Analytical Development Analyst

The contractor will be responsible for developing and validating analytical methods for the quality control of pharmaceutical products. They will also contribute to release and stability testing of raw materials, intermediates, drug substances, and finished products.

The role requires effective teamwork under the supervision of a scientist. Team size may vary depending on the project. The contractor will collaborate with Chemical Process Research & Development and Drug Delivery Design & Development teams within the Pharmaceutical Sciences Department.

The contractor is expected to work autonomously and proactively, while consulting with the supervising scientist for decision-making. Creativity is required, particularly when developing new analytical methods.

• Perform analyses of raw materials, intermediates, bulk products, and finished packaged products in accordance with work instructions and established procedures (stability studies, in-process controls, clinical release, investigations, etc.).
• Develop and validate analytical methods to support projects across different phases of product development.
• Conduct stability studies and clinical release testing for Phase I and II clinical trials, as well as analyses supporting process understanding (IPC tests, forced degradation studies, multimedia dissolution, etc.).
• Analyze results critically and ensure consistency with previously generated data where applicable.
• Participate in the transfer of analytical methods to Quality Control (QC) and subcontractors.
• Manage and maintain documentation related to laboratory activities using relevant software systems (e.g., GLIMS, eNoval, Veeva).

Quality Responsibilities

• Ensure all necessary information and instructions are received and understood before starting any task.
• Follow procedures rigorously and report any deviations to the responsible person.
• Use only authorized and validated analytical methods.
• Properly use and maintain analytical equipment and laboratory facilities.
• Perform peer review and double-checking within the team.

• Bachelor’s or Master’s degree in Analytical Chemistry.
• 3 to 5 years of relevant professional experience.
• Strong technical expertise in small molecule chromatography (HPLC/UHPLC/GC) and detection techniques (UV/Vis, RI, MS).
• Good knowledge of USP/EP Pharmacopoeias.
• Key competencies: strong team player, experience in a similar environment, high level of rigor and compliance, with a clear understanding of the importance of strictly following procedures.

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