869 Lims Jobs - Page 26

Greetings from TCS Recruitment Team ! Skill: SAP QM S/4 HANA Years of experience: 5 to14 Years Walk-In-Drive Location: Hyderabad Walk-in-Location Details: TCS Kohinoor Park Drive Time: 9 am to 1:00 PM JD Must have knowledge of quality notification, workflows. Must have worked on complex QM enhancements. Should have knowledge of QM interfaces like LIMS as well as IDOC, proxy. Handling of automatic Batch jobs in QM/defect management/deadline monitoring Must have worked on LSMW, should be able to handle QM data update and upload tasks. Troubleshoot and resolve issues related to the QM module Must have experience in process industry with strong knowledge of batch management Must be able to write good quality functional specification and quality testing documents. Strong knowledge of QM master data inspection plan, sample procedure/drawing procedure, class, characteristics, MIC, inspection types, certificate profile, DMR Show more Show less

Job Summary: Join us in shaping the future of EV battery manufacturing in Sanand, India! As a Systems Engineer – MES, you’ll play a key role in optimizing IT solutions that power manufacturing operations, ensuring seamless connectivity between production lines, quality control systems, and enterprise applications. This role is a unique opportunity to bridge technology and manufacturing, driving efficiency, minimizing downtime, and ensuring compliance with industry standards. You’ll collaborate across engineering, automation, and IT teams, integrating cutting-edge MES solutions that enhance performance and innovation in battery production. If you’re passionate about MES technology, system integration, and making an impact in the EV industry, this is the role for you! Key Responsibilities: Manufacturing IT Operations: · Configure Dassault Delmia Apriso MES for battery manufacturing workflows. · Be proactively involved in the MES solution design, development, implementation, support, and maintenance. · Ensure the MES is configured to represent all manufacturing workflows. · Collaborate with IT solution architects as a teams to translate business requirements into MOM capabilities. · Play a fundamental role to enhance MES-driven operations. System Integration: · Ensure seamless integration of MES with interfacing to OT systems (SCADA, WCS, Automation, IoT). · Enable MES connectivity with IT systems (ERP, PLM, LIMS, QMS, WMS) for real-time data flow. Project Management: · Ensuring timely delivery and milestone adherence of MES projects. Technical Ability: · Provide technical expertise in development, testing, and cross-functional team engagement. · Troubleshoot and resolve MES-related issues, driving continuous improvement initiatives. Documentation: · Update and maintain comprehensive functional and technical design documentation. · Document data workflows between manufacturing systems and enterprise applications. Training and Support: · Conduct training sessions and lead workshops for internal and external stakeholders. · Support MES system users to ensure smooth operations and optimal system utilization. Required Skills & Experience: · 6–12 months experience with MES solutions (essential). · Proven ability to configure MES and integrate with ERP, PLM, WMS & OT systems. · Strong proficiency in C# programming and SQL databases. · Experience in ISA-95 & ISA-88 standards for seamless system integration. · 3+ years' MES experience in battery, semi-conductor, life sciences, pharma, or biotech industries. · Project management expertise in MES implementation and equipment interface commissioning. Candidate Profile: · Bachelor’s/Master’s degree in Engineering, Computer Science, or a related field. · 3+ years’ industry experience, preferably in battery giga factories, semi-conductor, pharma, or biotech. · Strong collaboration, communication, and problem-solving skills for business-IT alignment. · Ability to work onsite in Sanand, Gujarat, in a fast-paced manufacturing environment. Show more Show less

15+ years of experience in SAP transformation, development, and AMS projects with at least 3 End-to-End implementation projects Business Process Knowledge of topics viz. Quality Planning, Quality inspection, Quality Control, Quality certificates, Quality Notifications, Stability Studies, Batch Management etc. Experience of integrating SAP QM with External system 3PLs like MES, Trackwise, LIMS, Labware, Lab Vantage etc., and with other SAP modules, GXP and SOX requirements Experience as Solution Architect in the multiple programs of global scale Experience in Business Blue Printing, Design, Prototyping, Functional Analysis, Configuration, Gap Analysis, Conversion, Migration, Testing, Training, Cutover, Go-Live and Post Go-live Support activities, driving Business process workshops and Fit/GAP analysis Deep Knowledge and expertise in Quality Management BPML Good experience in Data migration process and ETL Tools Lead the engagement efforts at different stages from Problem definition to diagnosis to solution design, development & deployment, contribute to unit level & Organizational initiatives. Design, Build & Optimize End to End SAP Quality Management Processes for customers enterprise. Engagement Life cycle Management Client Opportunity Identification and Proposal Development Client Relationship Management Talent Management Marketing and branding using Thought Leadership Deal Influencing, Negotiation and Closure IP Creation and Management Knowledge Management SAP QM (Quality Management) with Pharma & Process Industry experience. The candidate is expected to be a senior Functional Architect for SAP Programs and will anchor the engagement effort for assignments, all the way from business process consulting and problem definition to solution design, development, and deployment for S/4HANA Quality Management. You will lead business transformation programs helping clients mitigate Digitization related challenges. You will be pivotal to problem definition and discovery of the overall solution and guide teams on project processes, deliverables. You will have the opportunity to shape value-adding consulting solutions that enable our clients to meet the changing needs of the global landscape. Domain experience in Quality Management with S/4HANA certification (preferred). Experience in Deal Pricing & Transformation Deal Estimations, Ability to work with different tools like, Solman, Doc Nav, Sharepoint, Mercury QC etc. Sufficient ABAP, Fiori, Technical know-how to co-ordinate better with technical teams. Should have experience of Change Management, Task Planning, Project Reporting, Resource Management, Process Improvement, Supervising. Show more Show less

10+ year of experience in Design, configuration, testing, and deployment of LabWare Products Should have experience in design and implement interfaces with external applications Should have strong working experience of subroutines, LIMS Basic Experience in instrument integration with the LabWare products Interface with customer to gather User Requirements Provide consistent OOB designs for clients and avoid excessive use of LIMS Basic Be able to create and design blueprints for the conceptual system before any development or configuration begins Should have good experience in SQL. Should have the ability to develop complex queries and scripts. Should have good understanding of server architecture Good Experience in Crystal Reports. Be able to conduct code reviews of others against the LabWare configuration guidelines Participate in Gap Fit and provide inputs related to design and architecture Good communication knowledge Ability and willingness to work independently and with a team Train and mentor team members Show more Show less

