• Organise the laboratory equipment prior to water analysis• Assist in the analysis of the raw material (water) through the Dissolved organic carbon analysis (DOC, LC-OCD - Liquid chromatography – Organic Carbon Detection) • Prepare the mobile phase and solutions used in analysis • Prepare the dilutions of water samples for the DOC, LC-OCD & ICP equipment• Assist in the cleaning and sterilization of equipment including glass vials.• Disposal of both Halogenated and non-Halogenated waste • Organize and change all gases cylinder

• Storing of products in the right shelves and processing sales at the cash register• Helpful with Pharmacist• Webster Pack Assistant - Every week, the assistants packed medication into blister packs for patients to reduces the risk of dosage compliance problems and helps people obtain the maximum benefit from their medicines. Each dose for each time of the day is sealed in a separate compartment.

• Analysis of the raw material, active principles and finished products through the equipment such as: (HPLC / ICP / Spectrophotometer / Atomic Absorption) for analysis of Content, Identification, Dissolution, Uniformity, • Planning and purchasing of standards for use in the laboratory• Management and optimization of the inventory referent to standards solutions as checking expiry dates of the mobile phase as a member of the Yellow Belt Project• Management of the mobile phase used in analysis such a hormonal products and quality• control;• Knowledge of Systems: LIMS, SAP and Empower;• Elaboration of a standard operating procedure and implementation of corporate policies following the Good Manufacturing Practice(GMP);• Experience in the process of Corporate Inspection, VISA, INVIMA and ANVISA.• Experience in training and organization of teams, ease of working in groups;

• Assist clinical research associates and regulatory team, monitoring in hospitals and research centers supporting, updating and maintaining clinical documents and system;• Support with clinical team on the preparation, accounting, distribution and archiving of clinical documentation;• Assist with periodic review of study file, collaborating and maintenance of tracking information;• Working relationships with clinical team for designated project communications; • Assist project teams with study specific documentation and guidelines as appropriate;• Set up, organize and maintain clinical study documentation;• Support company goals and objectives, policies and procedures, Good Clinical Practices, and FDA regulations;

• Assist in the cleaning and sterilization of equipment, calibrate, and carry out routine maintenance of the Laboratory equipment, through pre-established methods;• Analysis of the raw material, active principles and finished products through the equipment such as: (Spectrophotometer / Atomic Absorption) for analysis of Content, Identification, Dissolution, Uniformity;• Knowledge of Systems: SAP;• Elaboration of a standard operating procedure and implementation of corporate policies following the Good Manufacturing Practice (GMP);• Experience in the process of Corporate Inspection, VISA, INVIMA and ANVISA;• Prepare, implement, review and evaluate documents (monographs, general methods).. Report and provide detailed information related to consumers feedback and complaints to the pharmacovigilance department, regulatory affairs, sales team, and marketing.. Assist sales representatives in the field (pharmacy and clinics).