Internal Job DescriptionEducation / ExperienceM.Sc. Analytical/Organic Chemistry/Inorganic ChemistryMin. 5 years’ Experience in a Quality Control/Analysis laboratory in a cGMP/ISO environment, with exposure to method development and validation activitiesTechnical skills &Competencies / LanguageTechnical competence.Leadership skills.Analytical ability.Planning ability.Communication skills.Problem solving.Team building.KEY ACCOUNTABILITIESAnalysis and approvalSampling, analysis and ascertaining quality of raw materials, packaging material, intermediates, In-process samples and API for Chemistry Ankleshwar.Testing of the method validation samples and process validation samples and cleaning validation.Perform analysis and documentation of API finished product stability study as per stability study protocol.Coordinating with Production, Stores and QA for Approval / Rejection of raw materials/finished product.Validation and verification of analytical procedures as per requirement.Reporting OOS / OOT results and deviations.Maintaining retained samples as per standard procedure.Assisting in investigation of customer complaint.Testing of new samples (Vendor approval)Training of subordinatesGive required suggestion for corrective actions and to plan effective preventive actions for the up gradation of the quality system.To ensure proper maintenance of the stability samples and their management.Disposal of waste according to the approved procedures.Continual reduction in the waste generation and effluent management.Co-ordination with microbiology lab (Pharmaceuticals) for microbial analysis of products and utilities.DocumentationGeneration, managing and archiving Documents including raw data, reports, COA etc as per requirements.Preparation and implementation of the SOPS in the laboratories system.Specification preparation and implementing for API raw material and API finished product according to requirement.Providing technical support in compiling Annual Product Review.Analytical method development when required.2.6.Executing on line documentationLaboratory ManagementQualification and Validation of instruments/equipmentsAppropriate training and guidance to the subordinates.Safety in the laboratory.Regular housekeeping and upkeep of the work area.Maintaining adequate inventory of chemicals and reference standards.Adapting relevant technologies and systems in Analytics.Laboratory equipment calibration and their maintenance.Developing training modules for improvement / training for HSE and QualitysystemsGenerate up gradation plans as need basis.Any other activity assigned by the In charge, AnalyticsRegulatory and other ComplianceCompliance to current GMP guidelines.Compliance to local and international HSE norms.Regulatory complianceISO 14000 related activities.Regular Pharmacopoeia and regulatory requirement review for compliance.To participate in any regulatory inspection that takes place at the site.Training of self and subordinates on quality and HSE systemsTeam memberMember of validation team.Member of Analytical transfer team.Participating in discussions and giving feedback to Manager, Analytics regarding on-going activities.Other projectsTrouble shooting activities.Participation in Industrial Excellence projects.Identifying and correcting unsafe conditions or behaviors and promptly reporting other potentially hazardous situationsPlant roundPlant round in absence of QA and during IInd and IIIrd shift.Online checking of critical process parameters during round.