Maryna Jvr

Quality Officer

Solenis • Tiempo completo

May 2024 - Present • 2 yrs 4 mos

QCQA Officer responsible for implementing, monitoring, & continuously improving QMS to ensure product compliance, regulatory adherence, & operational excellence within a FMCG chemical manufacturing environment. Key Responsibilities -Implement & maintain QMS aligned with ISO 9001, GMP, & internal company standards. -Ensure compliance with chemical manufacturing regulations, SABS requirements, SHEQ policies, & customer specifications across raw materials, in‑process production, & finished goods. -Conduct internal audits & compliance inspections; document findings & manage CAPA -Manage NCRs & perform RCAs to drive continuous improvement & risk reduction. -Control & maintain quality documentation including SOPs, specifications, & quality records. -Monitor trends (SPC charts) to reduce defects, rework, & quality-related deviations. -Compile & deliver daily quality reports to management, summarizing quality performance & results from the previous 24hrs. -Provide system oversight of lab testing, ensuring data integrity, method compliance, & alignment with quality system requirements. -Plan, implement, & oversee verification & validation studies; evaluate study data & prepare technical reports for management review. -Lead lab method development & method improvement to increase accuracy, reliability, & fitness for purpose of test results. -Identify, source, & manage the installation of new laboratory equipment to improve analytical accuracy, repeatability, & reporting confidence. -Oversee supplier quality assurance, including supplier evaluations, incoming goods inspections, & quality performance monitoring. -Investigate & resolve customer complaints, ensuring effective corrective actions & timely close‑out. -Support external audits, regulatory inspections, & customer audits through preparation, facilitation, & follow‑up actions. -Collaborate cross‑functionally with production, SHEQ, R&D, procurement, & logistics to ensure consistent product quality & regulatory compliance.

Laboratory Manager

Krome Metal Chemicals • Tiempo completo

Jan 2023 - May 2024 • 1 yr 4 mos

My core responsibility is to maintain the laboratory management system. This involves: -Team Management: Overseeing lab operations -Quality Control & Compliance: Implement & enforce stringent QC measures to ensure that all products manufactured meet the required specifications & comply with safety standards & regulations. -R&D: Lead & support R&D projects to innovate & improve existing products & processes. -Equipment Maintenance: Oversee the proper maintenance & calibration of lab equipment. Coordinate repairs & equipment upgrades when necessary to optimize lab performance. -Process Improvement: Continuously evaluate lab processes and workflows to identify areas for improvement. -Training & Development: Provide training & ongoing support to lab staff to ensure their adherence to ISO 9001 processes and safety protocols. Foster a culture of learning & development to nurture talent within the team. -Regulatory Compliance: Stay up-to-date with industry regulations & best practices, ensuring that the lab operates in full compliance with all relevant safety, environmental, & quality standards. -Communication & Reporting: Maintain clear & effective communication channels with management, & external stakeholders Provide feedback to Top Management on customer and/or product issues and concerns -Basic experience with Syspro (BOMs, Stock code management, Inventory management) -Experience with XRF (WinFTM), FAAS, UVVIS, ICS, Titration

Quality Coordinator and Analyst

Biograde • Tiempo completo

Jan 2017 - Dec 2022 • 5 yrs 11 mos

My core responsibility were to help maintain the laboratory quality management system. This involved: -Monitoring quality control data by establishing, maintaining, and evaluating control charts (SPC Analysis) -Conducting internal audits according to ISO/IEC 17025 and SANAS requirements including witnessing and vertical assessments of accredited testing activities by IR, ICP-MS, ICP-OES, IC, GC-MS -Providing inputs to management reviews by evaluating trend analysis charts of TAT, CSS, NC&O, PT&ILC results -Coordinating PT&ILC participation and reporting outcome of schemes to top management My core responsibilities were to help analyse samples according to various Standard Test Methods (NIOSH, OSHA, EPA, etc). This involved: -Sample prep, calibration, analysis, and data calculations [ICS (Dionex/Chromeleon), HPLC (Shimadzu/LabSolutions), UVVIS (HACH) and various Gravimetric methods] -Assisted management with development of methods and installation of equipment -Helped with method validation and instrument maintenance