Qualification & Experience       Department : Central Laboratory             Qualification : Dip - DMLT, UG - B.Sc - Biochemistry, B.Sc - Microbiology, Others  Exeperience : Fresher : 0-1 yearExperience :1-3 years    

ResponsibilitiesDescription : Provides information for patient diagnosis and treatment by performing laboratory tests in Haematology, Biochemistry, Clinical Pathology, Micobiology, Serology, Immunology. Receiving, typing, testing, and recording Inventories.Qualification & Experience  Work Experience : 0-5 YearsQualification : MLT/DMLT/PGDMLT

Qualification & Experience           MBBS + MD Biochemistry     Experience as per NMC norms.            (2–3 yrs experience)                    

ResponsibilitiesRecording medical history and symptomsAdministering medication and treatmentCollaborating with teams for patient carePerforming point of care testsConducting nursing assessmentMonitoring patient’s healthProviding support and education to patient and familyMaintaining inventoryProviding bedside careOperating and care of medical equipmentAttending regular in-service educationQualification & Experience           Qualification: Graduate; 1st division in 10th, 12th and GNM Nursing/BSc Nursing/M.Sc NursingRelevant Experience:    3 months – 5 years of experience in field of Nursing assessing patient’s health problems, providing care to sick, disabled, recovering or injured patients, maintaining important medical records, implementing a nursing care plan and advising patients about maintaining health.Interpersonal relationship skillsListeningTeam buildingPerceptualCommunicationCoordination and cooperationInitiativeMoral support and physical approach to patientComputer literacyGNM Nursing/BSc Nursing/M.Sc Nursing     

ResponsibilitiesCommissioning & Qualification Lifecycle: Review and approve reports, protocols, and test documentation for commissioning and qualification of facilities, utilities, computerized systems, equipment, and laboratories in line with Lonza standards and regulatory expectations. GMP Design Review: Support the review of GMP design deliverables (flows, zoning, layouts) to ensure compliance. Deviation Management: Ensure discrepancies or deviations related to facilities and utilities are assessed, documented, traceable, and resolved. Periodic Requalification & Validation Maintenance: Review and approve periodic requalification documentation (e.g., freezers, autoclaves, HVAC, biosafety cabinets, cold rooms). Confirm validated state through validation maintenance reports. Review and approve decommissioning documentation as applicable. Quality & Risk Management: Review and support management of quality records (deviations, CAPA, change controls, investigations, product quality review). Maintain high standards of GMP compliance, documentation quality, and technical accuracy. Audit Readiness: Promote and maintain a state of audit readiness across qualification activities. Timely Delivery: Ensure assigned work is delivered within agreed timelines, proactively identifying and escalating risks or delays. Continuous Improvement: Contribute to process improvement initiatives and support implementation of new tools or approaches. Other Duties: Perform additional quality and compliance tasks as assigned. Education & Experience Qualification & ExperienceBachelor’s degree in Chemistry, Biochemistry, Pharmacy, or related scientific field. Minimum 5 years of relevant experience in regulated pharmaceutical industry (engineering, manufacturing, QA, QC). Experience in commissioning, qualification, and validation of manufacturing equipment, facilities, utilities, support systems, laboratory equipment, and computerized systems. Experience in process or cleaning validation beneficial. Proven experience in EMA/FDA regulated environments with strong knowledge of ICH, PIC/S, EU, and US regulatory requirements. Experience in chemical and biological GMP API manufacturing with ability to interpret and implement quality and regulatory requirements. Knowledge of CQV approaches and electronic validation tools (e.g., Kneat Gx).

Qualification & ExperienceMSc. in Analytical Chemistry / Organic Chemistry/ M. Pharm, having 10-13 years' experience in NMR or Ph.D. with 7-10 years of experience in NMR. Must have hands on experience in handling NMR instruments. Proficient in small molecule structure elucidation using NMR. Exposure to GMP/GLP environment and documentation procedures required. Expertise with Bruker NMR software- automation software & hardware including cryo-probes. Knowledge of solid state NMR and multinuclear NMR operations. A comprehensive understanding of the science involved in the development of synthetic organic molecules and analytical chemistry. Must be able to communicate effectively with both internal and external customers. Preferably familiar with electronic notebook documentation of experimental procedures. Must possess a strong work ethic and a solid record of problem solving and technical results.

ResponsibilitiesPrepare and analyze biological specimens for biochemical testing. Operate, calibrate, and maintain laboratory equipment such as spectrophotometers, analyzers, and centrifuges. Perform routine quality control procedures to ensure the accuracy and reliability of test results. Record and report results accurately in the laboratory information system. Assist in the troubleshooting of laboratory equipment and procedures.  Maintain a clean and organized laboratory environment and adhere to safety protocols. Collaborate with healthcare professionals to support patient care.Qualification & Experience Bachelor’s degree in Clinical Lab Science, Biochemistry, or a related field.3 to 6 years

Qualification & Experience                        Experience 2 to 5 years ExperienceQualifications M.Sc. Bio ChemistryKey Skillshigh analytical accuracy, proficiency in operating automated lab equipment, deep knowledge of clinical pathology, and strong communication skills          

ResponsibilitiesPerform method transfers/ validations / method verifications to the complex analytical techniques Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions. Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies. Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current. Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database. Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction. Qualification & ExperienceMaster’s degree in chemistry/ pharmacy with 5-7 years of experience in Analytical Method Transfer / Validation) Qualified in multiple analytical techniques (HPLC-with Empower, GC, IC, ICP-MS, Potentiometry, UV?Vis, FTIR, Karl Fischer, and pH meters) Demonstrated technical skills in method validation and testing Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations Conduct analytical method validation in accordance with ICH Q2 (R1/R2), USP, and EP standards, encompassing protocol preparation, execution, approval of validation summaries, and coordination with cross?functional teams. Conduct test method GAP assessments against USP, EP, BP, and JP requirements for New Product Introduction (NPI). Execute and document analytical method verification and method transfer activities. Demonstrate knowledge of ICH Q9 (Quality Risk Management) and apply risk?based principles for identifying, assessing, controlling, communicating, and reviewing quality risks throughout the product lifecycle. Perform identification, assay, purity, and related analytical tests using validated methods. Monitor critical process parameters (CPPs) and critical quality attributes (CQAs). Support process validation and troubleshooting activities; communicate analytical results promptly to Production and QA to ensure effective process control. Manage working standards in compliance with established procedures. Handle change control activities and ensure timely implementation and closure of related CAPA actions. Knowledge of Good Manufacturing Practices and its application standards, processes, and policies. Excellent organizational skills and strong ability to multi-task Strong written and verbal communication skills Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation

Responsibilities Work with product development, clinical, regulatory and any other cross-functional teams to support product innovation and development Provide inputs to formulation and analytical teams to identify product specific Bio-relevant/Bio-discriminatory media Identify in-vitro characterization tools and methodologies relevant to the in-vivo behavior of the formulations to select appropriate formulation strategies Evaluate data from biostudies to identify critical parameters (CMA, CFC, CPP) to enhance success in bioequivalence studies Perform mechanistic Modelling & Simulation to simulate the in vitro dissolution of active pharmaceutical ingredients (API) and formulation excipients under various experimental conditions and predict the in vivo pharmacokinetic profile Build and validate IVIVC/IVIVR for products when feasible Monitor and plan external development activities as required Search, compile and interpret scientific data, write reports, regulatory documents, manuscripts, and present work at internal and/or external meetingsQualification & ExpeirenceMasters in Pharmaceutical Science or a post-graduate degree in a related scientific discipline with a 7+ years’ relevant experience in the pharmaceutical industry.