Medical Coding is the process of converting Medical Records into numeric or alpha numeric by using ICD 10-CM, CPT & HCPCS. Hr Priya 96004 50980 Designation - Medical Coder Trainee Profile UG / PG in Life Science, Paramedical, Bio Medical, Bio Tech Required Candidate profile Required Candidate profile Nursing Freshers Pharmacy Freshers Physiotherapy Dentist Life sciences Biotechnology Microbiology Biomedical Biochemistry Bioinformatics Botany Zoology DGNM B.Pharm M.Pharm Perks and benefits Incentive Up to 5k Healthcare Insurance cab & PF

Coordinates program related events such as workshops, symposia, national and international Scientific Events etc Designing scientific/technical sessions for the conference. Invite professors, Assistant, Associate from Universities Directors, Managers and Executive from Reputed companies throughout the world Be a main point of contact for Program chairs, session chairs, scientific committee and invited speakers Conference content/for all conference related communications, Content Marketing or Content Manager Forming organizing committee and scientific squad with top quality scientists on the particular research More intellectual in using scientific knowledge and footing on current scientific inventions Adopt/attain information on new finding in the all related research fields regularly To make event successful by providing fruitful information to the scientific community Plan and execute all web, SEO/SEM, marketing database, email, social media and display advertising campaigns Required Experience, Skills And Qualifications Required Skills Sets: A good academic background Excellent proficiency in English Language Good analytical skills and ability to work on different projects/different teams High level of attention to detail. Knowledge of office application like MS Excel, MS Word and PowerPoint will be an added advantage. Required Soft Skills: Highly committed and self-motivated Demonstrates willingness to take ownership for role responsibilities High regard for attention to detail and accuracy Ability to work to tight deadlines Proactive in identifying process improvements Demonstrates strong interpersonal and communication skills. Qualifications Required Bachelor/Master degree in Science/Pharma/Biotechnology B. Tech/B.E (All Branches) PG - M. Tech - Bio-Chemistry/Bio-Technology, Biomedical, M Pharmacy, Microbiology and all life sciences candidates Show more Show less

PhD Positions Open – Join Our Research Team I’m pleased to announce that three PhD positions are currently open in my lab. We are looking for passionate and committed researchers interested in contributing to high-impact work in the following areas: Gut microbiome and personalized therapeutics Microbial biofortification to address micronutrient deficiencies Antimicrobial resistance (AMR) and biofilm studies in the context of food safety Development of probiotic and prebiotic interventions as targeted therapeutics Our work sits at the intersection of microbiology, biotechnology, food and nutritional sciences, with a strong emphasis on translational research and societal relevance. We welcome candidates from backgrounds in microbiology, biotechnology, food science, or allied disciplines , who are motivated to work on real-world challenges using rigorous scientific approaches. These are full-time PhD positions with assured fellowship and access to excellent research facilities and collaborative opportunities. For more details visit www.niftem.ac.in . If this aligns with your research interests APPLY TODAY …. Last Date 05 th June 2025 Let’s build meaningful science together. Show more Show less

Company Name ID FRESH FOOD Job Title Quality Intern Job Location: Anekal, Karnataka Description About iD Fresh Food iD Fresh Food’s mission is to make healthy and nutritious homemade meals an easy task. Our range of fresh and authentic no-preservatives, no-added-chemicals range of ready-to-cook products help millions of households across India and GCC whip up tasty and wholesome meals. And we are expanding rapidly to the rest of the world too. About The Operational Model Much like our products, our business model is unique too. The distribution of our fresh products happens through direct shipping to retail stores. With zero finished good inventory, we do not depend on intermediary stockists or transitory warehouses. All this is made possible with the help of an in-house fleet of vehicles and distribution personnel. A fleet of 500 dedicated vehicles & crew reach 25,000 + retailers every day currently, and replenish 100,000+kg units of fresh produce. Job specifications Education: B-tech food technology / BSc or MSc food science / chemistry/ microbiology Experience: Fresher Communication: English & native regional language. Ability to communicate, in writing or verbally Industry: FMCG/ food production/ processing Roles & responsibilities Monitoring product conformance of RM/PM/FG. Monitoring cleaning of processing area and other plant areas Maintain GMP & 5S across the plant Implement quality & food safety system Monitor & verification of CCP/OPRP/PRP Monitor consumer complaints and taking corrective action Statistical process monitoring and improve quality in scientific way Chemical analysis of raw material, packaging material, finished goods & RO- water. Sensory analysis of raw material, finished goods, TPM products. Personal hygiene monitoring and shop floor training. Pest control monitoring and checking effectiveness of treatment. Updating QA files every day. Create & revision of SOP’s whenever required. Key skills Good level of knowledge in HACCP, food safety management system & quality management system. Customer complaint handling & root cause analysis & problem-solving tools. Basic knowledge about chemical analysis and microbiology Practical knowledge on food safety prerequisites such as GMP, cleaning & sanitation & pest control Strong organization skills and attention to detail. Highly disciplined, self-motivated, and delivery-focused individual, who can work independently. Demonstrated ability to synthesize information, prioritize business goals and drive results with a high sense of urgency and attention to detail. Apply Here https://www.idfreshfood.com/jobs/plant-quality-executive/ Show more Show less