Jun 5, 2025 Location: Pune Title: SAP PP : We are looking for an SAP QM (Quality Management) Consultant with 2-3 years of experience to join our team and support ongoing project requirements. The ideal candidate should have hands-on experience in implementing and supporting SAP QM processes and integration with other SAP modules. Key Responsibilities Configure and customize SAP QM module to align with business requirements. Manage quality processes including: Inspection Planning (IP) Quality Notifications Quality Inspection Lot Processing Results Recording and Defects Management Certificate Management Sample Management and Stability Studies Ensure proper integration of SAP QM with modules such as MM, PP, and SD. Troubleshoot and resolve issues related to quality processes in SAP. Collaborate with business users to gather requirements and implement solutions. Assist in end-user training and knowledge transfer activities. Participate in system testing, UAT (User Acceptance Testing), and post-go-live support. Prepare documentation, including functional specifications, test cases, and training materials. Support continuous improvement initiatives by recommending process enhancements. Required Skills 2-3 years of experience in SAP QM implementation, support, or rollout projects. Strong understanding of quality inspection processes and control mechanisms. Knowledge of master data management in QM, including material master, inspection plans, and catalogs. Experience in creating and processing inspection lots and quality notifications. Basic knowledge of integration points with MM (Materials Management), PP (Production Planning), and SD (Sales and Distribution). Strong problem-solving and analytical skills. Good communication skills and the ability to work with cross-functional teams. Preferred Skills Experience with SAP S/4HANA QM. Exposure to LIMS (Laboratory Information Management Systems) integration. Knowledge of regulatory compliance standards such as ISO and GMP. Qualification: Graduate No. of Job Positions: 2 Total Experience: 2-3 years Domain Experience: QM Show more Show less

Job Summary We are seeking an experienced Full Stack Engineer with 10 to 12 years of experience to join our team. The ideal candidate will have a strong background in LIMS and a good understanding of Bioinformatics. This hybrid role requires a deep technical expertise and the ability to work collaboratively in a dynamic environment. The position does not require travel and operates during day shifts. Responsibilities Develop and maintain full stack applications with a focus on LIMS integration. Collaborate with cross-functional teams to design and implement new features. Ensure the scalability and performance of web applications. Provide technical guidance and mentorship to junior developers. Conduct code reviews and ensure adherence to best practices. Troubleshoot and resolve complex technical issues. Work closely with stakeholders to gather and refine requirements. Implement security best practices to protect sensitive data. Stay updated with the latest industry trends and technologies. Contribute to the continuous improvement of development processes. Document technical specifications and project plans. Participate in agile ceremonies and contribute to sprint planning. Ensure the quality and reliability of software through rigorous testing. Qualifications Possess a strong background in LIMS with hands-on experience. Have a good understanding of Bioinformatics and its applications. Demonstrate proficiency in both front-end and back-end technologies. Exhibit excellent problem-solving and analytical skills. Show strong communication and collaboration abilities. Have experience with agile development methodologies. Be familiar with security best practices in software development. Hold a degree in Computer Science or a related field. Have a proven track record of delivering high-quality software solutions. Be adaptable and open to learning new technologies. Demonstrate the ability to work independently and as part of a team. Show a commitment to continuous improvement and professional development. Have experience with cloud platforms and services. Certifications Required Certified LIMS Professional Full Stack Web Development Certification Show more Show less

LABVANTAGE Job Description 4-13 years’ experience in LabVantage LIMS implementation experience of LV8.x projects Must have experience in requirement analysis and system designing. Must have hands on experience in configuration and/or coding in LabVantage. Strong understanding of SDLC & CSV methodologies Must have good communication skills and have experience in customer communication. Strong understanding of Oracle, PL/SQL Workable experience in Jasper reporting will be preferred. Proven team leader – ability to mentor team to deliver results Must be adept in at least: Java (J2EE), JavaScript, JSP, HTML, DHTML/Web Page Development including client-side scripting and SQL for relational databases (either Oracle and/or SQL Server) Other desirable technical skills include Web Service, Ajax, Groovy and J-Query System Analysis, in addition to domain knowledge of laboratory practices. Excellent problem-solving skills Ability to identify ways to continuously improve processes which will help in delivering superior solutions on time and in budget Show more Show less

Job Title: QC Executive – (RM / FG / Stability / AMV & PV / Microbiology) Location: Indore – Regulated Pharma Manufacturing Plant Department: Quality Control Reporting To: QC Manager / Head – Quality Control Job Type: Full-Time | Executive Level Job Purpose To perform quality control testing and analysis of raw materials, finished products, stability samples, and microbiological parameters as per current Good Manufacturing Practices (cGMP), standard operating procedures (SOPs), pharmacopeial standards, and regulatory requirements to ensure product quality and compliance. Key Responsibilities Testing and Analysis Perform chemical and instrumental testing of Raw Materials (RM) and Finished Goods (FG) as per pharmacopeial and in-house specifications. Conduct Stability Studies in line with ICH guidelines and maintain records of stability trends. Execute Analytical Method Validations (AMV) and support Process Validation (PV) testing. Carry out Microbiological analysis of samples, including environmental monitoring, water testing, and microbial limit tests. Documentation and Compliance Maintain accurate, complete, and timely documentation (analytical reports, logbooks, LIMS/ERP entries). Ensure compliance with cGMP, GLP, and regulatory standards (USFDA, EU-GMP, WHO, etc.) . Participate in internal audits, external regulatory inspections , and implement CAPAs. Prepare and review standard operating procedures (SOPs), specifications, and testing protocols. Equipment Operation & Calibration Operate and calibrate instruments like HPLC, GC, UV, IR, Dissolution Apparatus, FTIR, etc. Ensure timely preventive maintenance and validation of QC instruments. Cross-functional Coordination Coordinate with Production, QA, Regulatory Affairs, and other relevant departments to resolve testing issues and support product release timelines. Participate in investigations of OOS/OOT results, deviations, and change controls. Key Skills & Competencies Sound knowledge of cGMP/GLP and ICH guidelines. Hands-on experience with analytical instruments and microbiology techniques. Strong documentation and data integrity practices. Good communication and team collaboration skills. Eye for detail and high level of integrity. Educational Qualifications B.Pharm / M.Pharm / M.Sc. (Chemistry / Microbiology / Pharmaceutical Sciences) Experience 2–5 years of relevant experience in a regulated pharmaceutical manufacturing environment. Preferred Certifications Training in Data Integrity, cGMP, QMS, or Instrument Handling is an advantage. Show more Show less

