2096 Hplc Jobs - Page 7

Job Description 1. Preparation and review of operational packing materials list, Packaging materials specifications, Packaging materials specifications base documents, BOM, BPR (PAS X and SAP), In House Labels for Exhibit Batches, Pack Split Up and Pallet Matrix. 2. To provided technical support to Production, QA, QC and RA. 3. Review of Artwork, Shade cards and print proof etc. Initiate Change controls, Deviation and CAPA and close all action item of change control, CAPA and deviation within time frame preparation of investigation report of deviation. Coordinate with R&D and QA for Primary Packaging Materials Specifications, Primary Pack Specification and Standard Test Procedures. 4. Preparation and Review of SOP’s, Protocols and Reports. Supervise compliance to all cGMP or any other regulatory requirements, including EH&S requirements. Execute and supervise all tasks and activities as per applicable SOP’s. Work Experience 2-4 years Education Graduation in Pharmacy Diploma in Packaging Technology Competencies Innovation & Creativity Result Orientation Collaboration Customer Centricity Developing Talent Stakeholder Management Strategic Agility Process Excellence

About The Role Data Executive

Roles and Responsibilities Conduct quality control tests on pharmaceutical products using instruments such as HPLC, UV, spectrophotometer, etc. Ensure compliance with cGMP guidelines and regulatory requirements. Maintain accurate records of test results, batch records, and inventory management. Collaborate with cross-functional teams to resolve issues related to product quality and stability. Perform routine maintenance tasks for laboratory equipment to ensure optimal performance.

Urgent Openings for QA,QC Executive Location : Tiptur, Halkurike Experience: Freshers Salary:14.5K in hand+ ESI, PF Qualification: MSc Chemistry only (Only Male candidates) Contact :6364467264 Food, OT Facility Tiptur to company to way cab

Role & responsibilities Provide Support to routine analysis of API Synthesis R&D and Stability samples. Documentation of Daily analysis in corresponding product LNB. Development of analytical methods for drug substances, raw materials and intermediates. Perform AMV, AMDR, AMT activities. Preparation of Analytical method validation / AMT protocol & report. Preparation of Tentative STP/MOA during Development. Trouble shooting at the time instrument operation and analytical method related problem. Preparation of COA, MOA and provide to LIMS. HPLC and GC Calibration and Documentation and provide GLP for the same. Prepare method development report. Analytical method transfers and Documentary Methods Transferring new analytical techniques to Quality control. Development and validation of cleaning method for drug substance

Job Track Description: Requires relevant expertise in a professional, sales, or technical area through formal education. Performs technical-based activities. Contributes to and manages projects. Uses deductive reasoning to solve problems and make recommendations. Interfaces with and influences key stakeholders. Leverages previous knowledge and expertise to achieve results with teams and can complete work self-guided. College or university degree required. General Profile Requires knowledge and experience in own field. Will acquire on-the-job knowledge and skills. Develops an understanding of the company, processes, and customers. Uses existing procedures to solve routine or standard problems. Receives moderate guidance and direction from others. Functional Knowledge Requires expanded conceptual understanding of theories, practices, and procedures. Business Expertise Uses an understanding of key business drivers to accomplish work. Impact Impacts team through quality of service and information provided. Follows standardized procedures and practices to achieve objectives and meet deadlines. Leadership No supervisory responsibilities. Provides informal guidance to new team members. Problem Solving Uses existing procedures and technical experience to solve problems. Interpersonal Skills Exchanges complex information and ideas effectively. Responsibility Statements Tracks and reports business-critical project and people metrics for client operations. Finalizes the intercompany reconciliation process. Liaises with AP and the business. Prepares monthly and quarterly balance justifications and documentation. Prepares customized reports and dashboards. Keeps updated data readily available for presentations or reporting. Performs other duties as assigned. Complies with all policies and standards.

