, documentation and reporting, supporting QC and In-Process Controls (IPC), and method testing and optimization.
Main Responsibilities:
1. Develop and validate analytical methods using HPLC, UPLC, and GC.
2. Troubleshoot and optimize analytical methods to improve reliability and performance.
3. Draft validation protocols for review by research chemists and QA.
4. Compile validation reports summarizing procedures, parameters, results, chromatograms, and conclusions on method suitability.
5. Ensure documentation complies with GMP standards.
6. Collaborate closely with research chemists and serve as a link between analytical development, QC, and R&D teams.
7. Conduct experimental tests to support method development and validation.
8. Aess and refine analytical methods based on internal and client-defined acceptance criteria.
9. Work in partnership with clients to meet specific project requirements.
Your Profile:
* Educational background in chemistry, pharmaceutical sciences, or a related field (Masters' or equivalent preferred).
* Experience in analytical method development and validation in a GMP-regulated environment.
* Hands-on experience with chromatographic techniques and software.
* Strong documentation, organizational, and communication skills.
* Ability to troubleshoot technical issues and optimize methods effectively.
* A team player with a proactive mindset and attention to detail.
Benefits:
* Permanent contract
* Salary package in line with your experience
* Extra benefits (company car, meal vouchers, recovery days, insurances)
What We Offer:
* The possibility to join a great team
* Be part of the success story of an international group