🚀 We're Hiring! Software Sales and Implementation – Pragya LIMS 📍 Location: Ahmedabad (Work from Office) 🧪 Industry: Laboratory Information Management System (LIMS) 💼 Experience: 1-3 years in B2B Software Sales or Lab Industry Sales 📩 Apply at: info@pragyalims.com About Us: Pragya LIMS is a smart, scalable Laboratory Information Management System designed to digitize and streamline material testing lab operations. With clients across metallurgy, paint, pharma, and environment sectors, we’re redefining how labs operate in the digital age. We are looking for a passionate Software Sales and Implementation who can drive growth by connecting with testing labs, showcasing the value of our product, and building lasting client relationships. 🔍 Your Responsibilities: Identify and approach potential clients (testing labs, calibration labs, NABL-accredited labs). Conduct product demos and explain features tailored to client needs. Follow up on leads, inquiries, and referrals. Understand client pain points and prepare customized proposals. Negotiate pricing and close deals. Coordinate with the implementation team for smooth onboarding. Maintain CRM and report weekly sales activities. ✅ You Must Have: 1–3 years of experience in software sales, LIMS, or lab services. Strong communication and presentation skills. Ability to explain technical concepts in simple terms. Confidence to travel and visit client sites when needed. Fluency in English, Hindi, and Gujarati preferred. 🌟 Nice to Have: Experience with CRM tools (e.g., Zoho, HubSpot). Understanding of NABL, ISO 17025, or lab workflows. Tech-savvy mindset and proactive attitude. 🎯 Why Join Us? Be part of a growing company shaping the future of digital labs. Exposure to various lab domains and real-time impact. Freedom to contribute ideas and lead sales initiatives. Attractive incentives on successful closures. 📢 Ready to grow with us? Send your CV to info@pragyalims.com or DM us here. Tag someone who’d be a great fit! #Hiring #SalesJobs #AhmedabadJobs #LIMS #SoftwareSales #LabSoftware #PragyaLIMS #TechJobs #FieldSales #JobOpening Show more Show less

About SheKnowmics At SheKnowmics , we are building the future of women’s health — one smart pad, one data point, and one empowered woman at a time. Our mission is to make non-invasive, home-based molecular diagnostics for hormonal, reproductive, and sexual health accessible, stigma-free, and lightning fast — delivering lab-accurate results in 48 hours via innovative sample collection methods (smart pads, tampons, swabs, saliva, urine). Backed by deep expertise in genomics, diagnostics , and D2C healthcare , we are building a platform that empowers millions of women to take control of their health journeys from the comfort of home. We’re not just a product — we’re a movement to normalize intimate wellness through science, tech, and human-first design. The Role: Co-Founder & Chief Technology Officer (CTO) (With experience in D2C, digital health, or consumer tech) We’re looking for a mission-driven technologist and product visionary to join as Co-Founder & CTO — someone who can architect and lead the development of our D2C femtech platform from the ground up. You’ll be responsible for translating the vision of SheKnowmics into a scalable, secure, and beautiful digital experience , integrating home testing, lab logistics, AI-driven insights, and user-friendly design into one cohesive ecosystem. 🔧 Responsibilities Build & own the tech roadmap — from MVP to scale Develop the web/app platform for: Test kit booking and result tracking Symptom journaling and hormone/cycle insights Personalized health content and recommendations Architect secure systems for sample tracking , lab integrations , and LIMS sync Ensure data privacy and compliance (GDPR/HIPAA standards) Develop or integrate AI/ML models for pattern recognition in hormonal health and diagnostics Lead and build an engineering team as the company grows Work alongside the founding team on fundraising, pitch decks, and investor meetings Maintain tech budgets, vendor management, and scalable cloud infrastructure (AWS, GCP, etc.) ✅ You Bring 2–5 years of experience in software development , ideally with startup or D2C healthtech exposure Proven ability to build and launch full-stack consumer platforms Deep expertise in technologies like React/Next.js, Node.js, Python, Firebase, AWS/GCP Strong understanding of API architecture , user data flows , and 3rd-party integrations Bonus: Experience in digital health, LIMS, diagnostics, bioinformatics, or femtech Bonus: Familiarity with AI/ML tools (e.g. TensorFlow, scikit-learn) for health data interpretation Entrepreneurial mindset with a desire to co-own a high-impact femtech brand Grit, curiosity, and belief in breaking taboos around women’s wellness ❤️ Why You Should Join Be a co-founder in one of India's most promising femtech startups Build impactful tech that transforms how women access diagnostics Own a meaningful equity stake Collaborate with a visionary founder with a deep background in genomics, diagnostics, and D2C healthcare Lead tech in a greenfield opportunity — no legacy code, just bold ideas Help shape a brand that empowers 500M+ Indian women 📩 How to Apply Excited to build with purpose? Drop a message via LinkedIn and let’s reimagine diagnostics together. Show more Show less

JOB TITLE: Assistant Manager – R&D Processing, Home Care Bars LOCATION: Mumbai About Unilever 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. Role Purpose To lead the process design strategy for Home Care (HC) Bars, focusing on innovation, technology integration, and digital transformation. The role involves defining process specifications, establishing scale-up protocols, and ensuring seamless implementation across manufacturing platforms. Key Responsibilities Develop and execute Design of Experiments (DoE) to define material handling protocols and processing routes for innovation and cost-saving initiatives. Provide timely technical inputs across critical project workstreams. Lead manufacturing design lock for key technologies and ensure alignment with strategic objectives. Define safety foundations and proactively eliminate risks in accordance with the Safety in Manufacture and Supply Approval System (SIMAS) to secure project approvals. Drive capability building initiatives at AMC-Bars. Oversee installation and commissioning of plant equipment, author operating manuals, and conduct initial operator training. Collaborate with Supply Chain to evaluate and enhance return on investment (ROI) for projects. Ensure product quality through close coordination with Supply Chain teams. Conduct standard trials and tests for soaps and NSD bars at lab and pilot scales, supported by physical-chemical analysis. Plan, execute, and report main plant trials with comprehensive data analysis and technical documentation. Ensure adherence to Unilever’s safety and product standards. Conduct pilot-scale trials to define process and packaging specifications for new raw materials and blends. Validate plant-scale changes for impact on capacity, quality, and efficiency. Maintain system updates reflecting formulation changes (e.g., PFD Tool, BOMs). Identify recurring production issues and develop troubleshooting protocols. Draft and implement operating instructions (manuals and SOPs) and train trainers and operators on modified processes. Utilize digital tools such as Power BI, JMP, iProMPT, Pharos, LIMS, PLM, PFD, and CUC Finder to enhance process efficiency. Qualifications & Experience Bachelor’s degree in chemical engineering (BE/B.Tech/B.Sc). 5–7 years of experience in Research and Development, preferably in NSD Bars formulation and processing. Proficiency in digital tools for data modeling, process efficiency, and measurement. Strong knowledge of process control and mechanical instrumentation. Experience with HAZOPs and safety approval systems. Skilled in MS Office (Excel, PowerPoint, Word), SAP, and SCADA. Demonstrated project management and problem-solving capabilities. Understanding of consumer action standards and process parameter optimization. Stakeholder Engagement Internal Collaborate with Marketing, Supply Chain, Development, Production, and Project teams to ensure successful implementation of new products and technologies. External Engage with external partners to source advanced process technologies and integrate them into final design scopes. 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. Show more Show less

Primary Skills Strong expertise in SAP QM module implementation, configuration, and support within SAP S/4HANA or ECC. Experience in setting up inspection types, quality notifications, results recording, and usage decisions for incoming, in-process, and final inspections. Knowledge of quality planning, quality inspection, quality control, and quality certificates in manufacturing and procurement processes. Hands-on experience in integrating SAP QM with MM (Materials Management), PP (Production Planning), and SD (Sales & Distribution) for quality compliance. Expertise in quality management master data such as inspection plans, sampling procedures, catalogs, and characteristic control. Ability to configure vendor evaluation, supplier quality management, and audit management within SAP QM. Strong understanding of corrective and preventive actions (CAPA), deviation handling, and non-conformance management. Experience in quality notifications, complaint handling, and integration with SAP Workflow for approvals and corrective actions. Ability to troubleshoot and resolve SAP QM issues, optimize system performance, and provide end-user training. Secondary Skills Basic understanding of SAP EHS (Environment, Health, and Safety Management) for compliance reporting. Knowledge of statistical process control (SPC), Six Sigma, and Lean Quality methodologies. Experience with LIMS (Laboratory Information Management Systems) integration with SAP QM. Familiarity with automation tools, Fiori apps, and SAP Business Workflow for enhanced quality process management. Strong analytical and problem-solving skills for data analysis, reporting, and dashboard creation in SAP QM. Ability to work with cross-functional teams including production, procurement, sales, and regulatory compliance teams.