Scientific Editor - Junior/Entry level in IP Content Editing Team - Delivering value-add scientific information for DWPI (Derwent World Patent Index) which is a proprietary database to easily search and identify Pharma. compounds covered in patents. Job Profile Summary : Extracting the novel scientific information from Pharma-related patents and value-add using DWPI codes in line with editorial policies for the DERWENT INNOVATION product. About You - experience, education, skills, and accomplishments Years of Service - Fresher or less than 2 years of relevant experience. Education - M.Sc Biotechnology, M.Sc Biochemistry, M.Sc Microbiology, M.Sc. Molecular Biology, B.Tech Biotechnology. Problem identification and solving skills, Good analytical skills. Outstanding communication skills (written and oral) with ability to communicate clearly, concisely, and objectively in both written and spoken English. Experience in analysing and interpreting complex datasets. Basic computer skills (Outlook, Word, Excel, PowerPoint). What will you be doing in this role? Responsible for indexing/coding biological compounds in patents. Extract information about Recombinant technology/ Genetic engineering/ Fermentation/ Enzyme nomenclature/ Identification of biological macromolecules (proteins, receptors, antibodies etc.) / Detection techniques of biological macromolecules/ Vaccine and its application/ Hybrid Plants from patents. Achieving target volume deliverables with high efficiency and quality. Play an active role in team and maintain awareness of current trends and new developments in Pharmabio areas. Responsible for tasks as requested by manager on a permanent or temporary basis. Prioritize and complete the tasks based on situation. Maintain a flexible and adaptable approach towards process change. Collaboratively work within and other teams to carry out the tasks and to be accountable for assigned responsibility. Trusted resource in achieving the customer delight.

Job Description Environmental monitoring and non-viable monitoring of classified areas. To perform GPT of prepared as well as ready to use media. To perform Sampling, Testing of Water samples and Cell bank testing. Preparation of Environmental monitoring trends. To perform Transaction in SAP/QAMS/EDMS/LIMS etc. as per authorization. Daily pH, Balance Calibration and Temperature, Humidity and D / P Recording. To perform Sterility test for RM, PM, and product. Preparation of Microbial Library for in house isolate identified from water and environmental monitoring samples. Sample receipt and management, Preparation of Glycerol stock. Operation of decontamination autoclave. Incubation of exposed Bl from autoclave validation and result recording. Preparation of Microbiology related SOPs / STPs /EOPs / Validation protocol and Report and Handling of Change Control, Deviation and CAPA Work Experience 1 to 3 years Education Masters in Microbiology or Biotechnology Competencies

Job Description Daily pH, Balance Calibration and Temperature Recording. Cleaning and disinfection of the controlled areas To perform Compressed air sampling and analysis. Sample Receipt as per respective protocol/specifications. To perform Environmental monitoring and EM Trend Preparation. Sub culturing, serial dilution of standard cultures and CPT. Preparation of Microbial Library for in house isolate identified from water and environmental monitoring samples. Incubation of exposed Bl in autoclave validation and its result reporting. To perform Population Determination of Biological Indicators. Operation of decontamination autoclave. To perform Transaction in SAP and QAMS as per authorization. To monitor temperature data of incubators in Lisa line. To ensure online documentation as per GMP requirement. To perform activities as per authorities provided for LIMS. To Perform Bioburden, BET test for water, RM and Product and Sterility testing. To perform Water sampling, Water testing and Water continuation. Preparation of Microbiology related SOPs / STPs. Any responsibility advised by the superior from time to time. Work Experience 1 to 4 year experience Education Post Graduation Masters in Microbiology or Biotechnology Competencies

Process: *Retrieve the correct medical record of a patient, review & validate completeness of documentation along with signatures, orders for diagnostic tests etc. * Review and validate and/or modify, providers, Dates of service, CPT codes, Diagnoses and modifiers by following general coding guidelines, payer specifications and client specifications if any. *Adhere to the standard operating procedures and instructions related to the process in coding. * Communicate if there are documentation deficiencies or any other issues which prevent compliant coding. * Be focused on self learning and update his/herself with the latest updates of the coding industry. * Keep their coding credentials active by submitting their CEUs and renewing their credentials. * Minimum graduation in any of the above mentioned disciplines Life sciences graduates--B.Sc (Biotechnology, chemistry, zoology, Botany, Microbiology, Genetics, etc) Mandatory active coding certification such as CPC, COC, CCS-P.