Dear Applicants, Greetings from Biophore India !! We have opening for Formulation AR&D Department. Experience : 3 7 Years Qualification : B. Pharm /M. Pharm or M Sc Work Location: R&D Centre -Pashamylaram, Isnapur, Sanga Reddy. Job Description 1) Method Development and routine analysis of Assay, Dissolution, Related substances, Content Uniformity, Blend Uniformity. 2) Responsible for Analytical Method Validation activities for solid orals and injectables. 3) Responsible for Routine and Stability analysis activities for solid orals and injectables. 4)Responsible for the Review of documents generated in Method development activity. 5)Responsible for the Preparation and Review of Tentative method of analysis and Method development Reports. Please Carry below documents: 1. Updated resume. 2. Last 3 months pay slips or bank statement 3. Offer letter or Increment letter from the present employer,4. Photocopies of all Education certificates Ref to Friends or colleagues. Contact Person- Prasad- HR Interview Date: 13 -09-2025 (Saturday) Time:9:30AM 2:00 PM

Job Description Join Lupin Limited's dynamic Quality division as an Officer within our Validation department based in Pithampur. In this pivotal role, you will take charge of the cleaning validation activities for our API and Formulation facilities. Your responsibilities will encompass comprehensive management and execution of validation protocols supporting our commitment to the highest quality manufacturing standards. Your core duties will include ensuring rigorous residue cleaning validation processes to maintain contamination-free production environments. You will manage and evaluate nitrosamine and genotoxic cleaning validation activities, essential to safeguarding product safety and regulatory compliance. In addition, you will perform risk priority number (RPN) calculations to identify and mitigate potential risks effectively. Campaign studies including CEHT/DEHT will fall within your scope, enabling process optimization and validation integrity. The role extends to qualification activities for facilities, equipment, utilities, and HVAC systems, ensuring all operate at validated standards aligned with industry and regulatory requirements. As the Officer, you will prepare and review validation-related documentation with precision, supporting audit readiness and continuous improvement initiatives. Your efforts will directly contribute to Lupin's mission of delivering safe, efficacious pharmaceutical products to global markets. We seek an individual with a keen eye for detail, exceptional organizational skills, and the ability to collaborate cross-functionally. Your proactive approach to validation and quality processes will drive success and uphold our high standards. At Lupin Limited, you will be part of a culture that values innovation, strategic thinking, and continuous development. Join us to advance your career in a challenging and rewarding environment where your expertise makes a meaningful difference. Work Experience Applicants should have between 2 to 5 years of relevant experience in pharmaceutical cleaning validation or quality assurance sectors. Experience in executing and managing cleaning validation protocols, facility and equipment qualification, as well as working knowledge of regulatory requirements related to pharmaceutical manufacturing, will be highly valued. Education Graduation in Pharmacy Competencies Strategic Agility Innovation & Creativity Customer Centricity Developing Talent Result Orientation Process Excellence Collaboration Stakeholder Management

Key Responsibilities: Perform routine and non-routine chemical analyses of raw materials, in-process samples, and finished products using various laboratory instruments (e.g., HPLC, GC, UV-Vis, FTIR). Calibrate, maintain, and troubleshoot laboratory instruments to ensure accurate and reliable results. Prepare and review Standard Operating Procedures (SOPs) for analytical methods and ensure compliance with quality standards. Analyze data from testing and document results in reports, ensuring proper record-keeping and traceability. Conduct stability studies and product testing to ensure that products meet specifications. Work closely with production teams to resolve any quality-related issues and recommend corrective actions. Assist in the development and validation of new analytical methods. Ensure compliance with Good Laboratory Practices (GLP) and relevant regulatory requirements (e.g., GMP, ISO). Perform equipment maintenance and troubleshooting to ensure continuous operation of testing instruments. Assist in the preparation for internal and external audits and inspections. Qualifications: Bachelors degree in Chemistry, Biochemistry, or a related field. Proven experience (2+ years) in a Quality Control role within a laboratory or pharmaceutical/chemical industry. Familiarity with lab instruments such as HPLC, GC, UV-Vis spectrophotometer, and other analytical techniques. Strong understanding of GLP, GMP, and regulatory standards. Excellent attention to detail and ability to work independently. Strong analytical and problem-solving skills. Good communication and documentation skills. Ability to work under pressure and meet tight deadlines.

