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QUALITY CONTROL ENTRY-LEVEL ANALYST

S/1,500-1,700/month
Indeed

Company

Job typeFull-time
Workplace typeOnsite
Experience levelNo experience limit
Education levelNo degree limit

Description

Position Summary: Verify the quality of incoming inputs (raw materials and packaging materials) entering the laboratory by performing physicochemical analyses and ensuring compliance with specifications. Key Highlights: 1. Responsible for physicochemical analysis of inputs and raw materials. 2. Assistance in sampling and analysis of primary and secondary packaging materials. 3. Training in GMP, GLP, and preferably ISO 17025:2017. **JOB DESCRIPTION** **1\. JOB OBJECTIVE** Verify that inputs (raw materials and packaging materials) entering the laboratory meet established quality specifications through their analysis. **2\. GENERAL FUNCTIONS AND SPECIFIC RESPONSIBILITIES** * Responsible for conducting physicochemical analyses of inputs. * Sample and analyze raw materials entering the warehouse. * Maintain up-to-date records of raw material sampling. * Assist in sampling and analysis of primary and secondary packaging materials. * Accurately complete records used to perform assigned activities. * Receive, store, and handle input counter-samples. * Review, classify, destroy, and record expired input counter-samples: raw materials and primary packaging materials. * Perform input analyses according to technical specifications and established analytical methodologies. * Sample, analyze, and record water testing assays per the water sampling and analysis program. * Attend general training sessions and internal departmental training on technical topics and the Quality Management System, as well as undergo corresponding evaluations. * Report detected non-conformities or uncertainties to the immediate supervisor. * And other duties assigned by the Quality Control Manager. **JOB PROFILE EDUCATION** * Professional degree and professional registration as a Pharmaceutical Chemist or related field; Bachelor of Pharmacy. **TRAINING** * Knowledge of GMP and GLP * Familiarity with ISO 17025:2017 is preferred * Proficiency in office software * Intermediate-level English language proficiency is preferred * Knowledge of equipment operation **SKILLS** * Planning and organization or Analytical thinking **EXPERIENCE** * Minimum one year of experience in similar positions within the pharmaceutical industry is preferred. Employment type: Full-time Salary: S/.1,500.00 \- S/.1,700.00 per month Work location: On-site employment

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Posted by

María García

Indeed · HR

Location

María García

Indeed · HR

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