Job Summary (ISG) Lead Product Consultant Qualification Science / Engineering graduate Responsibility Pre Sales : Participate in the pre sales stage (eg preparation of marketing materials and collaterals, client calls, demos) proposals and business development activities to ensure functional expertise. Create solutions based on the customer needs and review estimates to prepare for RFIs and RFPs. Seek opportunities in mining the relationship to provide lasting value to the customer and share the same with the account team. Product Consulting Analyze and gather all requirements and manage the same across the project lifecycle to ensure the same are met during delivery. Conduct high level gap analysis / fitment analysis of requirements against product from the Cognizant portfolio. Arrive at possible solution alternatives that factor in gap resolution, impact on related technical areas, acceptability of the solution to the user community, technical feasibility and efficiency (based on experience, secondary research, inputs from other project case studies, and tweaking the available product capabilities). Translate the requirements into product customization requirements. Suggest implementation framework and methodology. Present the solution, Cognizant capabilities etc to the client. Provide demos to the customer on the products, when required. Project Management Interact with customers to identify customer expectations and ensure all customer issues are resolved appropriately. Prepare estimation guidelines. Review estimates and impact analysis, etcas prepared by the Senior Product Specialist. Prepare and track project plan. Perform key project management activities like planning, work allocation and tracking, endtoenddelivery, daytoday interaction with onsite, status reporting, performance reporting, quality assurance activities, etc. Maintain documentation (eg defect prevention checklist, metrics etc). Work with the various track leads to ensure delivery. Discuss and resolve feasibility issues with the customer. Design And Implementation Participate and provide inputs in design and architecture reviews with the technical team. Review all deliverables as per the delivery checklist. Participate in product configurations. Testing Provide QA and UAT support from a functional perspective to the Testing team. Innovation Collate, centralize & institutionalize all solution enablers developed by individual projects. Identify the learning’s and opportunities during the course of the project. Identify artifacts which can be reused across multiple projects. Capability Building Create material for product certifications, under guidance. Contribute to training sessions. Prepare summary & detailed case study for the project. Knowledge Management (When allocated)Act as a domain SME, conduct domain centric sessions/ product knowledge sessions within PPS. Review KM process and artifacts to ensure the same is updated based on current trends, projects and consulting engagements. People Management Analyze team’s capabilities (SWOT) and allocate work efficiently. Resolve conflicts within team members. Support team building activities. Provide administrative support. Provide inputs on goal setting and performance appraisal of team. Identify skill gaps and training needs as required. Provide input into the learning and career plans for team members. Identify training needs of team members and provide coaching support to them. Mentor team. Nominate team for awards. Conduct training through academy and induction of new team members. Must Have Skills Any LIMS LIMS - Labware LabVantage Show more Show less

Job Summary: The Lab Technician (Phlebotomist) is responsible for collecting, handling, and processing blood samples for laboratory diagnosis. This role requires precision in venipuncture, proper sample handling, and adherence to safety protocols to ensure accurate test results and patient safety. Key Responsibilities: 1. Blood Collection: Perform venipuncture and capillary blood collection from patients following proper techniques and safety protocols. 2. Sample Handling & Processing: Label, store, and transport blood samples as per laboratory guidelines. 3. Patient Interaction: Communicate effectively with patients, ensure their comfort, and address concerns regarding sample collection. 4. Equipment Maintenance: Maintain and sterilize phlebotomy instruments and ensure their proper functioning. 5. Documentation & Record-Keeping: Properly document patient details, test requests, and sample tracking in laboratory management systems. 6. Safety & Compliance: Follow biosafety and infection control guidelines as per Indian regulations. 7. Quality Assurance: Adhere to standard operating procedures (SOPs) and laboratory best practices to minimize errors. 8. Coordination: Work closely with laboratory technicians, pathologists, and other healthcare professionals for smooth operations. Required Qualifications & Certifications (As per Indian Law) Educational Qualification: Diploma in Medical Laboratory Technology (DMLT) (2 years) Bachelor in Medical Laboratory Technology (BMLT) (3 years) Certificate Course in Phlebotomy (6 months – 1 year) (Optional but recommended) Certifications & Licensing: 1. State/ National Certification: Certification from a recognized medical laboratory training institute 2. Registration with State Paramedical Council (varies by state) 3. Registration with the All India Institute of Medical Technologists (AIIMT) (if applicable) Skills & Competencies Required: 1. Expertise in venipuncture and sample collection 2. Knowledge of laboratory safety protocols 3. Attention to detail and accuracy 4. Strong interpersonal and communication skills 5. Ability to handle stressful situations with empathy 6. Proficiency in using laboratory software (LIMS) Work Environment: 1. Hospitals, diagnostic laboratories, Clinics, or research institutions 2. Requires wearing protective gear (gloves, masks, lab coats) 3. Standing for long hours and handling biological samples 4. Travel required for home visits and mobile sample collection services Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹18,000.00 per month Benefits: Leave encashment Paid sick time Paid time off Ability to commute/relocate: Sri Nagar Colony, Hyderabad, Telangana: Reliably commute or planning to relocate before starting work (Preferred) Education: Diploma (Preferred) Experience: Clinical laboratory: 4 years (Preferred) Willingness to travel: 50% (Preferred) Work Location: In person