Job Title: Senior Specialist, Microbiology Location: Vadodara Job Model: Office Role Purpose of the position: Purpose of this position to maintain and continually improve the quality of products, processes & quality systems to provide right quality and services to the customers. Supports the implementation and execution of the quality, food safety, cleaning, and sanitation management systems within DSM-F HNC Premix Ensure the smooth operation of the Microbiology instruments for daily sample analysis Responsible for the calibration and preventive maintenance of the microbiology instrument and equipment as well as coordinating with the supplier/vendor of the equipment in case of breakdown and Preventive maintenance. Maintains the master equipment list and ensures that the performance verification methodologies conform to some recognized standards and the equipment is operating under validated specifications. Ensure that the units are operating according to specifications, Ensure that appropriate inventory of consumables are maintained for lab operations. Responsible for test method development and transfer, qualification of test methods and new laboratory instruments according to Pharmacopeia/In house/ ISO methods and Customer requirement any failure investigation of test method/procedure of Instrument. Assists the QA/QC Manager in maintaining the QMS microbiology and FSSC 22000 system implemented in the plant. This includes reviewing and improving on the existing process, procedures and instructions. Ensure that lab operations are carried out as per good laboratory practice (GLP). Key responsibilities: Ensure the smooth running of the Microbiology laboratory RM, PM and FG analysis are done as per their specification. Culture Maintenance. Environmental Monitoring. In-charge of the calibration and Preventive Maintenance of instruments and equipment to ensure good quality of Microbiology results. Preparation and updating SOP regarding microbiology standard methods. Source and recommend new test instrument when required and carry out qualification (IQ, OQ & PQ) of the instrument with the vendor so as to put it to use for routine testing in shortest time possible. Maintain technical data, generate reports and findings. Write relevant instrumental or procedural SOPs for the work operations. Assist the QA Manager to review and improve Microbiology procedures and instructions related to the ISO QMS and FSSC 22000 standards/LOP/SOP. Calibration and validation of Microbiology equipment. Risk assessment Microbiology Ensure that plant EMP programme is thoroughly implemented. Ensure Plant Environmental contamination incidents are investigated thoroughly and support to improve overall hygiene standards. Ensure that DSM cleaning and sanitation standards are adhered across the site. Support region for Hygiene related investigations and serve as a key resource. Conduct shop floor Gemba walks and suggest areas for improvement for hygiene/ sanitation. Actively involve in cleaning validations and verifications. Look for opportunities of cost savings in sanitation practices. Responsible for actively participating in Change management (MOC) risk assessment related to Hygiene/ sanitation. Conduct regular trainings to shop floor team on cleaning and sanitation standards. Escalate Food safety risk indicators if any from time to time to the senior management and prevent food safety risks. Keep himself/herself abreast of latest hygiene/sanitation standards and implement best in class standards. Conducts staff training of site cleaning and sanitization procedures. Oversees & monitors housekeeping and cleaning programs. Performs daily audits of manufacturing and production to identify micro risk areas, clean design defects, and proper adherence and execution of C&S procedures. Oversees teardown and re-assembly process from a hygienic perspective. Participates in company continuous improvement initiatives by seeking out improved ways to clean and sanitize more efficiently & effectively. Coordinates with other operational units to maintain compliance and perform. Communicates with all sites in the region and globally to ensure consistency and sharing of best practices.

We( Sanzyme biologics, karakapatla unit )need executives, 2 in number with 2-3 years of experience in downstream operations for our recombinant proteins at PU 3. Qualification: B.Tech / M. Sc in Biotech / Biochemistry / Microbiology with 2-3 years of experience in downstream operations for recombinant proteins. Job Desciption: Handling TFF for micro and ultra filtration systems Handlng continuous centrifuge of varied capacities Handling Chromatography systems with audit trailing Column Packing and Un packing for the high scale BPG columns Buffer preparations as needed Sterilization of process materials Working in shifts is mandatory Aware of clean room procedures Hands on with the integrity testing Thorough with the documentation practices Aware of SOPs and the heirarchy... Interested can share their cv to my pw.. tq Show more Show less

Aster Medcity is looking for Technician.Laboratory to join our dynamic team and embark on a rewarding career journey. Conducting electrocardiogram (EKG), phonocardiogram, echocardiogram, and stress tests by using electronic equipment. Ensuring cardiology patients are comfortable by answering any questions they have about the tests. Recording the results of cardiological tests and consulting with the physician on duty to schedule any follow-up tests. Assisting physicians during non-evasive cardiological procedures by monitoring the patients' heart rates and alerting the physicians to any readings outside normal ranges. Maintaining cardiological equipment and supplies with daily cleanings and adjustments. Recording supply inventory levels and restocking the supply storeroom accordingly. Troubleshooting problems with cardiological equipment and reporting any malfunctions to superiors. Staying up-to-date with cardiological developments by attending conferences and participating in research projects

