488 Lims Jobs - Page 16

DiscoveryOne Overview Integrated Drug Discovery, DiscoveryOne, brings together the breadth of functional expertise across the entire Eurofins Discovery organization and combines a wealth experienced drug discovery and program management expertise to design, implement and deliver from idea to IND enabled on behalf of the client. In combining all the chemistry, biology, ADME, pharmacology, safety and toxicology capabilities of Eurofins Discovery, and using our extensive drug discovery expertise and experience, as well as exceptional program management services, DiscoveryOne brings high value, complementary consultative support to enable the client. The virtual project team of Scientific Project Leads and Program Managers, drives the project internally and externally to a successful conclusion and hopefully project renewal. The Project Coordinator/Manager would oversee and coordinate chemistry-focused projects managed by DiscoveryOne but executed at Eurofins Advinus. This role will also support Program Managers in the planning, execution, and assessment of different programs within DiscoveryOne. The Project Coordinator will facilitate effective communication and collaboration across multiple sites and ensure that projects are delivered on time, within scope, and in compliance with contractual requirements. They will also collaborate closely with Program managers, Scientific Project Leads, Client Services teams, Laboratory Operations teams, and other personnel to ensure that the goals, objectives, and outcomes of the program are achieved. Additionally, they will interact with internal and external stakeholders to offer information, feedback, and support. Essential Duties and Responsibilities Project Coordination: Oversee and manage the day-to-day activities of Chemistry-focused projects, ensuring smooth execution and timely delivery Act as the primary point of contact between the different teams and sites involved in the project Ensure seamless coordination between DiscoveryOne, and the Chemistry teams across different sites Review and verify contractual requirements to ensure they are being met Work with legal and finance teams to ensure compliance with contract terms, deliverables, and payment schedules Monitor project progress and ensure deadlines are met Maintain and update program databases and records Collaboration and Support to DiscoveryOne Program Management team (Study Coordination): Provide administrative support to program managers Assist in the development and execution of program strategies and activities Responsible for processing orders from clients and organizing materials for project implementation, from quote and sales order generation to study completion Facilitate communication between program managers and internal client services and operations teams, keeping program managers informed of study status, turnaround times and delays or potential issues and operations teams informed of client requirements Initiate and track studies under DiscoveryOne, ensuring timely study activation and data delivery Maintain and update program databases and records Monitor study/project progress and ensure deadlines are met Perform other duties as assigned Qualifications/ Requirements: Education Associate’s or Bachelor’s degree in Chemistry or equivalent; or more than 3 years related experience and/or training in project management; or equivalent combination of education and experience. Proven project management ability, with excellent follow-up and close-out skills Experienced in writing and interpreting documents such as standard operating procedures, instructions, and contracts and agreements with demonstrated attention to detail Knowledge of integrated drug discovery process and bringing drugs to market in Pharma or Biotech is preferred Experience in Microsoft Dynamics AX Software and Laboratory Information Management System (LIMS) is preferred Preferably from the CRO industry Strong organizational and time management skills Excellent written and verbal communication Ability to work independently and in a team environment Coordinate with team members from different regions to meet deadlines and program milestones Demonstrate adaptability in accommodating flexible working hours to support a seamless collaboration environment Detail-oriented with strong problem-solving abilities Mentality/ Skills Strong organizational and time management skills Excellent written and verbal communication Ability to work independently and in a team environment Coordinate with team members from different regions to meet deadlines and program milestones Demonstrate adaptability in accommodating flexible working hours to support a seamless collaboration environment Detail-oriented with strong problem-solving abilities Show more Show less

• Creation and revision of Master documents: Specification, Standard Operating Procedure and General Procedures. • Implementation of Pharmacopeial Updates and Source Change Document. • Managing master data operations within the LIMS and SAP system.

About the Role We are seeking a dynamic Sales Professional with experience in industrial tools or lubricant services to join our team in Jamshedpur. This role combines technical service with sales and customer support. You'll work closely with our clients, understand their needs, and support them through product demos, technical consultations, and service activities.  Position: Sales Professional – Industrial Tools / Lubricant Accessories or Services (3 - 7 Years ) Location: Jamshedpur, Jharkhand Industry: Lubrication accessories or services or Industrial Tools Experience : 3 - 7 Years Role Type: Work From Office (Includes Travelling) Key Responsibilities Lead generation, pre-sales activities, and follow-ups. Prepare proposals, close deals, and manage post-sales engagement. Provide technical support for product demos and application guidance. Install, calibrate, and service instruments used in lubricant condition monitoring (e.g., FTIR, viscometers, particle counters, spectrometers). Train customers on instrument operation and basic maintenance. Troubleshoot issues on-site or remotely; maintain detailed service records. Build and maintain strong customer relationships; relay technical feedback to internal teams. Requirements Minimum 3 years of experience in B2B sales of industrial tools, lubricant accessories, or related services. Strong technical knowledge of lubrication systems, tools, or related equipment. Background in Mechanical, Instrumentation, or Chemical Engineering. Excellent communication and customer-facing skills. Willingness to travel for installations, service visits, and sales support. Preferred Qualifications Experience with brands like Spectro Scientific, Tanaka, Anton Paar, etc. Exposure to ISO 17025 labs, reliability, or maintenance programs. Familiarity with LIMS systems and laboratory quality standards. Education Bachelor's Degree in Engineering (Mechanical / Chemical / Instrumentation or related field). Interested candidates can send their resume to: puja.agarwal@tribologysolutions.com Contact: 9708600011 Join us in delivering precision and performance through cutting-edge lubrication solutions! Show more Show less

We are seeking an experienced and passionate Remote Quality Control (QC) Trainer to join our team. This role is ideal for professionals with extensive hands-on experience in GMP-compliant laboratory environments and expertise in analytical instrumentation. If you thrive in a training role and want to empower the next generation of pharmaceutical professionals, we’d love to hear from you. Key Responsibilities Deliver live, online training sessions covering: Good Manufacturing Practices (GMP) Analytical techniques: HPLC, UV-Vis, FTIR, GC, and titration Train participants in: Instrument calibration, maintenance, and troubleshooting Practical usage of LIMS and Empower software Design and develop clear, engaging training content and materials Support trainees with personalized guidance and practical insights Qualifications Bachelor’s degree (or higher) in Pharmacy, Chemistry, or a related field Minimum 5 years of QC experience in the pharmaceutical industry In-depth knowledge of GMP regulations and compliance practices Proficient with laboratory instruments and software tools used in QC labs Exceptional communication and presentation skills Proven ability to train and engage remote learners effectively Compensation & Benefits Competitive pay per training session Performance-based incentives tied to successful candidate placements Flexible scheduling to suit your availability 100% remote – train from anywhere Show more Show less

