2502 Lims Jobs - Page 7

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...

Job Title: Senior Trainer Computerized System Validation (CSV) & Data Integrity (ALCOA Principles) Location: Remote Job type: Part-time Job Summary: We are seeking a highly experienced CSV & Data Integrity Trainer with a strong background in regulatory compliance and hands-on experience in validating computerized systems used in GxP environments. The ideal candidate should have in-depth knowledge of GAMP 5, 21 CFR Part 11, EU Annex 11, and ALCOA+ principles , and be capable of delivering engaging, practical training to QA, QC, Manufacturing, and IT professionals. Key Responsibilities: Develop, design, and deliver training programs on Computerized System Validation (CSV) and Data Integrity (A...

Job Responsibilities: 1. Review of Analytical Method Validations/ Verifications protocol/ reports 2. Review of Analytical Method Transfer protocol/ reports 3. Review & release of Reference standard characterization data 4. Review of R&D data and Lab note book for regulatory submission 5. Review of Instrument/Equipment Qualification & Calibration reports 6. Review of CSV (Software Qualification) documents (Protocol &Reports) 7. Review of DS & DP STPs (Reference standard, Raw Material, Intermediate, In process, Semi finished & Finished product). 8. Preparation, Review & training of CQA SOP (Related to R&D Labs) 9. Review of SOPs for R & D function (Analytical Research Laboratory, DDRL (Pilot L...

1. Sampling of raw material, packing material, intermediates, APIs as per approved sampling plan. 2. Carry out analysis of raw material, finished product and packing material as per approved specifications & Method of analysis. 3. Preparation and maintenance of volumetric solutions, reagents, buffers and chemicals. 4. Perform Calibration of QC Instruments and maintain records. 5. Preparation of analytical method transfer and analytical method validation protocols. 6. Perform Analytical method transfer/Analytical Method validation related activities. 7. Prepare Standard operating procedures and to train concerned staff. 8. Preparation of Analytical Protocols, Specification and Method of analy...

Job Title: Executive Business Unit: R&D1 Regulatory Affairs Job Grade G12A Location : Baroda At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” JOB Description: - Method development & Validation by using sophisticated...

Job Title: QC RM (Quality Control – Raw Material) Analyst Location: [Rai, Sonipat] Department: Quality Control (QC) Reports To: QC Manager / QC Head Job Summary: The QC RM Analyst is responsible for testing and analyzing raw materials received from suppliers to ensure compliance with predefined quality specifications. This role is crucial in maintaining product safety, efficacy, and regulatory compliance for third-party manufacturing operations. Key Responsibilities: Conduct routine and non-routine testing of incoming raw materials as per SOPs. Perform physical, chemical, and microbiological tests to verify material quality. Ensure identification, purity, and conformity of raw materials to s...

Position: Lab Manager (Diagnostics Industry) Location : Panchkula Department: Laboratory Operations Reporting To : Medical Director / Operations Head / CEO Key Responsibilities Operational Management Oversee day-to-day operations of the pathology / diagnostic laboratory. Ensure timely and accurate reporting of test results in line with NABL / CAP / ISO standards. Monitor sample collection, accessioning, testing, and reporting workflow to maintain TAT (Turnaround Time). Maintain inventory of reagents, consumables, and instruments to avoid stockouts. Coordinate with sales team to support new B2B tie-ups (clinics, hospitals, labs). Quality & Compliance Implement and monitor internal quality con...

Experience: 1–2 years in QC testing of cosmetics / personal care / FMCG/ pharma. Key Responsibilities 1. Laboratory Testing & Operations Conduct routine and non-routine QC tests on finished goods, raw materials, and packaging (e.g., physical, chemical, microbiological, and stability testing). Operate and maintain QC instruments such as viscometers, rheometers, pH meters, stability chambers, and microbial testing setups. Ensure proper sample handling, preparation, and traceability. Follow SOPs, GLP, and safety protocols during all lab activities. 2. Data Recording & Analytics Accurately document all test results in lab notebooks, LIMS/ERP, or QC databases. Analyze data trends across batches, ...

A. Job Description Interface with customers to understand user business processes and gather their functional requirements needed to configure and customize their new Laboratory Information Management Systems (LIMS). Document system processes and procedures for customer requirements and functionality needs. Working either independently or with other members of the Professional Services team, to analyze and resolve technical project issues, surrounding functional and design requirements. B. Primary Job Objectives Gather, develop, and document functional business requirements for customer projects. Transform the users requirements into functional requirements leveraging both the Sapphire archi...

Company Description We at Entiovi Technologies provide digital transformation using new-age intelligent technologies for more than 8 years. We have clients located primarily in the US and Europe that are served by our dedicated teams. This job is part of our expansion in India. Role Description We are looking for an experienced professional to join our team: Objective: Design and implement a federated Data Mesh architecture for Research Informatics, ensuring “AI-ready” scientific data through standardized Core Data Entities (CDEs), data product governance, and seamless interoperability across domains. Key Responsibilities: Architect the end-to-end data mesh platform using AWS, Snowflake, Pal...