Research & Development The Global Compliance Quality Team manages the quality performance of Reckitt, also providing oversight of the Quality Management System (QMS) and Quality compliance programmes. The team provide quality metrics KPI and insights for the end-to-end supply model (Factories, EMOs and Commercial Teams), utilising the metrics data to drive continuous quality improvement and compliance efficiency, also using coaching and influencing skills to ensure quality issues are effectively addressed and preventative actions are suitably embedded. In addition, the team provides support and leadership of key strategic compliance continuous quality improvement projects (QIPs). The team supports the Reckitt group to ensure Factories, Commercial Units and External Manufacturing Quality groups remain compliant with regulatory requirements for the countries of manufacture and sale, via compliance with Reckitt QMS and internal standards. They will partner factories and commercial units in the preparation for, hosting of and completion of responses to international GMP audits, also use risk-based methods to generate and manage the Reckitt Cross audit plans. To achieve this role holder will (both directly and indirectly through influencing others): To support in driving the compliance agenda across all sites, EMO, DC and Commercial Units; partnering with Region and Supply Leads. To support the network of Compliance Teams in gathering, report and analysing Factory, Commercial units, and EMO group Key Quality Metrics. To lead collation of weekly, monthly, and quarterly quality reporting, ensuring continuous improvement of content and format, based on feedback and business requirements. To work closely with the quality leads to track progress of the actions from GRIs and significant quality issues to ensure actions are closed out as committed. To support Hygienic Design network with KPIs, and support with implementation of Global hygiene design initiatives. To support, deploy and monitor the global initiatives like 6-to-fix priority projects. To lead selected quality improvement projects as identified by the Global Reckitt Supply / Quality teams. To prepare monthly performance review for Reckitt Supply and Quality Leadership Teams, including KPIs and GRI trends, and progress of key initiatives. To collate and monitor compliance data across Reckitt, analysing data to propose Global action plans. Support and deputise for the Global Quality Compliance and Performance Senior Manager. About the role Scope: Reporting to the Global Quality Compliance and Performance Manager, the primary scope of the role is: Operating as part of the Reckitt Global Quality Compliance & Performance team. Support the Reckitt factories, Commercial Units and External Manufacturing Quality groups with metrics collation and facilitate the cascade of the Global metrics, for input into the Total Reckitt. Lead, support and coach factories, commercial units and EMO groups with Compliance and Quality Improvement activities. Develop and deliver training across Global Reckitt, along with routine coaching of best practices in areas such as root cause problem solving, CAPA generation and quality risk management. Supporting the factories, Commercial Units and EMO Quality groups to be at a constant state of audit readiness, ensuring procedures are kept up to date with current business and regulatory expectation, and in line with Global Reckitt QMS. Assists with the collation of the necessary Reckitt post market surveillance activities in support of the Global Medical devices ISO certification. Accountability: On time delivery of monthly collation of Global KPIs on behalf of Global Reckitt Director, including input into the Cross-business metrics Core Reckitt, Essential Home and MJN. Analysis of KPI data to provide recommendation to the Reckitt on key priorities for resolution, or potential emerging compliance risks. Generation of relevant weekly, monthly, and quarterly quality reporting; ensuring continuous improvement of content, based on feedback and business requirements. Lead and support Quality improvement projects for the Reckitt. Lead and guide factories with the completion of the Self-Assessment Standards and implement processes and targets which support the achievement of quality standards; accurately presenting findings and leading the thinking to ensure appropriate actions are driven at a site level. Makes recommendations and leads actions to improve process, procedures and systems with respect to the Global Reckitt QMS, and in support of Factory QMS; ensuring where possible that key learnings and requirements are captured Globally. Develops and maintains personal expertise in key areas such as relevant legislation and GMP guidelines. This will be achieved through a systematic and recorded CPD process (continuous professional development). Your responsibilities Key Challenges: Reporting KPIs within timeframes given and chasing up any discrepancies with sites, commercial units and EMO groups to ensure all metrics are correctly reported. Support and implement the vision to automate Compliance data and improve overall process efficiency. Effectively prioritise workload based on risk and business benefit. Ability for International travel and flexibility with working hours due to the time zones of the associated Heath factories. Audit readiness - Minimise regulatory adverse comment with regards the Reckitt Factories. Supporting the Global Quality Compliance and Performance Senior Manager in influencing the Factories and External manufacture Quality Management groups to maintain compliance with regulations and Reckitt standards whilst communicating key learnings within the group to drive improvement. Leading or supporting various quality improvement projects within the Reckitt Supply group. Coach best practices across the Reckitt supply group. Technical / professional qualifications required: Educated to degree level Good understanding of Reckitt factory operations, QC testing operations and quality management systems. Broad understanding of Reckitt manufacturing operations business. Skilled in collation and reporting of performance metrics, including analysis of data and storytelling Knowledge of the legal requirements, rules and guidance covering the manufacture of pharmaceutical products, medical devices, cosmetics, food and general product in Europe (preferred). Experience in a manufacturing environment. The experience were looking for At least 5 years of experience working in a quality and or regulatory compliance function in a Reckitt, Pharmaceutical, or Medical Device related FMCG industry. Experience in developing and maintaining a robust QMS. Good understanding of typical regulatory requirements relevant to a regulated product e.g. EU GMP, WHO, PIC/S, CFR 21 Part 111/ 210/ 211/ 820, ISO stds 13485 + 22716, etc.. Plus others. Good working knowledge of Industrial Pharmaceutical Microbiology and Hygienic Design requirements Strong communication skills Well-developed influencing skills. Diplomatic and tactful in challenging situations. Highly motivated and able to self-manage time and workload. Organised and able to deliver concise written or oral summaries to senior management. Capable of linking data sources together and translating to drive business improvement. Including PowerBI proficiency in Excel & PowerBI and other software used to analyse data. High attention to detail. Problem-solving aptitude and experience in use of root cause problem solving tools.