I’m helping Confident LIMS find a top candidate to join their team as an SQL Data Analyst with a flexible type of job. This is a cool job because you will build cutting edge data models and dashboards to power labs worldwide with precision and impact. Compensation: USD 20K - 50K/year. Location: Remote (anywhere). Mission of Confident LIMS: "Empower analytical labs to thrive by making complex workflows simple, seamless, and client focused.” What makes you a strong candidate: You are expert in data analytics, PostgreSQL, and SQL. You are proficient in AWS, cloud computing, and Metabase. English - Conversational. Responsibilities and more: Requirements: 3+ years of experience as data analyst/data scientist using SQL. Expert in building high performance and efficient SQL queries and data models in Metabase. Excellent attention to detail, consistently produces high-quality work delivered on time. Comfortable working independently and asynchronously on remote team to meet deadlines with minimal management oversight. Conversational in written English. General responsibilities: Lead and execute the development of various data models, databases and data analytics dashboards to be made available to the end users of Client’s customers within Client’s software application and selected third-parties outside of Client’s software application using Client’s current technology infrastructure (AWS, PostgreSQL, Metabase, and React). Scope of work outline: - Build new “Simplified Models” (or tables, TBD) to query using Metabase. - Build new Basic and Pro plan data analytics dashboards in Metabase querying the new Simplified Models for only the authenticated customers’ data: a. For Labs: Starter / Basic Plan (approximately 5-10 queries). Pro Plan (approximately 10-20 queries). b. For Clients: Basic Plan (approximately 5-10 queries). Pro Plan (approximately 10-20 queries). - Build new “Public Database” with aggregated and anonymized data from the new simplified models for use in new Premium Plan Metabase queries and to be made available to select third-party researchers on a case-by-case basis. - Build new Premium plan data analytics dashboards in Metabase joining specific customers’ data from the new Simplified Models and the new Public Database that allows authenticated users to join and concurrently display their organization’s data from the Simplified Models with the “benchmark data” from the Public Database (approximately 10-20 queries). Show more Show less

Job Description – Executive - Tablet Packaging Job Title: Executive – Tablet Packaging Location: Indore – Regulated Pharma Manufacturing Plant Department: Production – Packaging (OSD) Reporting To: Manager / Sr. Manager – Packaging Job Type: Full-Time | Executive Level Job Purpose To execute primary and secondary packaging of tablets in compliance with packaging plans, cGMP, and regulatory requirements while maintaining quality and efficiency. Key Responsibilities Execute blister / alu-alu / strip / bottle packaging as per approved Batch Packaging Records (BPR). Operate packaging line equipment like blister pack machines, cartonators, inkjet/online printers, deblistering machines . Carry out line clearance in coordination with QA. Perform in-process checks: batch coding, leaflet insertion, sealing, pack integrity, and labeling . Maintain cleanliness and hygiene of the packaging area and equipment. Ensure proper usage and accountability of packaging material (PM). Record entries in logbooks, BPRs, and online systems (LIMS/SAP). Adhere to data integrity, safety norms , and regulatory compliance requirements. Skills & Competencies Knowledge of primary and secondary packaging processes and equipment. Understanding of SOPs, GMP , and packaging documentation requirements. Good coordination and observation skills. Experience in facing regulatory audits is a plus. Qualifications B.Pharm / M.Pharm / B.Sc. (Science) 2–5 years of experience in regulated pharmaceutical packaging environments. Show more Show less

Summary Manage cost effective GxP Compliance and/or Audit activities, operations and systems to ensure compliance of business areas with the Novartis Quality Manual and Policies and all relevant GxP, legal and regulatory requirements, and through internal audits, KPIs (Key Performance Indicators) and KQIs (Key Quality Indicators) -Performs preparation and management of external and corporate audits and Health Authority inspections. About The Role eCompliance Manager About The Role: 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. Key Responsibilities: Quality oversight of operational activities of GxP systems (e.g., Changes, Periodic Reviews, Deviations etc.,) Provide needed support to meet the applicable Novartis and regulatory requirements for GxP regulated computerized systems projects. Point of Contact for all CSV related matters for GxP Computerized Systems and act as an interface between IT and Business for eCompliance topics in relation to GxP classified Computer Systems promoting a Quality Culture. Review and approve project related documents for GxP relevant systems including determination of GxP applicability for all GxP and non-GxP relevant systems. Establish trusted partnership with assigned IT Function with understanding of business drivers, and provide the needed day to day operational support. Review and approve the GxP Changes and the associated deliverables. Review and approve the GxP impacted deviations, ensure appropriate CAPA are implemented. Contribute for the preparation of VMP and execute the plan for the systems associated with the respective functions. Review and approve the Periodic Review Reports for the GxP computerized systems and the associated gaps within CAPA Management System. Manage GxP supplier qualification activities Provide Audit support as assigned and in case of CAPAs, provide the required Quality support. Essential Requirements: 10-15 years of overall IT experience, and a minimum 7 years of relevant experience in the Pharmaceutical Industry and in particular within regulated functions such as IT Quality and Compliance Solid understanding of global regulations and Health Authorities expectations governing computerized systems (CSV, Part 11, etc.) Solid experience in the development, implementation and lifecycle management of computerized systems in regulated environments Experience in quality management of Cloud, SaaS platform, mobile and digital application used in regulated environments Highly experienced in the operational management of GxP solutions including its related technologies to support the operation Good understanding in system application management, its Quality support approach and industry best practices (ITIL, ITSM, etc.) Experience in the development, implementation and lifecycle management of key computerized systems in the Pharmaceutical Development, Manufacturing, Quality, Commercial and Infrastructure space (e.g. ERP/SAP, MES, LIMS, CRM, IAM, etc.) Desirable Requirements: Degree in Information Technology, Life Sciences, Pharmacy, Engineering or equivalent. Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Show more Show less

Responsibilities: a) Lead and manage a team of IOPS IT support engineers, providing guidance, training, and performance evaluations b) Oversee the support and maintenance of the IOPS IT applications such as Discoverent/SIMCA/LIMS/ BMRAM/ OpsTrakker/ Orchestrate/EconnX, ensuring system availability and performance. Address and resolve technical issues promptly c) Provide advanced technical support to end-users, addressing complex issues and ensuring user satisfaction d) Work closely with IT, laboratory, and quality assurance teams to ensure seamless integration and operation of the LIMS. Collaborate on system upgrades and enhancements e) Ensure compliance with industry regulations and internal quality standards. Maintain comprehensive documentation of system configurations, procedures, and support activities f) Manage system upgrades and process improvements. Coordinate with vendors and external partners as needed g) Monitor system performance and generate reports on key metrics. Identify areas for improvement and implement solutions to enhance system efficiency h) Develop and deliver training programs for end-users and support staff on IOPS IT functionalities and best practices i) Address user queries, service requests, and technical issues through the IT support ticketing system. Skills: a) Strong technical knowledge, excellent leadership and communication skills, problem-solving abilities, and the ability to work collaboratively with cross-functional teams. b) Basic scripting knowledge (PowerShell, Python, or Shell scripting) is a plus. c) Excellent problem-solving and troubleshooting abilities. d) Strong communication and interpersonal skills to support non-technical users. e) Ability to work independently and as part of a cross-functional team. Show more Show less

