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Flychem is looking for an experienced QA, QC, Analytical and Microbiology professional to take ownership of quality systems and laboratory operations covering raw materials, in-process materials and finished goods, including analytical testing, microbiology, method validation, stability, investigations and product release. Note: You can apply here on LinkedIN and share your CV to careers@flychem.com . Key Responsibilities - Lead QA/QC for raw materials, packaging materials, intermediates, in-process samples and finished goods. - Establish and maintain specifications, SOPs, STPs, sampling plans and release criteria. - Review and approve COAs, batch records, analytical reports and release documentation. - Manage testing by HPLC, GC, UV-Vis, FTIR, Karl Fischer, titration and other relevant techniques. - Develop, optimize, transfer and validate analytical methods. - Handle OOS, OOT, deviations, CAPA, change controls and non-conformances with root-cause investigation. - Plan and review stability studies, impurity profiles, retest periods and shelf-life data. - Ensure instrument qualification, calibration, preventive maintenance and data-integrity controls. - Manage reference standards, reagents, columns and laboratory documentation. - Coordinate with R&D; and manufacturing during development, scale-up and technology transfer. - Perform or supervise microbial limit testing, total aerobic microbial count, yeast & mold and specified pathogen testing. - Coordinate/review preservative efficacy / challenge testing, bioburden and microbiological method suitability/validation. - Oversee water microbiology, hygiene/environmental monitoring and microbiological investigations where applicable. - Qualify vendors and review incoming material quality performance. - Support customer/regulatory audits, technical queries and quality agreements. - Train and supervise QC analysts while maintaining GMP / GLP / ISO-aligned systems. Preferred Profile - M. Sc Chemistry / Analytical Chemistry / Microbiology / M. Pharm / B. Pharm or equivalent. - 5-10+ years of QA/QC, analytical laboratory or microbiology experience. - Solid hands-on understanding of HPLC/GC, analytical method development and validation. - Working knowledge of microbiological QC for cosmetics, pharmaceuticals, specialty chemicals or personal-care products. - Good understanding of OOS, CAPA, deviations, change control, stability and audit documentation. .