Senior R&D Analyst
Lavipharm
Πλήρης απασχόλησηLavipharm is seeking Senior R&D Analyst who will be responsible for independently developing and validating analytical methods and improving existing methodologies. The role also involves executing laboratory analyses and experiments to support pharmaceutical development programs. This position requires expertise in handling, analyzing and characterizing chemicals, pharmaceuticals, and related molecules/reagents.
The ideal candidate will possess substantial hands-on experience with advanced analytical techniques, such as High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), dissolution apparatuses, etc., to accurately analyze and characterize pharmaceutical substances and products in compliance with regulatory guidelines. The Senior R&D Analyst will demonstrate proficiency in method development and validation to support drug product development and manufacturing processes.
Job position reports to Lead R&D Analytical.
Responsibilities- Develop and validate analytical methods or enhance existing ones with minimal supervision.
- Apply advanced scientific principles, theories, and concepts to resolve analytical challenges related to drug products, ensuring compliance with applicable regulatory guidelines.
- Design and execute non-routine experiments independently, addressing complex research questions.
- Monitor the stability program of in-development products and perform required stability analyses.
- Accurately analyze experimental data, interpret outcomes, and propose appropriate follow-up actions.
- Conduct literature searches and extract relevant scientific information from protocols, journals, and publications.
- Maintain comprehensive knowledge of regulatory requirements (ICH, EMA, or other relevant authorities) and ensure their appropriate application in research projects.
- Manage various aspects of analytical projects with minimal supervision, ensuring timely progress and quality.
- Provide project updates and communicate findings effectively when required.
- Author technical documentation, including analytical test methods, development reports, and validation protocols, with a high level of scientific accuracy.
Education:
• Bachelor of Science (BSc) in Chemistry, Pharmacy, or other relevant Health Sciences disciplines.
• Master of Science (MSc) in Analytical Chemistry, Industrial Pharmacy, Chemistry, Chemical Engineering, Biochemistry, or a related field is preferred.
Experience:
• A minimum of 1-2 years of experience in pharmaceutical analysis.
• Practical expertise with analytical instrumentation, including HPLC, GC, UV-Vis spectrophotometry, and dissolution testing.
• Prior experience with analytical method validation and technical documentation is an advantage.
Skills:
• Proficiency in Microsoft Office Suite, with a focus on Excel and statistical tools (e.g., Minitab or equivalent).
• Excellent data interpretation, problem-solving, and scientific writing skills.
• Strong familiarity with regulatory guidelines (ICH, EMA, etc.).
• Excellent command of the English language, both written and verbal.
This position offers an opportunity to contribute to cutting-edge pharmaceutical research in a collaborative and dynamic environment. If you are driven by innovation and possess the required skills, we invite you to join our team.
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