We will count on you to Drive the strategy and delivery of the US&CA catastrophe modelling analytics and advisory solutions from India based team. Develop & embed a consistent, curiosity driven and value proposition focused mindset across all our US&CA catastrophe modelling team members who work very closely with multiple onshore teams. Stakeholder Management - ability to govern project deliveries and manage end client expectations through reporting and performance metrics; lead change initiatives with stakeholders; demand gathering and resource planning through stakeholder agreement. Ensure a consistent engagement model between our operations and the onshore teams. Identify best practice within the existing teams, and points for improvements. Helping our US&CA region team in their capability and career development through training, performance management and continuous communication. Gets hands-on understanding of all aspects of the work being done by the team and be seen as a leader on all re/insurance analytics capabilities especially exposure management, and catastrophe modelling. Build an environment of innovation in the team; able to conceptualize new tools and products in line with the future needs of GC & GAA team and clients. Provide management support to Mumbai teams in the testing, feedback, and adoption of modernization work and products to drive efficiencies and insights through automation and standardization. Understands the end-to-end value chain of reinsurance across GC and is able to drive a change by bringing together talent from cross departments/teams. What you need to have: 2-10 years of experience in managing mid to large sized teams with significant experience in managing catastrophe modelling teams especially in re/insurance portfolio analytics and placements. Leading expertise on the operation of key vendor models (Moodys RMS, Verisk AIR, CoreLogic RQE etc.) and their application for re/insurance clients needs. Excellent communication skills to own interactions with onshore leaders. Proven track record of managing model adoption & change management process for re/insurers. People focused lead by example and create career paths for everyone. Talent management ability to attract, grow and retain key talent. Execution, Accountability, Reliability are key pillars of this role proven capability to build trust and be a positive force for leading change. What makes you stand out? Relevant market certifications e.g. ACII, CPCU, ARe etc. would be an added advantage.

As an Officer/Senior Officer in the Quality Control department located in Kandla, you will be responsible for handling troubleshooting of HPLC and GC analysis using Chromeleon Software. Your primary task will be to ensure that all work is carried out in compliance with SOP/STP/CSOP/GTP, including adhering to GLP and EHS norms, while maintaining laboratory discipline. It will be your duty to review and maintain all related log books and wet Laboratory records in a timely manner. Your role will also involve overseeing the completion of daily activities and targets, managing HPLC columns, and handling software such as LIMS, LMS, IMS, and SCM. You will be expected to identify gaps in SOPs, analytical worksheets, STP, GTP, etc., and take the necessary steps to update the relevant documents. Additionally, you will be responsible for maintaining all QC SOPs in the display copy, performing calibration activities for all QC instruments as per the schedule, and ensuring the upkeep of the GLP working area. Furthermore, you will be required to conduct and maintain the calibration of HPLC, monitor column management, and analyze in-process, finished product, and stability samples using the HPLC instrument. The ideal candidate for this role should possess a BSC/B Pharma qualification with 4-6 years of experience, preferably from the pharmaceutical industry. If you are detail-oriented, proactive, and have a strong background in quality control, we encourage you to apply for this position and contribute to our team's success.,

You will be responsible for carrying out quality control procedures at our new Agrochemical Plant. As a Quality Control Chemist, your main task will include operating various laboratory equipment and machinery such as HPLC, GLC, pH meter, Spectrophotometer, Hot air oven, IR, etc. The minimum required qualification for this position is a Master's degree in Chemistry (M.Sc. Chemistry). This is a full-time job opportunity suitable for freshers looking to kickstart their career in the field of Quality Control. Your work location will be in person at our Agrochemical Plant. Join us and be a part of our dynamic team dedicated to ensuring the quality of our products.,

Date: 1 Sept 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Development Services Job Title: Analyst Job Description At Syngene, Safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and sops, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to companys integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngenes quality standards always Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Job Description Analysis of Raw material/ In process / intermediate and finished product Handling of HPLC/GC/UV/KF /FTIR and other analytical instruments Sampling of Raw material / Intermediate/ Finished product Handling QMS activities Instrument calibration and qualification Maintained the Lab as per GMP requirements. Reserve sample management Experience : 1- 4 years Education M.Sc in general or organic chemistry Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status regarding public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities Show more Show less

Plant :- Pharmaceutical formulations Qualification :- Bsc /MSc Chemistry/Pharma Experience :- 1 - 2 year ( HPLC /GC KNOWLEGDE REQUIRED ) Job Time :- 9am to 6pm / 8.30 HRS Salary :- 15500 - 25000 ctc Travel : Gorva savli Road to Manjusar) Required Candidate profile Lab work to develop and improve both new and existing chemical product Mo No : +91 90816 99400 / +91 90816 88100 / 90816 99400

