2502 Lims Jobs - Page 8

Job description: Job Title: Assistant Manager – Quality Lab (Need only Male candidate) Location: Sahibabad / Jewar / Greater Noida Experience: 8–10 Years Qualification: M.Sc. (Chemistry) / B. Tech (Chemical Engineering) Industry: Polymer / Plastic / Masterbatch / Compounding / Petrochemical Job Type: Full-Time | On-Site Role Objective: To lead the Quality Control Laboratory, ensuring accurate testing, equipment handling, and quality compliance in line with industry standards for polymers and plastics. Key Responsibilities: Manage and supervise all day-to-day activities of the Quality Lab (Raw Materials, In-process & Finished Goods testing). Operate, calibrate, and maintain all major lab inst...

Role Clarity: Business Development Manager Reporting To : Zonal Sales Manager Role Definition The Business Development Manager is responsible for driving growth by identifying and acquiring new customers within the zone. This role involves prospecting, customer profiling, building relationships, and promoting the organization's brand and services to achieve sales targets and expand the market. Deliverables Market Research and Analysis Customer Acquisition and Pipeline Development Customer Relationship Management Sales Process Management Reporting and Performance Analysis Key Responsibilities Prospecting and Customer Acquisition: Conduct market research in the zone to identify industry trends...

Hands-on experience on testing tools like HP ALM, Kneat and SNOW - Experience to MES, QMS (Trackwise), Lab solutions i.e. LIMS, Empower CDS, Chromeleon, Business Analytics, Middle wares etc. will be an advantage - OT System Qualification (Radio ligand Therapy or critical dosage forms will be a plus) - PAS/DCS Qualification - ISA95 High level of understanding - OT Security will be a plus. - Standalone Systems Qualifications - PAS/DCS Integrated with Manufacturing Equipment qualification. Key components of the responsibilities are as mentioned below but not limited to:  6+ yrs. of Professional experience and strong knowledge with real time experience in IT Quality & Compliance, Computer Syste...

Role & responsibilities Serve as the primary subject matter expert for all bioanalytical methods, including method development, validation, and sample analysis. Design and execute complex experiments for the quantification of drug candidates, metabolites, and biomarkers in biological matrices using a variety of platforms (e.g., Ligand Binding Assays, cell-based functional assays). Lead the evaluation, implementation, and troubleshooting of new analytical platforms and technologies to advance the laboratory's capabilities. Develop and influence bioanalytical strategies for multiple projects across the drug development pipeline. Manage project timelines and resources, serving as the bioanalyti...

Strong skills in Core Java, J2EE, , JavaScript, JSP, and DHTML/Web Page development. Experience in Labvantage LIMS development Strong relational database knowledge and experience using either Oracle and/or SQL Server.

The Clinical Laboratory Biochemist is responsible for performing biochemical analyses on patient samples to aid in the diagnosis, treatment, and monitoring of diseases. This role involves operating and maintaining sophisticated laboratory instruments, ensuring quality and accuracy of test results, and collaborating with healthcare professionals to provide critical diagnostic data. The position requires a deep understanding of clinical biochemistry, laboratory quality systems, and regulatory standards. Key Responsibilities: Conduct biochemical tests on blood, urine, and other body fluids to assess organ function, metabolic conditions, and disease markers. Operate, calibrate, and maintain clin...

Role & responsibilities 3 to 10 years of experience in IT solution or product sales within the healthcare/life sciences domain . Proven track record in selling LIMS, EBPR, or healthcare software solutions . Strong understanding of lab workflows, regulatory processes, and digital healthcare systems . Excellent communication, presentation, and negotiation skills. Ability to work independently and achieve sales targets.

Job description Medispec is seeking a Field Application Scientist (FAS) to provide expert-level training, support, and application optimization for our advanced range of instruments, including Surface Plasmon Resonance (SPR), Flow Cytometers, Seahorse XF Analyzers, Imaging & Multimode Microplate Readers (MMR), and iCIEF systems. This role is ideal for professionals who are passionate about cutting-edge scientific instrumentation, problem-solving, and working closely with researchers, scientists, and sales teams to drive innovation in research and diagnostics. Role and Responsibilities Conduct on-site training and optimization for end-users and the sales team on advanced scientific instrument...

Job Title: EDP Executive Location: Goregaon East Department: IT / Operations Position Type: Full-time Industry Type: biotechnology, life sciences, We are seeking a detail-oriented and proactive EDP Executive to manage and support the organization’s enterprise software systems and electronic data processes. The ideal candidate will be responsible for maintaining software applications, ensuring data accuracy, providing user support and training, and coordinating with internal teams and vendors for system updates and improvements. Key Responsibilities: Manage and maintain the organization’s enterprise software platform and its modules. Provide first-level support and troubleshooting for softwar...

About Sun Pharma: Sun Pharmaceutical Industries Ltd. (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the world with global revenues of US$ 5.4 billion. Supported by 43 manufacturing facilities, we provide high-quality, affordable medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe. Job Summary LIMS Testing & Documentation Specialist will be responsible for the thorough testing of LIMS application before deployment or patch deployment. This role requires a deep understanding of laboratory workflows, strong technical & testing skills, and the ability to work closely with cross-functional teams to ensure the LIM...