PATH current employees - please log in and apply Here PATH is a global nonprofit dedicated to achieving health equity. With more than 40 years of experience forging multisector partnerships and with expertise in science, economics, technology, advocacy, and dozens of other specialties, PATH develops and scales up innovative solutions to the world’s most pressing heath challenges. About The Project The Ministry of Health and Family Welfare (MoHFW) has launched a dedicated Metropolitan Disease Surveillance Strengthening component under the Pradhan Mantri Ayushman Bharat Health Infrastructure Mission (PM-ABHIM). Covering 20 cities across India, this initiative is supported by the World Bank through the Transforming India’s Public Health Systems for Pandemic Preparedness Program (PHSPP). PATH has been selected as a key partner in establishing a Technical Support Unit (TSU) to provide expert guidance in the design and implementation of this initiative. The TSU will provide strategic direction and technical support for the initial two years of the program, leveraging global experience and best practices to strengthen metropolitan disease surveillance. The primary objective is to facilitate operationalization, address challenges, and promote innovations as global public goods. Position Overview PATH is seeking for Public Health Laboratory Expert on Third Party Payroll- (Randstad). The Public Health Laboratory Expert will play a pivotal role in guiding the strategic implementation, monitoring, and enhancement of the metropolitan disease surveillance program. This role involves close collaboration with national health authorities, stakeholders, and technical partners to ensure the success and sustainability of the program. The Consultant will lead efforts to improve public health laboratory infrastructure, enhance quality assurance processes, and strengthen laboratory-based surveillance across metropolitan cities. Duty Location : National Centre for Disease Control, Delhi Key Roles And Responsibilities Laboratory Infrastructure Assessment: Conduct assessments of public health laboratory infrastructure, staffing, and capabilities across selected metropolitan cities. Draw on the global best practices to provide recommendations for improvement and modernization. Private Sector Engagement: Develop strategies to enhance private sector participation in laboratory-based disease surveillance, including options for integration with public health systems and improving collaboration between stand-alone laboratories, hospital-attached laboratories, and national networks. Quality Assurance and Standards: Evaluate existing laboratory quality assurance systems and develop actionable plans to address critical gaps. Introduce global best practices to strengthen laboratory standards, protocols, and accreditation processes. Training and Capacity Building: Design and implement training programs for laboratory personnel to ensure adherence to national and international standards, with a focus on quality control, biosafety, and emerging disease diagnostics. Coordination and Technical Support: Work closely with state and national health agencies, including the Integrated Disease Surveillance Program (IDSP) unit of the National Centre for Disease Control (NCDC), to provide technical support and strategic direction for laboratory surveillance initiatives. Data Integration and Reporting: Support the integration of laboratory data into national surveillance systems, ensuring timely reporting and the use of laboratory data for public health decision-making. Policy and Advocacy: Contribute to the development of national policies and guidelines for laboratory-based disease surveillance, ensuring alignment with global standards and promoting sustainability. Qualifications And Experience Education: Master’s degree in microbiology, Molecular Biology, or a related field. A PhD in Microbiology or an MD in Microbiology would be preferred. Experience: Minimum of 10 years of experience in public health laboratory systems, with a strong background in disease surveillance, antimicrobial resistance (AMR), and infectious diseases, particularly in urban settings. Expertise: Proven expertise in public health infrastructure, laboratory quality assurance, and private sector engagement in laboratory-based surveillance. Partnerships: Experience working with national and state health agencies, including NCDC, IDSP, and NACO as well as with international partners such as WHO and CDC. Essential Skills Communication: Exceptional verbal and written communication skills in English and Hindi, with the ability to convey complex technical information clearly and effectively. Project Management: Strong organizational and project management skills, with a proven ability to manage multiple tasks and deadlines efficiently. Technical Proficiency: Proficiency in MS Office (Word, Excel, PowerPoint, Outlook) and familiarity with laboratory information management systems (LIMS) and digital tools for data analysis. Stakeholder Engagement: Demonstrated ability to work collaboratively with government counterparts, donors, and development partners at both national and state levels. Health Systems Knowledge: Deep understanding of India’s health system, particularly in the context of disease surveillance initiatives such as IHIP, IDSP, and key national programs like NHM, Ayushman Bharat, PM-ABHIM (specifically IPHL and BPHU component), and the XV-FC. Flexibility: Willingness to travel up to 30% of the time for program-related activities. Location: Delhi Show more Show less

Job Title: Technical Manager (Mechanical Lab) Location: Ahmedabad Company: Industrial Testing Center Private Limited Employment Type: Full-time About Us: Industrial Testing Center Private Limited is a NABL-accredited laboratory specialising in mechanical testing and quality assurance services for various industries. We are committed to delivering accurate and reliable test results while maintaining the highest standards of integrity and professionalism. Job Summary: We are seeking an experienced Senior Testing Engineer to oversee testing operations, ensure compliance with international standards, and manage laboratory equipment. The ideal candidate will have extensive hands-on experience in mechanical testing within a NABL-accredited lab and a strong understanding of ASTM, API, ISO, and IS standards. Key Responsibilities: Perform and supervise mechanical tests including tensile testing, hardness testing, Charpy impact testing, proof load testing, and pull-off adhesion testing in compliance with applicable standards. Ensure all testing procedures adhere to NABL accreditation requirements and maintain documentation for audits. Handle third-party inspector calls and coordinate with clients for testing requirements. Oversee maintenance, calibration, and troubleshooting of testing equipment to ensure accuracy and reliability. Interpret test results, prepare detailed reports, and provide technical recommendations. Stay updated with ASTM, API, ISO, IS, and other relevant standards related to material and mechanical testing. Train and mentor junior technicians and engineers in testing methodologies. Implement quality control measures to enhance laboratory efficiency. Qualifications & Skills: Diploma or Bachelor’s degree in Mechanical Engineering. Minimum 5 years of experience in a NABL-accredited testing laboratory. Hands-on expertise in tensile, hardness, impact, proof load, and adhesion testing. Strong knowledge of ASTM, API, ISO, and IS standards for mechanical testing. Experience in equipment maintenance, calibration, and handling third-party audits. Excellent analytical, problem-solving, and reporting skills. Ability to work independently and lead a team. Preferred Attributes: Certification in NABL auditing/testing procedures. Familiarity with laboratory information management systems (LIMS). Strong communication skills for client interactions. Why Join Us? Opportunity to work in a NABL-accredited lab with advanced testing facilities. Career growth in a technically challenging and quality-driven environment. Competitive salary and benefits package. How to Apply: Interested candidates may send their updated resume to info@itcpllab.com with the subject line "Application for Technical Manager (Mechanical Lab) – [Your Name]." Industrial Testing Center Private Limited is an equal-opportunity employer. Show more Show less

We are hiring an MSc/Postgraduate professional in Microbiology/Chemistry/Product Development for our Faridabad-based team! Key Responsibilities: 1. Conduct microbiological & chemical analysis of raw materials, in-process, and finished products. 2. Perform microbial testing (e.g., TVC, pathogens), media prep, and aseptic sampling. 3. Support new product development, improve formulations & perform stability, efficacy & shelf-life studies. 4. Maintain lab records, perform data logging (LIMS), statistical analysis & reporting. 5. Ensure QC/QA compliance with ISO, GMP, GLP; troubleshoot lab issues. 6. Operate & maintain lab instruments (pH meter, spectrophotometer, autoclave, etc.). 7. Follow lab safety & regulatory protocols; manage waste disposal. 8. Stay updated with research trends & share knowledge. ✅ Requirements: 1. MSc in Microbiology/Chemistry/Biotech/Biochem with 1+ yrs experience 2. Strong lab skills, product development exposure, and data analysis proficiency Location: Faridabad Apply now: vikas@triindia.org Job Types: Full-time, Permanent, Fresher Pay: ₹15,000.00 - ₹30,000.00 per month Benefits: Health insurance Leave encashment Provident Fund Schedule: Day shift Fixed shift Weekend availability Work Location: In person