Job Title: Senior Specialist, Microbiology Location: Vadodara Job Model: Office Role Purpose of the position: Purpose of this position to maintain and continually improve the quality of products, processes & quality systems to provide right quality and services to the customers. Supports the implementation and execution of the quality, food safety, cleaning, and sanitation management systems within DSM-F HNC Premix Ensure the smooth operation of the Microbiology instruments for daily sample analysis Responsible for the calibration and preventive maintenance of the microbiology instrument and equipment as well as coordinating with the supplier/vendor of the equipment in case of breakdown and Preventive maintenance. Maintains the master equipment list and ensures that the performance verification methodologies conform to some recognized standards and the equipment is operating under validated specifications. Ensure that the units are operating according to specifications, Ensure that appropriate inventory of consumables are maintained for lab operations. Responsible for test method development and transfer, qualification of test methods and new laboratory instruments according to Pharmacopeia/In house/ ISO methods and Customer requirement any failure investigation of test method/procedure of Instrument. Assists the QA/QC Manager in maintaining the QMS microbiology and FSSC 22000 system implemented in the plant. This includes reviewing and improving on the existing process, procedures and instructions. Ensure that lab operations are carried out as per good laboratory practice (GLP). Key responsibilities: Ensure the smooth running of the Microbiology laboratory RM, PM and FG analysis are done as per their specification. Culture Maintenance. Environmental Monitoring. In-charge of the calibration and Preventive Maintenance of instruments and equipment to ensure good quality of Microbiology results. Preparation and updating SOP regarding microbiology standard methods. Source and recommend new test instrument when required and carry out qualification (IQ, OQ & PQ) of the instrument with the vendor so as to put it to use for routine testing in shortest time possible. Maintain technical data, generate reports and findings. Write relevant instrumental or procedural SOPs for the work operations. Assist the QA Manager to review and improve Microbiology procedures and instructions related to the ISO QMS and FSSC 22000 standards/LOP/SOP. Calibration and validation of Microbiology equipment. Risk assessment Microbiology Ensure that plant EMP programme is thoroughly implemented. Ensure Plant Environmental contamination incidents are investigated thoroughly and support to improve overall hygiene standards. Ensure that DSM cleaning and sanitation standards are adhered across the site. Support region for Hygiene related investigations and serve as a key resource. Conduct shop floor Gemba walks and suggest areas for improvement for hygiene/ sanitation. Actively involve in cleaning validations and verifications. Look for opportunities of cost savings in sanitation practices. Responsible for actively participating in Change management (MOC) risk assessment related to Hygiene/ sanitation. Conduct regular trainings to shop floor team on cleaning and sanitation standards. Escalate Food safety risk indicators if any from time to time to the senior management and prevent food safety risks. Keep himself/herself abreast of latest hygiene/sanitation standards and implement best in class standards. Conducts staff training of site cleaning and sanitization procedures. Oversees & monitors housekeeping and cleaning programs. Performs daily audits of manufacturing and production to identify micro risk areas, clean design defects, and proper adherence and execution of C&S procedures. Oversees teardown and re-assembly process from a hygienic perspective. Participates in company continuous improvement initiatives by seeking out improved ways to clean and sanitize more efficiently & effectively. Coordinates with other operational units to maintain compliance and perform. Communicates with all sites in the region and globally to ensure consistency and sharing of best practices.

Core job responsibilities: Provide superior customer service, through applying effective communication skills in order to build loyalty while proactively managing and resolving high-stress situations Delight our customers by providing support including training, TOR Troubleshooting, and following-up, and closing calls as per Abbott Diagnostics quality system including immunology and bio-chemistry system. Partner cross-functionally and internally while maintaining positive relationships and ensure issues are resolved efficiently and satisfactorily while exceeding customer needs Successfully achieve the established business metrics including service sales, cost of service and key performance indicators for assigned customers/accounts Champion utilization of remote support tools to proactively improve instrument up time Proactively improve expertise through continuous learning and certifications Supporting Commercial Team in Technical queries customer s discussion and in Conferences and Technical seminars. Supervisory/Management Responsibilities Direct Reports No Indirect Reports NO Comments: Must be able to influence other areas to achieve business goals Education and experience: Master s degree or equivalent in Science(Microbiology / Biochemistry) relevant experience required. Practical experience of interfacing with customers preferred. Additional Skills: Trouble shooting/problem solving, ability to succeed in team situations and excel independently, computer skills (Word, Excel, Power Point, Internet, Remote Computing i.e VPN, remote troubleshooting etc.), effective communication skills and strongly demonstrated interpersonal skills. Language: Basic English skills are preferred (written and oral). Proficiency in local language required. JOB FAMILY: Support Services DIVISION: CRLB Core Lab LOCATION: India > Bangalore : Jigani Link Road t

Job Title : Microbiologist Entity : Bureau Veritas India Pvt Ltd, INDIA (BVIL) Location : Chennai Reports to (job) : Manager/ Assistant Manager – Microbiology Ø Purpose of Position Responsible for carrying out media preparation for Mmicrobiological analysis and responsible for disposal of used media and contaminated samples The position performs in line with the Bureau Veritas Lab testing activities including the BV Code of Ethics and the BV Group policy. Ø Major Responsibilities Report to the Manager – section In-Charge Responsible for performing analysis of Food & Agricultural products, Sea foods, Environment, textile samples as per IS/ISO/BAM/APHA methods. Responsible for handling of equipment related to Microbiological lab.. Responsible to carryout Standard culture activation, verification, maintenance and disposal Responsible for sample storage and waste disposal. Responsible for carrying out analysis of Pharmaceutical samples as per API & USP. Responsible for daily verification and intermediate check of Equipment’s.. Responsible for writing raw data and maintenance of documents and records pertaining to the activities as per ISO 17025-2017 Other tasks as required. Ø Roles & Responsibilities for HSE Must comply the BV Cardinal Safety Rules in all situations. To comply company HSE requirements e.g. policies, Procedures, guidelines etc. and local legal requirements on HSE as applicable To take care of own health and safety as well as colleagues and others. Immediate reporting of any shortcomings on HSE i.e. any incident, unsafe work practices / conditions to his/her immediate Line Managers. Ø Criteria for Performance Evaluation (KPIs) Reporting results as per TAT Technical competency and performance in the Audit. Achievement of Z score in PT ILC. Addition of new techniques and updating latest skills Show more Show less