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Company Overview: At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 39,000 employees around the world work to discover and bring life-changing medicines to those who need them the most, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Tech@Lilly builds and maintains capabilities using cutting edge technologies like most prominent tech companies. What differentiates Tech@Lilly is that we redefine what’s possible through tech to advance our purpose – creating medicines that make life better for people around the world, like data driven drug discovery and connected clinical trials. We hire the best technology professionals from a variety of backgrounds, so they can bring an assortment of knowledge, skills, and diverse thinking to deliver innovative solutions in every area of our business. LRL Tech unites science with technology to accelerate the Research and Development of medicines and to deliver therapeutic innovations. The team leverages technology and platforms to streamline scientific experimentation to help Researchers follow the science, to understand the disease and identify potential therapies. They are at the forefront of advanced analytics to enable data driven drug discovery, to innovate so Scientists can rapidly analyze and accelerate the discovery of new medicines. Position Overview: We are looking for a hands-on, Advisor - Informatics & Scientific Applications Architect to design and deliver next-generation digital platforms supporting drug discovery, preclinical research, analytical sciences, and CMC applications. This role demands deep expertise in AWS serverless architectures, cloud-native designs, automation, and microservices for scientific data applications. You will play a key leadership role in architecting multi-tenant, high-performance, modular, and scalable informatics ecosystems that integrate scientific workflows, computational platforms, and cloud infrastructure. Key Responsibilities: Architectural Leadership: Architect and build a multi-tenant, serverless informatics platform leveraging AWS Lambda, DynamoDB, S3, EBS, EFS, Route 53, and API Gateway. Design data partitioning strategies for multi-tenant scientific data storage and explore microservices frameworks for scalable architecture. Lead cloud-native software design using Kubernetes, Docker, and containerized services, ensuring high reproducibility and scalability of scientific applications. Build scalable Research Data Lakes, asset registries, and metadata catalog to support large-scale scientific data ingestion and retrieval. Complex Scientific Data Flow & Interoperability: Architect frameworks that facilitate seamless data exchange between discovery research systems, including LIMS, ELN, analytical tools, and registration systems. Implement RESTful and GraphQL APIs for high-performance data interoperability across computational models, bioassays, and experimental workflows. Establish scientific data standards to ensure consistency, traceability, and governance across the R&D landscape. Scientific Workflow Automation & Computational Frameworks: Architect scientific workflow automation platforms using Apache Airflow, EventBridge, RabbitMQ, and Kafka, enabling real-time data acquisition and bioassay processing. Design platforms supporting in silico modeling, AI-driven analytics, and high-throughput screening simulations. Integrate Cloud (AWS/Azure) platforms with HPC clusters to handle bioinformatics, cheminformatics, and translational modeling workloads. Cloud, DevOps, and Observability: Maintain deep technical hands-on expertise with AWS CloudFormation, Ansible, Jenkins, Git, and other DevOps automation tools. Implement observability solutions using Prometheus, Grafana, OpenTelemetry to monitor system health, performance, and workflows. Continuously learn, explore, and drive adoption of cutting-edge cloud-native, containerization, serverless, and scientific informatics trends. Cross-Functional Scientific Collaboration: Collaborate closely with scientists, data scientists, computational biologists, formulation teams, and manufacturing engineers to co-create informatics solutions. Serve as a trusted technical advisor for cloud migration, scientific data modernization, and AI/ML integration projects. Work with UI/UX teams to create intuitive digital interfaces for scientific workflow automation and data exploration. Technology Strategy, Governance & Best Practices: Drive architectural strategy, making informed decisions around buy vs. build, third-party integrations, and platform extensibility. Define and enforce best practices for scientific IT security, data privacy, compliance (GxP, FAIR), and cloud operations. Champion a modular, service-oriented, event-driven architecture to enable rapid innovation, maintainability, and scalability. Required Qualifications: Experience: 10+ years of enterprise IT and scientific informatics architecture experience. Deep technical leadership experience in AWS serverless and scientific data integration projects. Proven experience building cloud-native, scalable platforms integrating LIMS, ELN, MES, compound registries, and scientific analysis tools. Education: Bachelor’s or Master’s degree in Computer Science, Bioinformatics, Information Systems, or related disciplines. Technical Expertise: Expertise in AWS serverless architectures (Lambda, DynamoDB, S3, Route53, API Gateway), containerized platforms (Kubernetes, Docker), and scientific workflow tools (Airflow, Kafka, EventBridge). Strong knowledge of microservices design, DevOps automation, scientific data systems, and HPC integration. Experience in observability setup for complex distributed systems in scientific environments. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. #WeAreLilly

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 Roles & Responsibilities To perform In-process and Finished product tests for Assay, Related substance, Residual solvent, UOD, Dissolution, and Water content. To perform Exhibit, Hold time and process validation samples analysis. To Handle HPLC, GC, Dissolution, UV and KF systems and its maintenance. To handle Empower software, sample sets loading and processing independently. Good experience in chromatography. Knowledge on Investigations, Deviations, OOT and OOS. To handle SAP, LIMS and DCMS activities. To follow good laboratory practices (GLP) and good documentation practices (GDP). Qualifications Educational qualification: MSC chemistry, B-Pharm Minimum work experience: 5-7 years years in QC. Show more Show less

A Day in Your Life at MKS: As an LIMS Expert and Laboratory Applications Administrator in IT Business applications team at MKS ATOTECH based in Poznan, you will partner with cross-functional teams including IT, laboratory personnel, and other departments to ensure the success of LIMS implementation and operation as well as providing internal consulting and administration for LIMS (Laboratory Information Management System) and other R&D/Labs related applications (e.g. ELN). In this role, you will report to the Manager SAP SCM & R&D/Labs. This position is on a hybrid mode, 8 days onsite per month. You Will Make an Impact By: Leading the implementation of the new LIMS solution, ensuring alignment with lab operations and business needs. Overseeing the integration of the LIMS system with SAP and other lab-related applications (e.g. ELN) to ensure smooth data flow between the systems, including master data, inventory management, and reporting. Providing ongoing administration and support for the LIMS, ensuring its optimal functionality, reliability, and performance. Provide support for LIMS and other R&D/Labs related applications (e.g. ELN) in cooperation with internal and external support partners. Offering trainings to IT and lab personnel and end-users, and provide troubleshooting and support for system-related issues. Managing other labs-related applications /e.g. ELN, Hull Cell ML), ensuring they are maintained and function effectively alongside the LIMS system and with SAP SCM environment. Identifying opportunities for process improvements and automation within the lab and propose solutions to increase efficiency. Ensuring proper documentation and compliance with regulatory requirements (e.g., GLP, ISO standards) related to LIMS and other lab-related applications. Working closely with cross-functional teams including IT, laboratory personnel, and other departments to ensure the success of LIMS implementation and operation. Building trustful partnership with business stakeholders, support requirements gathering and clarification processes. Performing other related duties that may be assigned or associated with the responsibility of the position. International personality able to support all countries globally. The successful candidate will be responsible for : coordinating implementation, administration, and supporting a new cloud-based Laboratory Information Management System (LIMS) as pilot in Germany and for its rollout to further regions globally, including its integration with SAP and other lab-related applications (e.g. ELN). Taking responsibility for other labs-related applications (e.g. ELN, Hull Cell Machine Learning Application) and ensure they are seamlessly integrated into our systems. Taking responsibility for the LIMS for requirements gathering, clarification and evaluation, solution design, configuration, data migration, data mapping/testing, documentation, training, problem resolution and support. Being co-responsible for initiating, executing, and/or managing Change Requests and Projects with relation to Portfolio Demand Management processes The expected end result is the successful implementation and administration of a cloud-based LIMS including its integration to SAP and ELN, data migration from previous LIMS solution as well as the successful rollout to other regions. Additionally successful delivery of solutions in LIMS and other R&D/Labs related applications (e.g. ELN), offering improvements to users, and excellence in help desk support. Travel Requirements: Up to 25 % of Travel (locally and international) is required. As part of the global team, a certain ability of flexible working hours is expected. Skills You Bring: Bachelor's degree in computer science, Information Systems or related field Min 4-5 years of experience in a similar position, experience in in-house or external consulting. Experience in implementing and administrating LIMS systems, including implementation coordination, configuration, and support. Solid understanding of laboratory processes, data flow, and requirements. Ability to work independently and manage multiple priorities in a fast-paced environment. Strong problem-solving and troubleshooting skills. A proven track record of accomplishments and strong interpersonal skills are required Strong verbal and written English communication skills and ability to work with other global teams' resources are required. Preferred Skills: Experience with specific LIMS platforms (e.g. Labvantage, Thermo Fischer, LabWare, STARLIMS, ). Functional and technical experience in SAP QM and SAP PM modules is a clear plus. Experience in managing ELN and other lab-related applications is useful. Knowledge of data security and data integrity best practices in laboratory environments. We can't wait for your application ! Show more Show less

