Irina Kinyaeva

Experience

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  PepsiCo

  Feb 2013 - May 2013

  Chemist

  Analytical work;- Conducting chemical analysis and research;- Maintenance of appropriate records;- Calibration of equipment and instrumentation;- Control of physical and chemical parameters of syrups and drinks;- Quality control markings and labels;- Monitoring of Laboratory health status;- Preparation of standard solutions;Work with equipment (spectrophometer, laboratory water purification system, pH Meter, fume hood, carbo QC, densitometr, titrator, turbidimetr, manometers, thermometers) Show less

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  Nestlé, NQAC (Nestle quality assurance center)

  Jun 2013 - Mar 2017

  Chemist

  Conducting chemical-physical and chemical-toxicological analyzes of safety and quality of raw materials and finished products.Putting into practice elements of the quality system Nestle (GLP, NCE, NQMS).Participation in audits of factory laboratories Nestle Group.Participation in international comparison tests.Conducting tests collation factory laboratories Nestle Group.Validation and verification methods.Education specialists of factory laboratories and new employees of the central laboratory.Work experience in a wide range of analytical equipment (gas chromatography with FID, FPD, ECD, MS detectors; GPC; soxhlet; extractors; autotitrator etc.). Maintenance of equipment, establishment of working methods, selection conditions, standardize equipment, equipment calibration.Examination of samples on the following parameters: pesticides, fatty acid composition, fats, proteins, carbohydrates, moisture, ash, nitrates, vitamin C, fiber, beta-glucan, peroxide value, iodine value, acidity, antibiotics. Show less

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  Stentex LLC

  Mar 2017 - now

  Quality Engineer (Supplier Quality and Receiving Inspection)

  Record keeping in accordance with the QMS;Verification and harmonization of procedures related to the SQE and RI according to functional or other characteristics;Coordination of contracts with counterparties;Evaluation and control of the budget of the RI laboratory;Purchase of furniture, equipment, reagents, dishes. Payment of bills in 1C;Documenting the receiving inspection to ensure that the quality of incoming materials meets the standards and specifications in the SAP system. Drawing up a sampling plan;Timely implementation of the required measures to investigate nonconformities and eliminate deviations;Work with suppliers on issues of complaints and inconsistencies;Installation and maintenance of equipment. Ensuring timely verification and calibration of equipment;Training of new employees of the laboratory;Interaction with the production team, suppliers, employees of the planning department and other departments, functionally related to the activities of the supplier assessment and input control group;Conducting regular inspections in the warehouse and quarantine / reject area;Evaluation and selection of suppliers;Conducting external audits for compliance with GOST ISO 9001, GOST ISO 17025 and the requirements of the Quality Agreements;Evaluation of the effectiveness of suppliers' corrective actions based on the results of the audit;Analysis of discrepancies in the quality of purchased products: a request to analyze the causes of deviations and corrective action plans;Development and coordination of Quality Agreements with suppliers.Projects:Designing RI laboratory.Progress:Passage of audit at GOST ISO 13485 Medical products. Quality management systems. System requirements for regulatory purposes without comment;Establishing an RI process;Establishment of the precursors accounting process. Show less