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 Job Summary We are seeking an individual to lead the stability samples receipt and planning the analysis of stability samples, manage incidents and investigations, approve documents, and ensure laboratory compliance with practices and cleanliness. The role involves procurement of laboratory requirements, instrument qualifications, and calibration. Roles & Responsibilities Responsible to follow good laboratory and safety practices in the laboratory. Responsible to follow good documentation practices in the laboratory. Responsible to ensure the cleanliness of the laboratory. Responsible to participate and organize equipment/instrument Qualifications & change control mechanism. Responsible to ensure that all the equipment's and instruments are in validated and calibrated state. Responsible to ensure calibration/ performance verification of analytical Instruments and equipment's as per master schedule. Responsible for planning of In-process (IP), Finished Product (FP) and Stability sample analysis with respect to Nasal spray products through Manual/SAP/LIMS. Responsible for planning of packaging material activities with respect to Nasal spray product through Manual/SAP/LIMS. Technical knowledge , Calibration and operation of Spraytec, Sprayveiw for spray pattern , microscope and viscosity. Responsible to ensure the completion the stability sample analysis within the window period. Responsible to ensure stability studies are executed as per approved stability protocol. Responsible to initiate, investigate and review of incidents, OOS and OOT. Responsible to initiate, review and approval of CRN. Responsible for review of analytical documents. Responsible for approval of STPs, Specifications, SOPs, protocols and Analytical test reports. Responsible to ensure and maintain laboratory analytical standards as per the laid down procedures. Responsible to review and update reference standards against updated catalogues online. Responsible for procurement of laboratory requirements. Responsible to evaluate the instrument/Equipment breakdown as per laid down procedure. Responsible for preparation of response for internal and external audits and other QMS related activities. Responsible for review and approval of record of analysis and analytical test report. Responsible to ensure that the deactivation or destruction of samples as per laid down procedures. Responsible to review and approval the protocols, reports, specification and standard test procedure. Responsible to ensure the implementation of the "Training Program and ensure proper compliance and to train new recruits and impart trainings as a qualified trainer. Responsible to ensure compliance in LIMS related activity and carry out the activities through LIMS (wherever applicable). Responsible to organize contract laboratory audits and certification. Responsible to ensure all the QMS documents like OOS, OOT, and Incident are timely investigated, reviewed and appropriate CAPA's are taken and implemented. Qualifications Educational qualification: An M.Sc. degree in Chemistry, Analytical Chemistry, or a related field Minimum work experience : 10 to 15 years of experience Skills & attributes: Technical Skills Knowledge of calibration and performance verification of analytical instruments and equipment as per the master schedule. Experience in ensuring the maintenance, preparation, and procurement of laboratory standards, chemicals, and solvents according to established procedures. Participation and organization of equipment/instrument qualifications and change control mechanisms. Procurement expertise for laboratory requirements. Behavioural Skills Attention to detail and commitment to ensuring compliance with QMS documents, including OOS, OOT, and Incident investigations. Ability to respond to internal and external audits and participate in other QMS-related activities. Strong organizational skills for LIMS related activities. Effective communication and collaboration skills for coordinating and implementing CAPAs. Additional Information About the Department Global Manufacturing Organisation (GMO) At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future. 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

Quality Control Analyst – Chemical Industry Gait Naurish (I) Ltd. Location: Sector 155, Noida, Uttar Pradesh Salary: ₹300,000 – ₹400,000 per annum Experience: Minimum 1 years in a chemical/QC laboratory environment Company Overview Gait Naurish (I) Ltd. is a leading fine‐chemicals and flavour intermediate synthesis company, specializing in developing and manufacturing high‐purity compounds for the food, fragrance, and nutraceutical industries. We are committed to innovation, quality, and regulatory compliance, with state‐of‐the‐art laboratories and pilot‐plant facilities in Noida. Position Summary We are seeking a meticulous and proactive Quality Analyst Chemist to join our Quality Control team. The ideal candidate will perform routine and advanced analytical tests to ensure that all incoming raw materials, in‐process samples, and finished products meet predefined quality and regulatory standards. Key Responsibilities Analytical Testing Conduct and interpret chromatographic analyses using GC (Gas Chromatography) and HPLC (High-Performance Liquid Chromatography). Perform moisture determination via Karl Fischer titration. Execute TLC (Thin-Layer Chromatography) for rapid qualitative assessments. Method Development & Validation Assist in developing, optimizing, and validating new analytical methods in accordance with ICH and USP guidelines. Maintain method documentation, standard operating procedures (SOPs), and validation reports. Quality Assurance Support Review raw data and prepare analytical reports with clear interpretations. Investigate non‐conformities, deviations, and out‐of‐specification (OOS) results; propose corrective actions. Participate in internal and external audits; ensure compliance with GLP/GMP standards. Laboratory Maintenance & Safety Calibrate, maintain, and troubleshoot analytical instruments (GC, HPLC, Karl Fischer apparatus, TLC chambers). Monitor laboratory consumables, reagents, and standards; ensure proper storage and inventory control. Adhere to safety protocols, chemical handling procedures, and waste‐disposal guidelines. Qualifications & Experience Educational Background: Bachelor’s or Master’s degree in Chemistry, Analytical Chemistry, or a related discipline. Professional Experience: At least 1 years of hands‐on experience in a QC/analytical laboratory within a fine chemicals, pharmaceutical, or related industry. Technical Expertise: Proven proficiency in GC and HPLC operation, sample preparation, and data analysis. Demonstrated experience with Karl Fischer titration and TLC techniques. Familiarity with chromatographic software (e.g., Empower, ChemStation) and LIMS is a plus. Soft Skills: Strong attention to detail, analytical mindset, and problem‐solving ability. Excellent documentation, report‐writing, and communication skills. Ability to work both independently and collaboratively in a fast‐paced environment. What We Offer Competitive salary and performance‐based incentives Comprehensive health insurance and statutory benefits Opportunities for professional development and training A collaborative work culture in a cutting‐edge R&D and manufacturing environment Application Process Interested candidates may send their CV and a cover letter detailing relevant experience to hrm@fnni.in with the subject line “Quality Analyst Chemist – Sector 155, Noida” Job Type: Full-time Pay: ₹300,000.00 - ₹400,000.00 per year Benefits: Health insurance Paid sick time Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person Application Deadline: 15/06/2025