A Day in Your Life at MKS: As an LIMS Expert and Laboratory Applications Administrator in IT Business applications team at MKS ATOTECH based in Poznan, you will partner with cross-functional teams including IT, laboratory personnel, and other departments to ensure the success of LIMS implementation and operation as well as providing internal consulting and administration for LIMS (Laboratory Information Management System) and other R&D/Labs related applications (e.g. ELN). In this role, you will report to the Manager SAP SCM & R&D/Labs. This position is on a hybrid mode, 8 days onsite per month. You Will Make an Impact By: Leading the implementation of the new LIMS solution, ensuring alignment with lab operations and business needs. Overseeing the integration of the LIMS system with SAP and other lab-related applications (e.g. ELN) to ensure smooth data flow between the systems, including master data, inventory management, and reporting. Providing ongoing administration and support for the LIMS, ensuring its optimal functionality, reliability, and performance. Provide support for LIMS and other R&D/Labs related applications (e.g. ELN) in cooperation with internal and external support partners. Offering trainings to IT and lab personnel and end-users, and provide troubleshooting and support for system-related issues. Managing other labs-related applications /e.g. ELN, Hull Cell ML), ensuring they are maintained and function effectively alongside the LIMS system and with SAP SCM environment. Identifying opportunities for process improvements and automation within the lab and propose solutions to increase efficiency. Ensuring proper documentation and compliance with regulatory requirements (e.g., GLP, ISO standards) related to LIMS and other lab-related applications. Working closely with cross-functional teams including IT, laboratory personnel, and other departments to ensure the success of LIMS implementation and operation. Building trustful partnership with business stakeholders, support requirements gathering and clarification processes. Performing other related duties that may be assigned or associated with the responsibility of the position. International personality able to support all countries globally. The successful candidate will be responsible for : coordinating implementation, administration, and supporting a new cloud-based Laboratory Information Management System (LIMS) as pilot in Germany and for its rollout to further regions globally, including its integration with SAP and other lab-related applications (e.g. ELN). Taking responsibility for other labs-related applications (e.g. ELN, Hull Cell Machine Learning Application) and ensure they are seamlessly integrated into our systems. Taking responsibility for the LIMS for requirements gathering, clarification and evaluation, solution design, configuration, data migration, data mapping/testing, documentation, training, problem resolution and support. Being co-responsible for initiating, executing, and/or managing Change Requests and Projects with relation to Portfolio Demand Management processes The expected end result is the successful implementation and administration of a cloud-based LIMS including its integration to SAP and ELN, data migration from previous LIMS solution as well as the successful rollout to other regions. Additionally successful delivery of solutions in LIMS and other R&D/Labs related applications (e.g. ELN), offering improvements to users, and excellence in help desk support. Travel Requirements: Up to 25 % of Travel (locally and international) is required. As part of the global team, a certain ability of flexible working hours is expected. Skills You Bring: Bachelor's degree in computer science, Information Systems or related field Min 4-5 years of experience in a similar position, experience in in-house or external consulting. Experience in implementing and administrating LIMS systems, including implementation coordination, configuration, and support. Solid understanding of laboratory processes, data flow, and requirements. Ability to work independently and manage multiple priorities in a fast-paced environment. Strong problem-solving and troubleshooting skills. A proven track record of accomplishments and strong interpersonal skills are required Strong verbal and written English communication skills and ability to work with other global teams' resources are required. Preferred Skills: Experience with specific LIMS platforms (e.g. Labvantage, Thermo Fischer, LabWare, STARLIMS, ). Functional and technical experience in SAP QM and SAP PM modules is a clear plus. Experience in managing ELN and other lab-related applications is useful. Knowledge of data security and data integrity best practices in laboratory environments. We can't wait for your application ! Show more Show less

This Senior-level position requires extensive hands-on experience with designing, implementing and overseeing testing solutions as well as the ability to apply these concepts across various technology platforms (web-based, client-server, service oriented, legacy/mainframe, middleware components, etc.). Either the practical experience working with legacy-based applications or the hands on extensive hands-on experience with designing, implementing and overseeing testing solutions as well as the ability to apply these concepts across various technology platforms are necessary to perform in this role. It requires the ability to identify, plan and execute testing activities to ensure high quality software and ensure compliance according to regulatory statues, policies and procedures. In addition, it may also require the ability to utilize middleware components such as IBM’s messaging queues or interfaces to perform validation of an application. Actual testing could consist of testing types such as white-box/black-box, functional, etc. to ensure application functionality. The analyst will create and maintain test plans, cases, test data and summary artifacts as well as execute testing scenarios for verification. The analyst must be able to provide work estimates for testing activities and report on quality statistics and metrics, record and monitor issues until resolution. Individual must promote continuous improvement and strive for methods to improve testing through the use of testing tools. Roles & Responsibilities Bachelor’s degree or foreign equivalent in technical, information systems or clinical/business related field. Clinical Healthcare experience a plus. Five years or more experience as a software quality analyst with experience using software quality tools to facilitate testing or hands-on lab experience with respective lab systems. Ability to follow established processes, SOPs and testing methods throughout the software lifecycle while continuously driving quality into the overall work process. Collaborate with various IT entities such as the Business Analysts, Development, Support, Project Management, etc. as dictated by the task or project deliverable. Ability to use defined business or product requirements documentation to perform the appropriate test validation to ensure the proper implementation of key functionalities. Create and/or review test plans or test summary documentation outlining the test approach and test outcomes of the test execution. Create test cases and scenarios to perform the appropriate test validation based on the defined requirements documents. Provide testing updates and metrics based on the test execution process. Serves as a conduit between the IT entities and the business community (internal or external customers) to ensure alignment on test executions and processes. Organize and manage assigned tasks, provide project estimations and perform risk assessments and planning based on the work assignment. Provide peer support, Production support during normal or off-hour timeframes. Self-managing with the ability to control the analysis and quality processes throughout the software lifecycle while continuously driving quality into the overall work process. Ability to analyze complex processes and develop logical conclusions and approach in order to implement effective solutions Bachelor's degree or equivalent experience in a technical, business, or clinical discipline Understanding of software testing methodologies, use of software tools for artifact creation and management and different testing types Must be able to work independently in the absence of supervision Laboratory experience working with LIMS systems a major plus but not required. Experience in functional testing of web-based applications Analyzing software requirements and preparing test scenarios. Experience in selenium with Java. Experience in BDD framework Experience in testing Web APIs including REST, xml based using tools like Postman, SOAP UI, REST Assured etc. Interacting with clients to understand product requirements. Participating in design reviews and providing input on requirements, product design, and potential problems. Worked in Waterfall or Agile methodologies Should have strong exposure to web-based application testing and related tools Good Communication Skills, written & speaking. Proficient in creating and executing SQL queries Familiarity with tools such as Git, ALM/Jira/Bugzilla, Rally Experience in creating automation framework from scratch Sound knowledge of creating documentations/artifacts related to testing Knowledge in deployment of Java based applications Awareness of QA metrics like rejection ratio, defect leakage, pass rate etc. Experience 4- 7 years of experience required Labcorp Is Proud To Be An Equal Opportunity Employer Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement. 256966 Show more Show less