Overview: TekWissen is a global workforce management provider throughout India and many other countries in the world. Position: Scientist - Strain Engineering Location: Gurugram Work Type: Onsite Job Type: Full time Job Description: We are currently looking for an experienced Scientist to work in the field of synthetic biology and Microbial Genetics. Job responsibilities includes: Work with laboratory strains of Escherichia coli, fungi, yeast etc using aseptic technique for culturing, maintenance, and transformation. Perform advanced molecular biology techniques like recombinant cloning, assembling, genome editing and recombinant knockouts. Perform genome editing of micro-organisms for improved phenotype and heterologous production of recombinant molecules. Carry out fermentation studies for recombinant strains for yields and scale up studies. Design, implement, and characterize novel gene constructs. Metabolic engineering of recombinant strains and analyzing flux. Prepare and execute established methods and SOPs. Deliver high-quality results in a timely manner and communicate the same with stakeholders. Drive process improvements Maintain all equipment, data and records as per specifications. Educational and Essential Qualifications: M.Sc./Ph.D. in molecular biology, microbiology, biochemistry, biotechnology, synthetic biology or related field. 2+ years of postdoctoral experience in academic, pharmaceutical, or biotechnology industry settings working different recombinant platforms for production of novel molecules like flavours and fragrances. Experience in metabolic pathways engineering of Yeast and bacterial systems using advanced molecular biology tools. Experienced in working with metabolic pathways prediction tools. A strong grasp of fundamental molecular biology techniques is essential. Exposure to gene circuit design, cell engineering, strain development, is highly desirable. Demonstrated ability to work with highly skilled teams in a fast-paced, entrepreneurial and technical environment. Excellent communication and presentation skills, capable of conveying technical information in a clear and thorough manner. Comfortable delivering against challenging commitments. Confident, execution focused, team oriented, with an ability to thrive in an entrepreneurial environment. A desire to work in the impact space, with a passion to make the world a "better" place. TekWissen® Group is an equal opportunity employer supporting workforce diversity. Show more Show less

Inspection & Certification Division: FARE Labs Pvt Ltd, Gurgaon Job Title: Empanelment of Auditors- Dairy Sector Job Description: Educational Qualifications: Candidates must possess a Master’s degree in one of the following disciplines from a recognized university: Food Technology, Dairy Technology, Fisheries, Oil Technology, Biotechnology, Agriculture, Veterinary Sciences, Biochemistry, Microbiology, Chemistry. Essential Requirements: Additionally, candidates must have successfully completed an accredited Lead Auditor Course in Food Safety Management Systems (ISO 22000). Professional Experience: Applicants must have a minimum of 4 years of relevant experience in the following areas: Conducting audits and inspections in alignment with international standards, including ISO/IEC 17020, ISO/IEC 17021-1, and other applicable quality or regulatory frameworks. Demonstrating comprehensive knowledge of dairy sector operations, processes, and safety standards. Implementing or evaluating Hazard Analysis and Critical Control Points (HACCP) systems within dairy industry settings. A minimum of 10 man-days of audit experience in dairy industries conducted under ISO 22000 standards. Knowledge & Skills: 1. Strong communication and interpersonal skills. 2. Proven ability to prepare and deliver clear, well-structured, and professional audit reports and documentation. Salary: As per industry norms. Kindly share your CV at: hr@farelabs.com Show more Show less

Job Description Responsible to participate in perform qualification activities of manufacturing and Microbiology area Responsible for Compressed air /nitrogen gas monitoring and Personnel monitoring. Planning and execution for environmental monitoring of manufacturing and microbiology lab clean room area as per the defined schedule Planning of compressed air /nitrogen gas monitoring and personnel monitoring. To perform calibration/qualification of instruments/equipment as per predefine schedule. Responsible to participate in media fill simulation study. Handle sterility testing, Handling of microbial identification, Handling of bacterial endotoxin test Qualifications Qualification: B.Sc./M.Sc./B. Pharm Show more Show less

To ensure microbiological quality assurance and compliance of pharmaceutical products by overseeing and validating microbiology lab activities, documentation, and adherence to cGMP, regulatory guidelines, and company SOPs. Key Responsibilities Microbiological Testing & Daily Lab Operations Sampling and testing of: Raw materials (API & excipients) In-process materials Finished products Stability samples Routine testing: Total microbial count (bacteria/fungi) Pathogen detection (E. coli, Salmonella, P. aeruginosa, S. aureus) Water testing: Purified Water (PW), Water for Injection (WFI), and Potable Water Swab testing for equipment and personnel hygiene Environmental monitoring of manufacturing areas: Air sampling (viable and non-viable particles) Settle plate analysis Contact plate and swab testing on surfaces Compressed air and gas monitoring Documentation & Compliance (Lab-QA Functions) Preparation and review of: Standard Operating Procedures (SOPs) Specifications and test methods Analytical and microbiological reports Ensuring GDP (Good Documentation Practice) and ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate + Complete, Consistent, Enduring, Available) Routine checks and approval of logbooks, analytical data, and lab records Involvement in data integrity audits and ensuring lab systems are 21 CFR Part 11 compliant (if applicable) Instrument Handling, Calibration & Qualification Operation, maintenance, and calibration of instruments like: Incubators, BOD incubators Laminar air flow units (LAF) Particle counters (non-viable monitoring) Autoclaves and hot air ovens pH meters, conductivity meters Ensuring timely calibration and preventive maintenance as per schedule Preparation of equipment qualification protocols and reports (IQ/OQ/PQ) Validations & Support to Production Participation in: Cleanroom validation (viable & non-viable monitoring) Disinfectant efficacy studies Media fill validation for process simulation (if sterile environment is involved) HVAC validation support Support in vendor qualification for microbiological consumables (media, reagents, disinfectants) Deviation, OOS, OOT & CAPA Handling Root cause analysis for any deviations, out-of-specification (OOS), or out-of-trend (OOT) microbiological results Initiation and follow-up of corrective and preventive actions (CAPA) Support in market complaint investigation related to microbiological quality Audits, Regulatory Compliance & Training Prepare for: Internal GMP audits External regulatory inspections (USFDA, MHRA, ANVISA, WHO, etc.) Customer audits Documentation support for Site Master File (SMF), Validation Master Plan (VMP), and Product Dossiers Educational Qualification B.Sc. in Microbiology / Biotechnology M.Sc. in Microbiology / Biotechnology Show more Show less