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Manager - Corporate Quality Audit Date: May 19, 2025 Location: Bangalore - Plant Company: Sun Pharmaceutical Industries Ltd Sun Pharma Corporate Quality Department Position: Manager (G10) Effective Date: Department: Corporate Quality Location: Bengaluru, Reporting Manager Title: GM - Corporate Quality Classification: Manager – Corporate Quality (Gamma Irradiation) Job Summary: Manager Corporate Quality – Individual Performer Role Responsible for oversight of Gamma Irradiation of Sun Pharma products at third party gamma irradiation sterilization. Essential Job Functions: Should possess sound knowledge of pharmaceutical manufacturing process (Non-sterile & Sterile formulations) & quality assurance regulations and auditing technique. Responsible for the overall supervision of Gamma sterilization site (Third party) used for sterilization of drug product and other components, as required. To monitor receipt and dispatch of consignment of Sun Pharma at Gamma sterilization site. Review and monitoring of irradiation process of the batch and related documentation. Review and monitor of analytical data (Dosimeter Testing) Control and monitor quality systems which enable operations on site to occur in an efficient manner and in compliance with cGMPs. Follow-up for timely closure of QMS documents. Participating in the investigations for Deviations, OOS and Audit findings related to Sun Pharma product/s. Review of changes in gamma sterilization process / major modification at site and timely notification to the management. Supporting in external audits preparations and responding to audit findings of gamma serialization sites Should be able to travel to third party site/s. Basic computer skills (Microsoft word/ Excel/ Power point presentation) and ability to learn and become proficient with appropriate software. Should possess good verbal and written communication skills. Basic Qualification: B. Pharm / MSc Industrial Experience & Knowledge: Minimum work experience of 10-15 Years in formulation & quality systems management operations. Exposure to regulatory agencies audits such as Schedule - M, USFDA, MHRA, ANVISA, TGA, WHO, ISO etc. Knowledge of Track wise/LIMS/SAP is desirable. Ability to work effectively in multicultural matrix organization. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Quality Control Analyst – Chemical Industry Gait Naurish (I) Ltd. Location: Sector 155, Noida, Uttar Pradesh Salary: ₹300,000 – ₹400,000 per annum Experience: Minimum 1 years in a chemical/QC laboratory environment Company Overview Gait Naurish (I) Ltd. is a leading fine‐chemicals and flavour intermediate synthesis company, specializing in developing and manufacturing high‐purity compounds for the food, fragrance, and nutraceutical industries. We are committed to innovation, quality, and regulatory compliance, with state‐of‐the‐art laboratories and pilot‐plant facilities in Noida. Position Summary We are seeking a meticulous and proactive Quality Analyst Chemist to join our Quality Control team. The ideal candidate will perform routine and advanced analytical tests to ensure that all incoming raw materials, in‐process samples, and finished products meet predefined quality and regulatory standards. Key Responsibilities Analytical Testing Conduct and interpret chromatographic analyses using GC (Gas Chromatography) and HPLC (High-Performance Liquid Chromatography). Perform moisture determination via Karl Fischer titration. Execute TLC (Thin-Layer Chromatography) for rapid qualitative assessments. Method Development & Validation Assist in developing, optimizing, and validating new analytical methods in accordance with ICH and USP guidelines. Maintain method documentation, standard operating procedures (SOPs), and validation reports. Quality Assurance Support Review raw data and prepare analytical reports with clear interpretations. Investigate non‐conformities, deviations, and out‐of‐specification (OOS) results; propose corrective actions. Participate in internal and external audits; ensure compliance with GLP/GMP standards. Laboratory Maintenance & Safety Calibrate, maintain, and troubleshoot analytical instruments (GC, HPLC, Karl Fischer apparatus, TLC chambers). Monitor laboratory consumables, reagents, and standards; ensure proper storage and inventory control. Adhere to safety protocols, chemical handling procedures, and waste‐disposal guidelines. Qualifications & Experience Educational Background: Bachelor’s or Master’s degree in Chemistry, Analytical Chemistry, or a related discipline. Professional Experience: At least 1 years of hands‐on experience in a QC/analytical laboratory within a fine chemicals, pharmaceutical, or related industry. Technical Expertise: Proven proficiency in GC and HPLC operation, sample preparation, and data analysis. Demonstrated experience with Karl Fischer titration and TLC techniques. Familiarity with chromatographic software (e.g., Empower, ChemStation) and LIMS is a plus. Soft Skills: Strong attention to detail, analytical mindset, and problem‐solving ability. Excellent documentation, report‐writing, and communication skills. Ability to work both independently and collaboratively in a fast‐paced environment. What We Offer Competitive salary and performance‐based incentives Comprehensive health insurance and statutory benefits Opportunities for professional development and training A collaborative work culture in a cutting‐edge R&D and manufacturing environment Application Process Interested candidates may send their CV and a cover letter detailing relevant experience to hrm@fnni.in with the subject line “Quality Analyst Chemist – Sector 155, Noida” Job Type: Full-time Pay: ₹300,000.00 - ₹400,000.00 per year Benefits: Health insurance Paid sick time Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person Application Deadline: 15/06/2025