Summary Novartis operates multiple manufacturing sites globally to produce cutting-edge Cell and Gene Therapy products and Biologics (Large Molecules). As a Discoverant Specialist, you will play a pivotal role in supporting the Discoverant System Business Owner within Novartis Technical Operations (NTO). Discoverant is a validated IT solution utilized across NTO for automated manufacturing data aggregation, advanced analysis, and comprehensive reporting. In this role, you will act as the global Discoverant Super User, collaborating with IT teams, manufacturing sites, and the Discoverant Global Business Owner. Your responsibilities will include ensuring optimal system setup, seamless change implementations, and ongoing maintenance of the Discoverant platform across the Novartis network. About The Role Major Accountabilities Serve as the primary business-side representative for the implementation, lifecycle management, and ongoing evolution of the Discoverant system, ensuring effective collaboration with local users, IT, and system vendors under the guidance of the business owner. Coordinate Discoverant interfaces with integrated IT systems, including ERP (SAP), MES, LIMS, Data Historians, and patient scheduling tools (e.g., CellChain), leveraging cloud-based manufacturing and quality data storage solutions. Facilitate onboarding for new internal and external users, conduct training sessions, and promote knowledge sharing among end users. Develop and optimize data analytics components, including dashboards, control charts, automated reports, and advanced analytics, utilizing best practices and tools like Pipeline Pilot. Drive change control processes for the Discoverant system, integrating new parameters, products, and architectural updates, including respective interface modifications, while supporting local and global risk and impact assessments. Support data integration from new systems and parameters into Discoverant to meet manufacturing data trending and analysis needs, aligning data flow from source systems to Discoverant and advanced analytics platforms. Assess data quality, implement corrective actions, and propose improvements to ensure data accuracy and reliability. Manage manufacturing data provision for internal stakeholders outside the manufacturing group. Address and resolve Discoverant-related deviations, quality events, and associated actions. Act as a liaison between local Discoverant users, IT teams, and system vendors to ensure smooth operations and system enhancements. Author and maintain Discoverant-specific Standard Operating Procedures (SOPs) and Working Procedures (WPs). Key Performance Indicators (Indicate how performance for this role will be measured) Quality / Accuracy / Right First Time Timeliness Deviations / Escalations Job Dimensions ( Number of staff reporting) Indicate key facts and figures) Direct: 0 Financial responsibility (Budget, Cost, Sales, etc.) Operational Budget: na Impact on the Organization Contribute to increased level of automation in manufacturing Significant impact on ensuring competitive advantage in quality and costs by improving the relevant data and digital technology standards Contribute to Site Manufacturing financial / business goals. Minimize process-related rejected batches and write-offs. Maximize process robustness Skills Good Documentation Practice Effective communicator Strong cross functional collaboration Adaptability to Embrace Change Effective stakeholder engagement Manufacturing Process Knowledge Of GMP (Good Manufacturing Practices) Change Control Deviation management Corrective and preventive action (CAPA) Continual Improvement Process General HSE Knowledge Manufacturing (Production) Education (minimum) Ideal Background / Requirements for the role University degree in Engineering, Computer Sciences, Technology (Chemical/Biology) or similar field Languages Fluent in English and additional languages desirable (German, French, other) Relevant Experiences 5 years of practical experience in the pharmaceutical industry, with expertise in manufacturing IT systems. Hands-on experience with Biovia's Discoverant and Pipeline Pilot tools. Knowledge of integrated IT systems such as ERP (SAP), MES, LIMS, OSI-PI, SQL, Oracle/MS SQL databases, and cloud-based data storage solutions. Comprehensive understanding of pharmaceutical cGMP, Computerized System Validation (CSV), and regulatory requirements. Familiarity with statistical tools and programming languages such as Minitab, JMP, Python, and R is a plus. Knowledge of data handling applied statistics, and Six Sigma methodologies. Proven ability to collaborate effectively with team members, site experts, and organizational leaders, with a capacity to influence without direct authority. Solid project management and presentation skills, with the ability to lead cross-functional initiatives. Excellent communication and interpersonal skills to foster collaboration and drive results. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Show more Show less

Job Summary We are seeking a Sr. Business Analyst with 4 to 6 years of experience to join our team. The ideal candidate will have expertise in Labware and any LIMS with a strong domain knowledge in LIMS - Labware and LabVantage. This hybrid role offers the opportunity to work in a dynamic environment contributing to the success of our projects and the betterment of society. Responsibilities Analyze and document business requirements for LIMS projects Collaborate with stakeholders to gather and validate requirements Provide expertise in Labware and other LIMS systems to ensure project success Develop functional specifications and system design documents Oversee the implementation of LIMS solutions ensuring alignment with business needs Conduct system testing and validation to ensure quality and compliance Provide training and support to end-users on LIMS functionalities Troubleshoot and resolve issues related to LIMS systems Ensure data integrity and security within LIMS applications Collaborate with cross-functional teams to achieve project goals Monitor project progress and report on key metrics Identify opportunities for process improvements and recommend solutions Stay updated with industry trends and best practices in LIMS. Qualifications Must have experience with Labware and any LIMS Strong domain knowledge in LIMS Labware and LabVantage Excellent analytical and problem-solving skills Ability to work collaboratively in a hybrid work model Strong communication and interpersonal skills Experience in system testing and validation Show more Show less

Roles & Responsibilities 1. To perform In-process and Finished product tests for Assay, Related substance, Residual solvent, UOD, Dissolution, and Water content. 2. To perform Exhibit, Hold time and process validation samples analysis. 3. To Handle HPLC, GC, Dissolution, UV and KF systems and its maintenance. 4. To handle Empower software, sample sets loading and processing independently. 5. Good experience in chromatography. 6. Knowledge on Investigations, Deviations, OOT and OOS. 7. To handle SAP, LIMS and DCMS activities. 8. To follow good laboratory practices (GLP) and good documentation practices (GDP). Qualification Educational qualification: MSC chemistry, B-Pharm Minimum work experience: 5-7 years years in QC. Additional Information