Job Track Description: Requires relevant expertise in a professional, sales, or technical area through formal education. Performs technical-based activities. Contributes to and manages projects. Uses deductive reasoning to solve problems and make recommendations. Interfaces with and influences key stakeholders. Leverages previous knowledge and expertise to achieve results with teams and can complete work self-guided. College or university degree required. General Profile Requires knowledge and experience in own field. Will acquire on-the-job knowledge and skills. Develops an understanding of the company, processes, and customers. Uses existing procedures to solve routine or standard problems. Receives moderate guidance and direction from others. Functional Knowledge Requires expanded conceptual understanding of theories, practices, and procedures. Business Expertise Uses an understanding of key business drivers to accomplish work. Impact Impacts team through quality of service and information provided. Follows standardized procedures and practices to achieve objectives and meet deadlines. Leadership No supervisory responsibilities. Provides informal guidance to new team members. Problem Solving Uses existing procedures and technical experience to solve problems. Interpersonal Skills Exchanges complex information and ideas effectively. Responsibility Statements Tracks and reports business-critical project and people metrics for client operations. Finalizes the intercompany reconciliation process. Liaises with AP and the business. Prepares monthly and quarterly balance justifications and documentation. Prepares customized reports and dashboards. Keeps updated data readily available for presentations or reporting. Performs other duties as assigned. Complies with all policies and standards.

Location:-Dahej (Bharuch) Industry:- Agro chemical Qualification:-Bsc /Msc chemistry/ Dip chemical *Experience:- Fresher * *Post :-Plant operator * Job time:- 8 hrs shift duty Salary:- 17400 ctc Facility:- travel + canteen Job type:- Permanent Required Candidate profile Perform In-Process Quality Control (IPQC) during tablet MFG. compliance with cGMP,coordinate with QA, QC, and Maintenance.

Following Good Laboratory Practices while working in the QC Laboratory. To maintain and clean responsibility allotted for individual instruments. Use of required safety apparel while sampling, analyzing, and working in the laboratory. Carry out the analysis of validation samples as per the protocol. Initiation of laboratory incidents and deviation. Preparation of calculation sheets and making draft reports. Disposal of sample for analysis after use. Taking any other job allocated by HOD or Section Head. Analysis of Intermediate, finished product, and working standard qualification as per the specification. Ensure that the instrument usage log is verified and reviewed periodically, and check the labels accordingly as per SOP. Preparation of protocols and Observation data sheets. Should be well versed with the latest analytical techniques like HPLC/GC, KF/KFC, IR/UV, LC-MS, GC-MS, IC, and ICP-OES/ICP-MS, etc... Being well-versed in the Chromeleon data management application and LIMS will be advantageous .

Job Overview TE Connectivity's Quality Control and Reliability Teams ensure product and / or product components comply with specifications and quality standards. They test and inspect products against performance and integrity criteria to ensure product quality and reliability, and to determine the suitability of product release. Responsibilities Understand Customer drawings, Technical requirements, Quality requirements, CSR and cascade the requirements to CFT Exposure to Design and process validation testing and understanding test specifications AQE engineers are part of the project core team and being the Voice of the customer as well as the interface to other internal departments Hands on experience in creating and reviewing PPAP documents such as PFC / PFMEA / DFMEA / Control Plan / Specifications reviews / preparation of control plan / Gauge planning / SPC / MSA Support the FMEA meetings to achieve the quality standard, structure and content by capturing past failures and lessons learnt Conduct Pre-PPAP audit, share observation to the team and follow-up to close all the open points Leading customer audits and experienced in obtaining PPAP approvals from customer Support Safe Launch for New projects to ensure 0 customer complaints before hand over the project to manufacturing site Education and Knowledge BE/ B.Tech (Mechanical / Production / Automotive Engineering) Knowledge about various phases of Product and Process development ISO/IAFT 16949 requirements for New Product / Process development Indepth knowledge in APQP/PPAP/PFC/PFMEA/DFMEA/Control Plan/SPC/MSA etc Awareness on VDA 6.3 requirements and audit Knowledge in wiring harness, parts having plastic injection molding / metal stamping processes will be an added advantage Critical Experience Minimum of 6-8 years of hands on experience in IATF 16949 (Formerly TS 16949) Quality systems in Automotive industry Experience in conducting internal audits & facing external audit as per IATF 16949 Quality systems Well versed and experienced in handling APQP, PPAP activities Leading interaction with Customer & suppliers for part and process from quality aspects Competencies