JOB TITLE: Research Executive FUNCTION: Science & Technology REPORTS TO: Senior Research Scientist SCOPE: Personal Care, Science and Technology, Biological Science WORK LOCATION: Unilever R&D Bangalore With 3. 4 billion people in over 190 countries using our products every day, Unilever is a business that makes a real impact on the world. Work on brands that are loved and improve the lives of our consumers and the communities around us. We are driven by our purpose: to make sustainable living commonplace, and it is our belief that doing business the right way drives superior performance. At the heart of what we do is our people - we believe that when our people work with purpose, we will create a better business and a better world. At Unilever, your career will be a unique journey, grounded in our inclusive, collaborative, and flexible working environment. We don t believe in the one size fits all approach and instead we will equip you with the tools you need to shape your own future. BUSINESS CONTEXT AND MAIN PURPOSE OF THE JOB: Personal care (PC) is focused on Unmissable Brand Superiority and Making Market with Multi-Year Innovation Platforms and Excellence with Incremental turnover (iTO). Science & Technology (S&T) team is focused on big bets platforms such as Biotechnology, Microbiome, Advanced Materials, using E2E Digital to excel with savings and growth. The role of the Science and Technology (PC Biosciences Science and Technology) is to deliver breakthrough Differentiated & Superior Technologies to meet above PC goals, in key markets and with power brands. The Personal Care Bioscience team is focused on generating insights and delivering new technologies for various brands within the Personal Care Category (PC). This involves developing scientific understanding and capabilities in Host-Microbiome interaction. A key aspect of the program is to build the capability to understand how actives and formulations interact with both the host and microbiome, including the host response to deposited actives and their synergy with metabolites from bacteria and human cells. This work is essential for evaluating technologies, understanding the mechanisms of bacterial and host interplay, and developing new microbiome management technologies for PC categories. MAIN ACCOUNTABILITIES: Use existing methodologies for in vitro and in vivo evaluation of technologies that interact with human skin. Screen and identify novel molecules that trigger and/or synergize with skin microbiome for host benefit. Execute experimental protocols and methodologies to identify and measure perturbation of skin benefit markers. Develop capability to analyze and interpret microbiomics data generated from internal clinical study. Keep up to date on scientific literature. Interpret data and communicate scientific results through data tools, electronic lab notebooks, technical reports and presentations. Effective team working with other members of the Biological Science team located in Bangalore and other Unilever R&D sites. Key R&D Interfaces: Global benefit platform leaders Patent attorney Academic, Institutional & external partners Key Skills: M. Sc. in Life Sciences or Microbiology or Biochemistry or Cell Biology or Biotechnology. 1 to 3-year experience in Cell Biology/Animal tissue culture and Microbiology gained either in an industrial or academic research, post MSc degree. Experience in experimental design, data analysis, data validation and documentation. Basic appreciation of statistics and data analysis tools. A team player and has good communication and presentation skills. Interested to develop knowledge and understanding of current and emerging techniques that could be used to enhance project deliveries. Well organized, self-motivated, enthusiastic, and confident. Our commitment to Equality, Diversity & Inclusion Unilever embraces diversity and encourages applicants from all walks of life! This means giving full and fair consideration to all applicants and continuing development of all employees regardless of age, disability, gender reassignment, race, religion or belief, sex, sexual orientation, marriage and civil partnership, and pregnancy and maternity.

Key Responsibilities: Write and review high-quality academic content across Life Sciences subjects including Biotechnology, Biochemistry, Microbiology, and Molecular Biology. Prepare clear, structured explanations, learning materials, and concept-based questions for higher education learners. Ensure scientific accuracy, proper referencing, and adherence to academic writing standards. Collaborate with editors and SMEs to revise and finalize content as per project guidelines. Meet content production deadlines while maintaining quality benchmarks. Key Requirements: Academic background in Life Sciences (Biotech, Microbiology, Zoology, Botany, etc.) Strong English writing skills Knowledge of scientific terminologies and ability to simplify content Prior experience in educational content writing is desirable. Subject Knowledge in Life Sciences or Related Disciplines.