Job description Candidate will be based at corporate office of reputed Pharma company as a Manager- IT and he will be responsible for handling following:- Job Responsibilities: 1 Candidate would be responsible for the Servers and Computers, Printer and accessories are working properly any given time. 2) The Master Creation in the SAP Batch master is to be done properly. Backup of Servers and Computers are done from time to time. And functions of all camera system installed at plant to ensure proper support to the users.to prepare Presentation, SOPs and participate etc. for the IT compliance training. 3) He have good knowledge of administer LAN, WAN, EPABX & Video Conferencing. 4) Candidate would be responsible Daily Monitoring of all IT compliance with respect to Quality Assurance activities. IT compliance and data integrity Training to IT Team Members. Creation and Review of Qualification/ Validation related documents. Review of IT Training Matrix and Internal Trainer list. 5) Candidate would be responsible impart GSP, GLP, Behavioural, Motivational and other kind of trainings (Classroom & QC), ensuring compliance of the specified procedures / guidance and review of qualification documents such as URS, DQ, IQ, OQ, PQ and validation protocols and validation study report. 6) Candidate would be responsible for various Regulatory and Customer audits and assist management in providing compliance to audit observations and to review performance of juniors and recommend for higher punishment in case of their indulgence in any kind of misconduct including any data integrity. 7) Candidate would be responsible implementation and operation of Document Management (DMS), Quality Management System (QMS), Training/Learning management system (LMS), Lab Info. Management (LIMS) Software. 8) Candidate would be responsible troubleshooting any issues in SAP and subsequent validation and documentation of any modifications, enhancement or upgrades in any and all softwares implemented in the facility. 7) Candidate will be responsible for monitoring the performance of factory network, conduct regular internal audits and implement necessary modifications or adjustments to optimize resources.and CSV Activities with GAMP5 Approach with a yearly planner. And define and manage IT Disaster recovery strategy and Compliance and security for all IT related systems and infrastructure. Required candidate profile Qualification- Bachelors degree in Computer Science, Computer Application. . Candidate should have 8 to 12 yrs. in relevant experience in Hardware & Software. Candidate should have good experience in SAP, of Document Management (DMS), Quality Management System (QMS), Training/Learning management system (LMS). Candidate should have good Knowledge of LAN, WAN, EPABXETS. Should have good Knowledge of Daily Monitoring of All IT Compliance

Job Summary We are seeking an associate for the Quality team responsible for conducting sampling and analysis of packaging and raw material samples. The role involves ensuring accuracy in documentation, adherence to safety procedures, reporting discrepancies, and maintaining lab safety. Roles & Responsibilities • You will be responsible for conducting sampling and analysis of raw material samples as allotted by the group leader. • You will also be responsible for the proper use and care of instruments or equipment as instructed in relevant SOPs (Standard Operating Procedure), including cleaning before and after analysis. • You will adhere to safety precautions and procedures during analysis. • Your responsibilities include placing SOP/STP/reference standards at their designated locations after analysis, and reporting discrepancies or incidents promptly to the Group Leader. • Lab safety, following JSA (Job Safety Analysis), and using proper PPE (Personal Protection Equipment) at the workplace are emphasized. • You will oversee the handling and upkeep of the chemical and solvent store, preparation of Spec-check, catalog, and result entries, as well as maintaining volumetric solutions and reagents. • Your role also includes preparation of out lab testing samples (as required), timely destruction of samples as per SOP and any additional responsibilities assigned by the Group Leader. Qualification Educational qualification: A Bachelor’s degree in Chemistry, Analytical Chemistry, or a related field Minimum work experience : 2 to 5 years of experience in a laboratory setting, preferably in the pharmaceutical or related industry Skills & attributes: Technical Skills • Proficient in various analytical techniques, including sampling and analysis of raw material samples. • Experience with the operation and maintenance of analytical instruments like HPLC, GC, Potentiometer, Particle Size Analyzer, XRD, ensuring proper use and care as per SOPs. • Competent in LIMS activities related to sample tracking, documentation, and data entry. • Knowledgeable about cGMP, SOPs, and STPs, ensuring accurate documentation and adherence to specifications. • Adheres to safety precautions and procedures during analysis, emphasizing the importance of lab safety, JSA (Job Safety Analysis), and proper use of PPE (Personal Protective Equipment). • Expertise in handling and upkeep of the chemical and solvent store, including the preparation and maintenance of volumetric solutions and reagents. Behavioural Skills • Keen attention to detail in analysis and documentation, ensuring accuracy in all tasks. • Effective communication and collaboration skills for communicating with the Group Leader, reporting discrepancies, incidents, and providing timely updates. • Takes initiative in ensuring the proper use and care of instruments, timely destruction of samples, and other assigned responsibilities. • Demonstrates problem-solving skills in addressing discrepancies, incidents, and ensuring smooth laboratory operations. • Upholds ethical standards, compliance with SOPs, and follows regulatory requirements in all activities. 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/#!/

Job description Candidate will be based at corporate office of reputed Pharma company as a Manager- IT and he will be responsible for handling following:- Job Responsibilities: 1 Candidate would be responsible for the Servers and Computers, Printer and accessories are working properly any given time. 2) The Master Creation in the SAP Batch master is to be done properly. Backup of Servers and Computers are done from time to time. And functions of all camera system installed at plant to ensure proper support to the users.to prepare Presentation, SOPs and participate etc. for the IT compliance training. 3) He have good knowledge of administer LAN, WAN, EPABX & Video Conferencing. 4) Candidate would be responsible Daily Monitoring of all IT compliance with respect to Quality Assurance activities. IT compliance and data integrity Training to IT Team Members. Creation and Review of Qualification/ Validation related documents. Review of IT Training Matrix and Internal Trainer list. 5) Candidate would be responsible impart GSP, GLP, Behavioural, Motivational and other kind of trainings (Classroom & QC), ensuring compliance of the specified procedures / guidance and review of qualification documents such as URS, DQ, IQ, OQ, PQ and validation protocols and validation study report. 6) Candidate would be responsible for various Regulatory and Customer audits and assist management in providing compliance to audit observations and to review performance of juniors and recommend for higher punishment in case of their indulgence in any kind of misconduct including any data integrity. 7) Candidate would be responsible implementation and operation of Document Management (DMS), Quality Management System (QMS), Training/Learning management system (LMS), Lab Info. Management (LIMS) Software. 8) Candidate would be responsible troubleshooting any issues in SAP and subsequent validation and documentation of any modifications, enhancement or upgrades in any and all softwares implemented in the facility. 7) Candidate will be responsible for monitoring the performance of factory network, conduct regular internal audits and implement necessary modifications or adjustments to optimize resources.and CSV Activities with GAMP5 Approach with a yearly planner. And define and manage IT Disaster recovery strategy and Compliance and security for all IT related systems and infrastructure. Required candidate profile Qualification- Bachelors degree in Computer Science, Computer Application. . Candidate should have 8 to 12 yrs. in relevant experience in Hardware & Software. Candidate should have good experience in SAP, of Document Management (DMS), Quality Management System (QMS), Training/Learning management system (LMS). Candidate should have good Knowledge of LAN, WAN, EPABXETS. Should have good Knowledge of Daily Monitoring of All IT Compliance

