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DescripciónDescription
Develop and optimize manufacturing processes for pharmaceutical products, ensuring the quality and safety of final products.
Perform laboratory tests on raw materials, intermediates, and finished products to ensure they meet quality specifications.
Collaborate with the Quality Control team in implementing analytical methods and process validation procedures.
Analyze and evaluate experimental data, creating detailed technical reports for internal teams and regulatory authorities.
Ensure compliance with local and international regulations related to pharmaceutical manufacturing (such as GMP, FDA, EMA, etc.).
Manage and maintain technical documentation for pharmaceutical products, ensuring traceability and regulatory compliance.
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Requisitos Requirements
Bachelor's degree in Pharmaceutical Chemistry, Chemistry, Chemical Engineering, or a related field.
Minimum of [2] years of experience in the pharmaceutical industry, preferably in research and development (R&D) or quality control.
Knowledge of Good Manufacturing Practices (GMP), FDA, EMA, and other pharmaceutical industry regulations.
Proficiency in analytical techniques such as high-performance liquid chromatography (HPLC), mass spectrometry (MS), and others.
Knowledge of specialized laboratory software for data analysis and documentation management.
Ability to work in multidisciplinary teams and communicate effectively with other departments.
Commitment to quality, safety, and regulatory compliance standards.
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