To prepare, review and approve Quality Control-Microbiology Documents-Study Protocol, General Test Procedure, Specifications, Qualification Protocols. To perform and review daily Verification, Calibration of Quality Control-Microbiology instruments. To prepare and review the Trend data of Water and Environment Monitoring. To perform sampling, analysis & observation of water and recording relevant data. To perform and review Microbiological Limit Test/Method suitability testing of raw material, in-process and finished products. Preparation and review of culture media and performance of growth promotion test of media. To review the Microbiology reports and documentation. Preferred candidate profile 5 - 6 yrs of experience in Microbiology M Sc in Microbiology or Biotechnology Interested candidates may share profile at hr.plant@zuventus.com

Role & responsibilities : Water sampling and testing, Manufacturing and Sterility area Media Preparation Environmental Monitoring Swab Analysis Microbial Limit Test Autoclave handing Analytical Method Validation for Raw Materials Preferred candidate profile : 3 - 5 yrs of experience in OSD. M Sc. - Microbiology Interested candidate may share updated profile at hr.plant@zuventus.com

Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait . We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. Job Description We are looking for an individual to work with Site Investigations team member (Microbiology) ensuring the conducting the effective investigations and root cause analysis and drive them towards closures in timely manner with adequacy. Key Responsibilities: Site Investigation Team member (Microbiology) is responsible for performing root cause analysis for microbiology-related deviations, Out of Specification (OOS), and Out of Trend (OOT) results, including Bioburden, Sterility, and Bacterial Endotoxins Test (BET). This role involves collaborating with cross-functional teams to ensure timely and adequate closure of investigations, conducting trend analysis, ensuring appropriate Corrective and Preventive Actions (CAPA), and periodically reviewing recurring deviations to present findings to management. Root Cause Analysis (RCA) Identify and define microbiology-related deviations, OOS, and OOT events. Gather and analyze relevant data to identify potential root causes. Utilize tools such as fishbone diagrams, 5 Whys, and Pareto analysis to determine root causes. Verify root causes through additional testing or investigation. Collaboration with Cross-Functional Teams Form and lead cross-functional teams including members from Quality Control, Quality Assurance, Production, and other relevant departments. Schedule and conduct regular meetings to discuss progress and findings. Maintain detailed records of all discussions and decisions. Trend Analysis Collect and analyze data on deviations, OOS, and OOT over specified periods. Use statistical tools to identify patterns or recurring issues. Prepare and present trend analysis reports to management and relevant stakeholders. Corrective and Preventive Actions (CAPA) Develop appropriate CAPA based on root cause analysis. Ensure timely implementation of CAPA. Monitor and review the effectiveness of CAPA and make necessary adjustments. Periodic Review and Management Reporting Periodically review recurring deviations and their root causes. Prepare detailed reports for management, highlighting recurring issues and the effectiveness of CAPA. Present findings to management and discuss potential improvements. Qualifications Educational qualification: A Post-Graduation in Sciences (Bioprocess, Biotechnology, Life sciences), Pharmaceuticals. Minimum work experience : 10 to 12 years of experience in Microbiology/ Sterility Assurance/Drug Product in pharmaceutical and biopharmaceutical industries Skills & attributes: Technical Skills Strong comprehension of process and analytical investigations and Understanding of counter functions within the organization and their relationship to quality processes. Familiarity with quality assurance processes and investigation and root cause methodologies. Deep understanding of cGMP (Current GMP) across various phases of the product life cycle (Process and Analytical). Knowledge of quality management principles and practices, including quality control and quality assurance. Broad understanding of the development and production processes, and equipment and utilities required within the pharmaceutical manufacturing, sterility assurance concepts and quality control. In-depth knowledge of both the products and the processes involved in the Bio Pharma and Pharma sectors. Proficient auditing skills, and an understanding of national and international regulatory guidelines relevant to the pharmaceutical industry. Behavioral Skills Strong communication and influencing skills. Commitment to continuous learning and coaching. Displays risk-based decision-making skills. Excels in building and leveraging relationships, with a focus on strong team-building. Commitment to innovation and effective problem-solving. Prioritizes integrity in all aspects of work. Additional Information About the Department Biologics Currently operates in the Global Biosimilars business - a segment that is poised for attractive and sustained growth over the next 10–15-year time horizon. With a robust portfolio of biosimilar products across key therapeutic areas, covering ~US$80+ Bn in innovator sales – future business pipeline covers a variety of product classes and therapy areas, and new modalities. Fully integrated organization with over two decades of experience in developing, manufacturing and commercializing multiple biosimilar products. With a Product Development engine that has end-to-end capabilities – in-house clone development, upstream and downstream process development, bioanalytical development and proprietary formulation. Supported by a Clinical and Regulatory team with experience in executing complex biosimilar programs with innovative global trial designs. We have a proven experience in commercial-scale manufacturing across a variety of technology platforms with global quality standards and a highly competitive cost structure Rich experience of commercializing high-quality biosimilars in multiple markets with over 900,000 patients having benefited from our products till date. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/ Show more Show less

About the Role: Daksha Organics is hiring a Microbiologist to assist in ensuring the microbial safety and shelf-life stability of skincare formulations such as sunscreen and gels. Key Responsibilities: Conduct microbial limit testing (TVC, yeast, mold, pathogens) of skincare products. Perform environmental monitoring of lab and equipment. Support preservative efficacy testing (PET/challenge tests). Document and analyze results with clarity. Work alongside the formulation chemist during trial batch validations. Requirements: B.Sc. / M.Sc. in Microbiology or related discipline. 1–2 years of experience in microbiological testing of cosmetics/pharmaceuticals preferred. Knowledge of testing standards (BIS/IS, ISO, etc.) for skincare products. Ability to maintain aseptic technique and lab protocols. Accuracy in sample handling and reporting. Job Type: Full-time Pay: ₹20,000.00 - ₹25,000.00 per month Work Location: In person