Job Title: Informatics Qualification Postgraduate in Science/MCA with a minimum of 10- 18 years of IT experience in the Pharmaceutical / Life science domain Technical Skills Experience in demonstrating a track record of delivering scientific solutions in the pharmaceutical and CRO industry. Experience in the implementation of Informatic applications like (Electronic Laboratory Notebooks(elNB), Laboratory Information Management System, Chromatography Data system (CDS) and other scientific applications. Experience with Software development life cycle (SDLC) and Computer System Validation (CSV). Should have experience in running projects with CSV life cycle. Candidate should have knowledge of current regulatory & Guidelines (GAMP5) for CSV, i.e. 21 CFR Part 11 ERES, Part 820, Part 210 & 211, EU Annex 11, ICHQ9 and SOP requirements of computerized systems w.r.t. data security, traceability and integrity. Candidate should be familiar with GCP, GLP and GMP guidelines/SOPs. The candidate should have skills in managing Regulatory & Client Audits (experience in supporting internal and external audits). Other Skills: Strong leadership, communication, consulting and influencing skills. Must have experience in resource management - channelizing resources to track current and future program resource assignments. Must have excellent team collaboration skills and the ability to lead and motivate cross-functional teams. Strong analytical and communication skills are required. Roles and Responsibilities: Responsible for supporting informatics applications of the assigned departments. In collaboration with the scientific community identify, evaluate and implement software applications meeting business requirements. Implement new projects/solutions as per business needs. Coordinates between scientists and vendors for any solution development/implementation Ensure effective utilization of scientific systems and applications Coordinate with Syngene clients and/or vendors to roll out scientific applications extended to Syngene Facilitate computer system validation and ensures that scientific applications are GxP compliant as per the operating unit requirements Responsible for ensuring 21 CFR Part 11 compliance for enterprise & standalone applications Focus on near-zero downtime for enterprise applications Technical support and administration of scientific and associated applications. Challenges / error handling, escalation and troubleshooting of scientific and associated applications. Responsible for effective coordination among clients, operating unit and internal IT team for the application / infrastructure challenges faced by the operating unit to minimize or eradicate the downtime Responsible to provide the right solution for the challenges faced by the operating units Responsible for implementation / suggestion of any IT related process improvements for the operating units Location: Bangalore

Role Overview As a Quality Control Executive at Minar Spices , you will be the guardian of our spice products’ purity, safety, and consistency. You’ll design and execute testing protocols, inspect incoming raw materials and finished goods, and collaborate closely with procurement, production, and R&D teams to ensure that every batch meets—then exceeds—industry and regulatory standards. Key Responsibilities Incoming Material Inspection: Sample and test raw spices and additives for moisture, foreign matter, microbial levels, and aflatoxins. Approve or reject incoming lots based on predefined specifications. In-Process Monitoring: Conduct periodic checks on grinding, blending, and packing lines for particle size, aroma, color, and weight accuracy. Record observations, troubleshoot deviations, and recommend corrective actions. Finished Product Testing: Perform organoleptic evaluations (taste, smell, visual), physico‑chemical analyses (pH, moisture, volatile oil content), and microbiological assays. Issue Certificates of Analysis (CoA) for customer shipments. Standard Operating Procedures (SOPs) & Documentation: Develop, update, and enforce QC procedures, work instructions, and batch‑wise test records. Maintain traceability logs, calibration records, and raw material/finished goods registers. Regulatory Compliance & Audits: Ensure adherence to FSSAI, ISO 9001, HACCP, and other relevant certifications. Coordinate internal and external audits; implement corrective and preventive actions (CAPA). Supplier & Customer Coordination: Communicate quality requirements to suppliers; conduct periodic supplier assessments. Address customer quality queries, lead investigations on non‑conformances, and propose solutions. Continuous Improvement: Analyze quality data (rejections, customer complaints, lab results) to identify trends. Lead small projects (5S, Kaizen, Lean) to enhance process reliability and reduce waste. Qualifications & Experience Bachelor’s degree in Food Science, Food Technology, Chemistry, Microbiology, or a related field. 2–5 years of hands‑on QC/QA experience in spices, food processing, or FMCG industry. Strong understanding of spice chemistry, microbiology, and regulatory norms (FSSAI, ISO, HACCP). Technical Skills & Competencies Proficient with lab instruments (moisture analyzer, pH meter, basics of gas chromatography). Sound knowledge of organoleptic evaluation techniques for spices. Excellent documentation skills and familiarity with LIMS or ERP‑based QC modules. Analytical thinker with meticulous attention to detail. Strong communication skills—for cross‑functional teamwork and supplier/customer interactions. Ability to manage multiple priorities and work under tight timelines. Job Type: Full-time Pay: ₹30,000.00 - ₹38,000.00 per month Benefits: Cell phone reimbursement Provident Fund Schedule: Day shift Supplemental Pay: Commission pay Performance bonus Yearly bonus Work Location: In person

In this vital role you will join a multi-functional team of scientists and software professionals that enables technology and data capabilities to evaluate drug candidates and assess their abilities to affect the biology of drug targets. This team implements LIMS platforms that enable the capture, analysis, storage, and report of pre-clinical and clinical studies as well as those that manage biological sample banks. The ideal candidate possesses experience in the pharmaceutical or biotech industry, strong technical skills, and full stack software engineering experience (spanning SQL, back-end, front-end web technologies, automated testing). Roles & Responsibilities: Design, develop, and implement applications and modules, including custom reports, interfaces, and enhancements Analyze and understand the functional and technical requirements of applications, solutions and systems and translate them into software architecture and design specifications Develop and execute unit tests, integration tests, and other testing strategies to ensure the quality of the software Identify and resolve software bugs and performance issues Work closely with cross-functional teams, including product management, design, and QA, to deliver high-quality software on time Maintain detailed documentation of software designs, code, and development processes Customize modules to meet specific business requirements Work on integrating with other systems and platforms to ensure seamless data flow and functionality Provide ongoing support and maintenance for applications, ensuring that they operate smoothly and efficiently Possesses strong rapid prototyping skills and can quickly translate concepts into working code Contribute to both front-end and back-end development using cloud technology Develop innovative solution using generative AI technologies Create and maintain documentation on software architecture, design, deployment, disaster recovery, and operations Identify and resolve technical challenges effectively Stay updated with the latest trends and advancements Work closely with product team, business team including scientists, and other stakeholders What we expect of you We are all different, yet we all use our unique contributions to serve patients. The [vital attribute] professional we seek is a [type of person] with these qualifications. Basic Qualifications: Masters degree and 1 to 3 years of experience in Computer Science, IT, Computational Chemistry, Computational Biology/Bioinformatics or related field OR Bachelors degree and 3 to 5 years of experience in Computer Science, IT, Computational Chemistry, Computational Biology/Bioinformatics or related field OR Diploma and 7 to 9 years of experience in Computer Science, IT, Computational Chemistry, Computational Biology/Bioinformatics or related field Preferred Qualifications: Experience in implementing and supporting biopharma scientific software platforms Functional Skills: Must-Have Skills: Proficient in a General Purpose High Level Language (e.g. Python, Java, C#.NET) Proficient in a Javascript UI Framework (e.g. React, ExtJs) Proficient in SQL (e.g. Oracle, PostGres, Databricks) Experience with Event-based architecture (e.g. Mulesoft, AWS EventBridge, AWS Kinesis, Kafka) Good-to-Have Skills: Strong understanding of software development methodologies, mainly Agile and Scrum Hands-on experience with Full Stack software development Strong understanding of cloud platforms (e.g AWS) and containerization technologies (e.g., Docker, Kubernetes) Working experience with DevOps practices and CI/CD pipelines Experience with big data technologies (e.g., Spark, Databricks) Experience with API integration, serverless, microservices architecture (e.g. Mulesoft, AWS Kafka) Experience with monitoring and logging tools (e.g., Prometheus, Grafana, Splunk) Experience of infrastructure as code (IaC) tools (Terraform, CloudFormation) Experience with version control systems like Git Experience with automated testing tools and frameworks Experience with the implementation of LIMS/ELN platforms such as Benchling, Revvity, IDBS, STARLIMS, Watson, LabVantage, etc. Experience handling GxP data and system validation, and knowledge of regulatory requirements affecting laboratory data (e.g., FDA 21 CFR Part 11, GLP, GCP) Professional Certifications (please mention if the certification is preferred or mandatory for the role): AWS Certified Cloud Practitioner preferred Soft Skills: Excellent problem solving, analytical, and troubleshooting skills Strong communication and interpersonal skills Ability to work effectively with global, virtual teams High degree of initiative and self-motivation Ability to learn quickly & work independently Team-oriented, with a focus on achieving team goals Ability to manage multiple priorities successfully Strong presentation and public speaking skills