Job Title Executive Business Unit R&D1 Regulatory Affairs Job Grade G12A Location : Baroda At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” JOB Description: - Method development & Validation by using sophisticated i...

Company Description Classic Instrumentation Pvt. Ltd. is a consumer services company based in Noida, Uttar Pradesh, India. We are committed to delivering high-quality testing and research services to our clients, ensuring reliability and accuracy. Our state-of-the-art facilities and experienced team are dedicated to meeting the diverse needs of our clientele. Located in the prominent C-45, Sector 65 area, we strive to set industry standards through our innovative services. Role Description: Test Engineer – Lights & Luminaires The Test Engineer will be responsible for conducting performance, safety, and reliability testing of lighting products and luminaires as per BIS requirements and releva...

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...

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...

Responsibilities: * Drive end-to-end enterprise sales in pharma/life sciences. * Own lead generation, client pitching, pilot-to-deal conversion, and multi-site expansion. * Ideal for those with LIMS, QMS, or compliance software sales experience. Health insurance Sales incentives Performance bonus

Position: HR Recruiter Location: Baner, Pune Experience: 1-3 Years Industry: IT (Healthcare Product) Work Mode - Work From Office Interview Process - Face to Face Roles And Responsibilities Source, screen, and shortlist candidates from job portals, networking sites, referrals, and other sourcing channels. Identify and engage candidates whose skills and experience align with job descriptions and organisational needs. Utilise effective keyword strategies to enhance resume search efficiency. Comprehend job requirements and specifications to ensure accurate candidate matching. Assess candidates' technical skills, relevant technologies, and key responsibilities. Coordinate and schedule telephonic...

Primary skills:Technology->Life Sciences->LIMS A day in the life of an Infoscion As part of the Infosys consulting team, your primary role would be to get to the heart of customer issues, diagnose problem areas, design innovative solutions and facilitate deployment resulting in client delight. You will develop a proposal by owning parts of the proposal document and by giving inputs in solution design based on areas of expertise. You will plan the activities of configuration, configure the product as per the design, conduct conference room pilots and will assist in resolving any queries related to requirements and solution design You will conduct solution/product demonstrations, POC/Proof of ...

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...

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...

Summary Ensure implementation of the e-Compliance strategy and all applicable Novartis and regulatory requirements for all GxP regulated computerized systems and associated infrastructure. Provide oversight, and guidance in the development and implementation of Novartis GxP computerized Systems and processes, including on-going implementation of Data Integrity technical controls within IT systems landscape. Closely cooperate with functional IT staff in the compliant development and delivery of computerized systems to meet GxP requirements. Review and approve CSV deliverables for all Global GxP relevant systems including determination of GxP applicability. About the Role Key Responsibilities:...

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...

Job Title: Sr Executive Analytical Development (AD) Location: Ambernath, India Job Type: Full Time Reporting: Head of Research & Development About Polypeptide Group: PolyPeptide Group AG and its consolidated subsidiaries (?PolyPeptide?) is a specialized Contract Development & Manufacturing Organization (CDMO) for peptideand oligonucleotide-based active pharmaceutical ingredients By supporting its customers mainly in pharma and biotech, it contributes to the health of millions of patients across the world PolyPeptide serves a fast-growing market, offering products and services from pre-clinical to commercial stages Its broad portfolio reflects the opportunities in drug therapies across areas ...

Primary skills:Technology->Life Sciences->LIMS A day in the life of an Infoscion As part of the Infosys consulting team, your primary role would be to get to the heart of customer issues, diagnose problem areas, design innovative solutions and facilitate deployment resulting in client delight. You will develop a proposal by owning parts of the proposal document and by giving inputs in solution design based on areas of expertise. You will plan the activities of configuration, configure the product as per the design, conduct conference room pilots and will assist in resolving any queries related to requirements and solution design You will conduct solution/product demonstrations, POC/Proof of ...

Senior Executive – Power BI (Pharma Industry) Location: Sector-03 Rohini| Department: IT / Business Analytics We are seeking an experienced Senior Executive – Power BI to lead our data analytics and visualization initiatives in the pharmaceutical domain. The ideal candidate will design, develop, and maintain Power BI dashboards and reports to support Sales, Marketing, Supply Chain, and Finance, while ensuring compliance with pharma regulations. Key Responsibilities Lead development of Power BI dashboards & reports for business-critical insights. Integrate data from ERP, CRM, LIMS, Clinical & Regulatory systems . Collaborate with stakeholders to identify needs and deliver actionable analytics...

Job Title : Laboratory Specialist Location : [Saudi Arabia, Hafer Albatin City] Key Responsibilities : Conduct physical, chemical, and mechanical testing of raw materials and finished products (e.g., transparency, inner/outer diameter, tensile strength, burst pressure, flow rate, thermal resistance). Operate and maintain lab equipment such as Vernier calipers, tensile testers, flow meters, FTIR, microscopes, etc. Document and analyze test results according to quality management systems (QMS) and Good Manufacturing Practices (GMP). Assist in product validation and verification activities. Participate in non-conformance investigations and provide technical insights. Ensure compliance with inte...