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Sr.Officer LIMS (Master Data Reviewer) Date: May 30, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd Job Responsibilities: JOB DESCRIPTION- LIMS Masterdata Reviewer (Sr. Officer) To have thorough knowledge and understanding of QC workflows (Analysis/ Review/ Approve/ Investigation etc.), Analytical methods (Instrumental/ Pharmacopoeial chapters/ Monographs), QC instrumentation activities (operation, calibration, preventive maintenance etc.) and Analytical method validation/Method transfer activities and other processes of QC. To have thorough knowledge and understanding of Analysis reporting requirements of all stages of product for eg, but not limited to; Finished product, API, Excipients, Process validation, Hold time, Swab/rinse samples, Stability including result reporting, trending, COA requirements etc. To support for timely execution and completion of Masterdata activities. To ensure Masterdata creation and review as per established procedures and ensure updation of masterdata as per the observations, if any. To list down observations for any discrepancies found during creation/review of masterdata and share to respective team for resolution. To handover reviewed Masterdata for further process and keep track of closure of observations, if any. To track Masterdata activity status for creation, review and observation closure etc. To coordinate masterdata change management to ensure ongoing compliance with business and regulatory requirements. To have good hands on MS office (i.e. Word / Excel / Power Point) and other computer skills Education Qualification : M.Sc / B.Sc / B.Pharm Experience - 5 To 6 Yrs Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Sr. Manager - Micro Lead Date: Jun 3, 2025 Location: Ahmednagar - Quality Control Company: Sun Pharmaceutical Industries Ltd Job Title: Manager / Sr.Manager – Micro Lead Job Grade: G10 / G9B Function: Global API Business Sub-function: Manager’s Job Title: Skip Level Manager’s Title: Function Head Title: Location: Ahmednagar No. of Direct Reports (if any) Areas of Responsibility To plan, review and monitor overall activities in Microbiology and lead the department. Co-ordination with other departments for priorities and provide the timely support/testing to avoid delay due to analysis. Review of all departmental related documents and review results in LIMS system in microbiology section. Ensure all documents are complete in time. To review the lysate sensitivity test, Bacterial endotoxin test of WFI and API products. To check method validation of bacterial endotoxin test and microbial quality of products. To procure, receipt, storage, maintenance, its use and reconciliation of biological indicator, media, reagents standard cultures and bioball etc. To ensure and check calibration and Operation of TOC analyzer Execute breakdown (If any) in consultation with vender. To ensure environmental monitoring activities performed as per schedule and to check the environmental monitoring reports. To review qualification, Calibration of all instruments in microbiology laboratory as per SOP/Schedule. To participate in investigation and to review of deviations/OOS/OOT/OOC/Lab Event / & review of SOPs as per revision date in micro section online in track wise system. To highlight observations, rejection / failure, quality related concern in time and contribute in troubleshooting To ensure and review all logbooks and registers are maintained on line and available at designated place. Preparation and review of GMP documents related to activities. To review and ensure fumigation activity and its verification as per SOP/Guidelines. To prepare / review trends for water and environment monitoring, Summary report of water and environment monitoring. Responsible to follow online good documentation practices for data recording and monitoring. To ensure and review validation of autoclave, Dry heat sterilizer (DHS), Incubators, Laminar Air flow, HVAC. To ensure and review preparation of reagents and volumetric solution and its standardization as per specification / SOP. To ensure and review inventory and stock record of media/reagents/culture/lysate/CSE/LRW. To ensure to follow the GLP as per current practice in the laboratory. To ensure safety and use of personnel protective equipment’s during day to day activities Responsible for carrying out any other responsibilities assign from time to time orally or in writing by Quality head, however related training imparted to concerns. To support for review and compliance activity in quality function and to support for any time readiness as well as enhancement of system and practices. To Coordinate with corporate functions with respect to microbiology activity. Travel Estimate Job Requirements Educational Qualification M.Sc (Microbiology) Specific Certification Skills Experience 15 to 18 Yrs Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Manager Corporate Quality Projects Date: May 19, 2025 Location: Ahmednagar - Plant Company: Sun Pharmaceutical Industries Ltd Position: Manager-1 - Corporate Quality Projects Grade: G10 Education: M.Sc / B.Pharma / M.Pharma Job Location: Vadodara Job Profile: LIMS Lead is responsible for To have good experience & exposure of LIMS System implementations (Project developments support, validation, enhancements & implementations) across various site To ensure the dynamics of computerized systems w.r.t regulatory standards (21 CFR part 11, EU Annexure 11, & GAMP 5). To have good experience & exposure of SAP-HANA system, well aware of SAP system functionality. To have very good experience & expertise of Quality Control Systems & process (Functional expertise on sample management & Stability programme) To have very good experience & expertise of Quality Assurance process. To have knowledge of Quality control instruments handlings like HPLC, GC & UV for Sample Managements (Testing), Test Calculations (as per pharmacopeia general chapters & Monographs) & good understanding of Test different-different scenarios (like Dissolution & CU) for fate value check (Pass/fail) To provide guidance/Support sites for all the major regulatory audits by Remotely & Onsite visit Evaluation, assessments of different business requirements received, it’s impact assessments and decision for its consideration for digitization, simplification & automations. To identify the roadblocks and ensure the smooth execution of assigned projects. Responsible to ensure smooth functioning of the team operations and routine activities. Encouraged and developed the subordinates to explore their capabilities and take challenge to grow further. To identify the actionable and accomplish the project milestone. To prepare and review CSAP, qualifications scripts and ensure execution of qualification. To prepare, ensure and support for the preparation of database and design as per compliance requirements and functional needs. To ensure technical training / support for each site, whenever required. To ensure successful handover of projects to Site/Sites & support site SME’s for Stabilization of projects at sites. To conceptualize and frame a consolidated approach for new identified technique. To ensure vendor support for technical discussion on finalize of projects. To perform the activities as per the project plan / assigned scheduler. To execute, support other Quality project initiated for simplification, harmonization and productivity enhancement. To work in collaboration with IT, API, SGO, vendor, Site Quality and different teams for identification of the right solution /tool/Vendor, to resolve the “Specific problem” and have correct solution for the organization. Basic Expectation Candidate should Have a balance of technical knowledge & managerial skills Be able to prioritize & multi -task Be able to work independently with limited supervision Manage stakeholders & get work done Be able to create project plans/Charters which is efficient from a time, cost & effort perspective, while understanding at the long term impact of decisions Analytical & Report Creation Skills - Proficiency in Excel, Word & PowerPoint. Basic understanding of MySQL & Oracle database Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Micro Lead - API Date: May 16, 2025 Location: Ahmednagar - Quality Control Company: Sun Pharmaceutical Industries Ltd Job Description Title: Micro Lead API Location: Ahmednagar Grade: G9B- Sr. Manager 2 JOB RESPONSIBILITIES To plan, review and monitor overall activities in Microbiology and lead the department. Co-ordination with other departments for priorities and provide the timely support/testing to avoid delay due to analysis. Review of all departmental related documents and review results in LIMS system in microbiology section. Ensure all documents are complete in time. To review the lysate sensitivity test, Bacterial endotoxin test of WFI and API products. To check method validation of bacterial endotoxin test and microbial quality of products. To procure, receipt, storage, maintenance, its use and reconciliation of biological indicator, media, reagents standard cultures and bioball etc. To ensure and check calibration and Operation of TOC analyzer Execute breakdown (If any) in consultation with vender. To ensure environmental monitoring activities performed as per schedule and to check the environmental monitoring reports. To review qualification, Calibration of all instruments in microbiology laboratory as per SOP/Schedule. To participate in investigation and to review of deviations/OOS/OOT/OOC/Lab Event / & review of SOPs as per revision date in micro section online in track wise system. To highlight observations, rejection / failure, quality related concern in time and contribute in troubleshooting To ensure and review all logbooks and registers are maintained on line and available at designated place. Preparation and review of GMP documents related to activities. To review and ensure fumigation activity and its verification as per SOP/Guidelines. To prepare / review trends for water and environment monitoring, Summary report of water and environment monitoring. Responsible to follow online good documentation practices for data recording and monitoring. To ensure and review validation of autoclave, Dry heat sterilizer (DHS), Incubators, Laminar Air flow, HVAC. To ensure and review preparation of reagents and volumetric solution and its standardization as per specification / SOP. To ensure and review inventory and stock record of media/reagents/culture/lysate/CSE/LRW. To ensure to follow the GLP as per current practice in the laboratory. To ensure safety and use of personnel protective equipments during day to day activities Responsible for carrying out any other responsibilities assign from time to time orally or in writing by Quality head, however related training imparted to concerns. To support for review and compliance activity in quality function and to support for any time readiness as well as enhancement of system and practices. To Coordinate with corporate functions with respect to microbiology activity. Education : Graduates - Microbiology/ Equivalent ( experience In Micro testing / leading ) Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less