Job Description: Should have extensive experience (15+) in SampleManager LIMS software development, including design, implementation, and maintenance of the software. Should have strong data management skills, including data modeling, data mining, and data analysis to ensure efficient and accurate data management. To be an effective SampleManager LIMS architect, one must have experience in developing SampleManager LIMS solutions using version 21.X or later. Should be proficient in SampleManager LIMS configuration, scripting, and customization. The SampleManager LIMS architect should have experience in working closely with clients to understand their requirements and develop solutions that meet their needs, ensuring their satisfaction with the product. Should be able to communicate technical information to non-technical stakeholders in a clear, concise, and effective manner, ensuring that all parties understand the project requirements and goals. Should build lasting relationships with clients by understanding their business objectives, providing excellent customer service, and ensuring their satisfaction with the product. Should be able to work effectively with project managers to define project goals, timelines, and deliverables. They should also be able to provide regular updates on the project's status and progress. Should have knowledge of JIRA and Agile way of working The SampleManager LIMS architect should be able to work effectively with developers to design and implement software solutions that meet project requirements. They should also be able to provide technical guidance and mentorship to ensure high-quality code and adherence to best practices. Should be able to identify and resolve conflicts or issues that arise during the project lifecycle. They should also be able to work with stakeholders to develop contingency plans and risk mitigation strategies.

Operate and maintain flow cytometers (e.g., BD LSRFortessa, FACSCanto, Cytek Aurora, etc.). Perform instrument calibration, quality control, and routine maintenance. Prepare biological samples (staining, viability assays, compensation setup). Design and optimize multicolor panels for flow cytometry. Acquire and analyze cytometry data using software such as FlowJo, FCS Express, or Cytobank. Document experimental procedures and maintain accurate records in LIMS or lab notebooks. Troubleshoot instrument and protocol issues and coordinate with technical support as needed. Train staff and collaborators on proper cytometry protocols and instrument use. Ensure compliance with biosafety and laboratory safety protocols. Job Type: Full-time Pay: ₹18,000.00 - ₹22,000.00 per month Benefits: Paid sick time Provident Fund Schedule: Day shift Work Location: In person

Scientific Business Analyst (Sr Associate) – ELN What you will do This role involves working closely with Amgen Research partners and Technology peers to ensure that the technology/ data needs for drug discovery research are translated into technical requirements for solution implementation. The role maximises scientific domain and business process expertise to detail product requirements as epics and user stories, along with supporting artifacts like business process maps, use cases, and test plans for the software development teams. This enables the delivery team to estimate, plan, and commit to delivery with high confidence and identify test cases and scenarios to ensure the quality and performance of IT Systems. You will join a multi-functional team of scientists and software professionals that enables technology and data capabilities to evaluate drug candidates and assess their abilities to affect the biology of drug targets. This team implements scientific software platforms such as Laboratory Information Management Systems (LIMS) that enable the capture of lab workflows & experimental data and Electronic Lab Notebooks (ELN) that act as Amgen’s System of Record ensuring data integrity and business continuity. You will implement and manage scientific software platforms across the research informatics ecosystem, and provide technical support, training, and infrastructure management, and ensure it meets the needs of our Amgen Research community. Roles & Responsibilities: Function as a Scientific Business Systems Analyst within a Scaled Agile Framework (SAFe) product team Serve as a liaison between global Research Informatics functional areas and global research scientists, prioritizing their needs and expectations Manage a suite of custom internal platforms, commercial off-the-shelf (COTS) software, and systems integrations Lead the technology ecosystem for in vivo study data management and ensure that the platform meets their requirements for data analysis and data integrity Translate complex scientific and technological needs into clear, actionable requirements for development teams Develop and maintain a product roadmap that clearly outlines the planned features and enhancements, timelines, and breakthroughs Identify and manage risks associated with the systems, including technological risks, scientific validation, and user acceptance Develop documentations, communication plans and training plans for end users Ensure scientific data operations are scoped into building Research-wide Artificial Intelligence/Machine Learning capabilities Ensure operational excellence, cybersecurity and compliance. Collaborate with geographically dispersed teams, including those in the US and other international locations. Foster a culture of collaboration, innovation, and continuous improvement. What we expect of you We are all different, yet we all use our unique contributions to serve patients. Basic Qualifications: Master’s degree with 1 - 3 years of experience in Life Sciences, Computer Science, IT, Computational Chemistry/Cheminformatics, Computational Biology/Bioinformatics or related field, OR Bachelor’s degree with 3 - 5years of experience in Life Sciences, Computer Science, IT, Computational Chemistry/Cheminformatics, Computational Biology/Bioinformatics or related field, OR Diploma with 7 - 9 years of experience in Life Sciences, Computer Science, IT, Computational Chemistry/Cheminformatics, Computational Biology/Bioinformatics or related field, OR Demonstrated expertise in a scientific domain area and related technology needs Excellent problem-solving skills and a passion for tackling complex challenges in drug discovery with technology and data Experience with writing user requirements and acceptance criteria in agile project management systems such as JIRA Experience with Benchling, Revvity, IDBS, or similar LIMS/ELN platforms Preferred Qualifications: 3+ years of experience in designing and supporting biopharma scientific software platforms. Good-to-Have Skills: Experience with Agile software development methodologies (Scrum) Experience performing or enabling data capture and analysis from instruments in a research laboratory or vivarium Ability to communicate technical or complex subject matters in business terms Knowledge of business analysis standard processes, DevOps, Continuous Integration, and Continuous Delivery methodology Experience with cloud (e.g. AWS) and on-premise infrastructure Experience designing and supporting ELN/LIMS platforms in biopharma Professional Certifications: SAFe for Teams certification (preferred) Soft Skills: Able to work under minimal supervision Excellent analytical and gap/fit assessment skills Strong verbal and written communication skills Ability to work effectively with global, virtual teams High degree of initiative and self-motivation Ability to manage multiple priorities successfully Team-oriented, with a focus on achieving team goals Strong presentation and public speaking skills What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now and make a lasting impact with the Amgen team. careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.