About Sun Pharma: Sun Pharmaceutical Industries Ltd. (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the world with global revenues of US$ 5.4 billion. Supported by 43 manufacturing facilities, we provide high-quality, affordable medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe. Job Summary Integration Specialist – LIMS, will be responsible for the integrating various lab instruments/software with LIMS application for successfully establishing paperless environment in QC/R&D Labs. This role requires a deep understanding of laboratory workflows, Instrument connectivity techniques, strong technical skills, a...

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future-ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out www.careers.indegene.com Looking to jump-start your career? We understand how important the first few years of your career are, which create the foundation of your entire professional journey. At Indegene, we promise yo...

Sample preparation Mixing and testing for SBB Plastics Lab for QA, Technical Service, Quality Complaints and New Product Development. Summarize data and test results and enter into LIMS; generate and maintain laboratory documents to ensure prompt and high-quality service to test requestor. Generate and ensure accuracy in precision in testing data of SBB Plastics lab. Maintain all SBB Plastics laboratory instrumentation in a good working order. Key Result Area Safely execute routine analyses via prescribed laboratory procedures to generate reliable and accurate lab results and report the same. Safely perform mixing and testing on samples as per the requested test plan within requested complet...

Ensure quality standards for all products and manufacturing activities. To ensure the GMP compliance throughout the facility. To organize, educate for and execute activity as per the norms of Quality Assurance objective. Handling of customer audits. Releasing or rejecting APIs and Intermediates. Releasing or rejecting intermediates for use outside the control of manufacturing company. Ensure that the work force is highly motivated and aligned to the Company objectives Handling of OOS investigation as per the current requirement. To ensure the compliance of QMS/GMP/GLP Handling of Regulatory audit and compliance (USFDA /EU /TGA /WHO /Cofepress / KFDA) Knowledge, Investigation, CAPA ,Handling ...

Summary The eCompliance Manager is responsible for providing Quality Assurance oversight and guidance with regard to computerized systems validation (CSV), operating within the framework of regulations (GxP, 21CFR11, etc.) and requirements defined in the Novartis Quality Manual and global procedures. eCompliance Manager provides the needed operational support such as approving the GxP impacted changes, Periodic Review Reports, deviations etc., Provides the guidance to the project and operations team on the CSV related topics and related information. Reviews and/or approves the global Computerized Systems key validation deliverables as a part of the eCompliance support to the GxP projects. Ab...

Hands-on experience on testing tools like HP ALM, Kneat and SNOW - Experience to MES, QMS (Trackwise), Lab solutions i.e. LIMS, Empower CDS, Chromeleon, Business Analytics, Middle wares etc. will be an advantage - OT System Qualification (Radio ligand Therapy or critical dosage forms will be a plus) - PAS/DCS Qualification - ISA95 High level of understanding - OT Security will be a plus. - Standalone Systems Qualifications - PAS/DCS Integrated with Manufacturing Equipment qualification. Key components of the responsibilities are as mentioned below but not limited to:  6+ yrs. of Professional experience and strong knowledge with real time experience in IT Quality & Compliance, Computer Syste...

Description About InspireXT : InspireXT is on a mission to build the most trusted supply chains in the world. Our Connected Intelligence vision combines Databricks with deep Oracle ERP/SCM, Salesforce, and industry accelerators to deliver compliant, AI-driven outcomes in Pharma, Manufacturing and Retail. We are investing significantly in our Databricks alliance and building a certified practice from Pune to support global clients across UK, Europe, US and Asia. Role Description As a Databricks Solution Architect at InspireXT, you will partner with our customers to design scalable, governed data architectures and lead migrations into the Databricks Lakehouse. You will bring technical depth an...

Job Description Required Skills: Asset Management, Benefits Management, Cell-Based Assays, Digital Business Development, Digital Technology, Digital Transformation, GMP Compliance, Management System Development, Product Configuration, Product Lifecycle, Product Management, Quality Assurance Processes, Quality Standards, Requirements Management, ROI Management, Stakeholder Relationship Management, Standards Compliance, Strategic Planning, System Designs Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE Secondary Language(s) Job Description: Associate Director - Digital Methods and Data The Opportunity Based in Hyderabad, join a global healthcare biopharma co...

Apply now » Assoc Dir Global Quality Function - 3544 Date: Oct 22, 2025 Location: Bangalore, India, 560064 Company: Teva Pharmaceuticals Job Id: 64643 Who we are Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines e...

Kenvue is currently recruiting for a: APAC Quality Excellence Director What we do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means...

About the job: Represent master data (MD) business operations at the leadership level (M&S Master Data Office lead) and liaise with relevant stakeholders, especially Data & Process Manager at site level and global master data teams. Secure master data (MD) quality and availability at the Sanofi target. Manage master data hub teams. Identify any master data quality and availability issues and propose solutions and remediation (continuous improvement spirit). Main Responsibilities: Partnering with M&S Master Data Office lead and team Guarantee hub activities at the target of quality and responsiveness Managing Master Data team of the hub Put in place effective hub management mechanism: To moti...

Utility Operator HVAC / Water / Electrical (01 Position) based in Vapi, Gujarat. The ideal candidate brings 5 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvemen...

The ideal candidate brings 15-20 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Plan resources, ensure statutory compliance, drive traini...

The ideal candidate brings 5 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen) Own production execution and shift supervision; ensure line clea...

The ideal candidate brings 3- 8 Years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Own production execution and shift supervision; ensure lin...