Role: Officer - Quality Control / Quality Assurance Job Location: Nashik At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. Viatris empowers people worldwide to live healthier at every stage of life. We do so via: Access Providing high quality trusted medicines regardless of geography or circumstance; Leadership Advancing sustainable operations and innovative solutions to improve patient health; and Partnership Leveraging our collective expertise to connect people to products and services. Every day, we rise to the challenge to make a difference and here's how this role, will make an impact: Role Purpose We have Openings in Both QC (Lab / Microbiology / CSV) and QA(IPQA / Documentation / QMS / AQA) . Seeking for candidates (Male/Female) with sound qualification background to ensure the testing of drug product in Quality control lab and to ensure every product is of the highest quality. They shall be concerned with sampling, specifications, testing, documentation, release procedures which ensure that the necessary and relevant tests are carried out under the norms of cGMP. Role & responsibilities Candidate must have relevant experience in Quality control OSD and QMS and able to operate & maintain laboratory equipment/instruments (HPLC, GC, Malvern Particle sizer, dissolution apparatus etc.) as per procedure. To maintain documents as per GLP requirements. To ensure the calibration status of laboratory equipment & instruments. To report and involve in incidence/Deviation/OOS/OOT investigations. Candidate must have sound exposure in the Quality Control Laboratory to supervise and maintain documents and retention of records as per GMP requirements. To ensure the review of QC documents like analytical reports SOPS, Qualification, Logbooks, Raw data sheet, analytical records, calibration and ensuring compliance to observations with proper root cause and justifications. Candidates participate in initiation, review, and closure of OOS/OOT and monitor the CAPA with implementation in Track wise. To ensure the compliance of the Corrective and Preventive Actions (CAPA) necessitated through various activities such as Regulatory Audits, Market Complaints, and Product Recall & Annual Product Review in the QC if applicable. To support Quality Assurance / Compliance /Regulatory Systems, Processes and ensure Monitoring, Execution, Initiation of the Quality Management Systems in Quality Control laboratory. Qualification & Experience Candidate must be B. Pharm/ M. Pharma/ M. Sc In Chemistry Experience- Candidate must have 1 to 4 years experience in a reputed pharma industry. Candidates must be willing to work in shifts Candidate who have faced regulatory Audits like FDA & MHRA Audit will be preferred.

Adobe Systems India Pvt. Ltd. is looking for Computer Scientist 1 (C++) to join our dynamic team and embark on a rewarding career journey Conduct research and development in computer science. Develop and implement computer algorithms and systems. Collaborate with computer science and engineering teams. Monitor and report on computer science performance. Ensure compliance with computer science standards and protocols. Provide support and guidance on computer science matters.

Job Description Summary Come Join Our Software Integration Team!! Our main activity consists in setting up GE Vernova software in different environments for internal and external customers, supporting project activities and providing expertise in tailoring the components based on requirements. We have a hybrid work environment as we work from home, the office and travel to customer sites as needed. The integration engineer is a key member in all projects, being engaged throughout the full lifecycle (Development, Factory Acceptance Tests, Site Acceptance Tests, Cutover, Support). Job Description GE Vernova allows us to bring a significant contribution to the Worldwide Electrical Energy context. Delivering on life-critical solutions we are deeply immersed into the worlds of Transmission, Distribution, Asset Management and Market Management making sure we shape how the energy landscape looks today and tomorrow. Our teams breathe software-life into R&D, Services and Support for GE Vernova Electrification Softwares products while liaising with stakeholders and customers all around the globe. GE Vernova is a global provider of software, hardware, services, and expertise in automation and embedded computing. We offer a unique foundation of agile and reliable technology providing customers a sustainable competitive advantage in the industries they serve, including energy, water, consumer packaged goods, oil & gas, government & defense, and telecommunications. The activity within this office consists of development and implementation of: Energy Management Systems (EMS) Distribution Management Systems (DMS) Different specialized teams for distinct technical fields contribute to the realization of these systems. (hardware, communications, databases, HMI, applications). One of the activities, carried out in the mentioned context, is engineering for specific monitoring and control of power systems applications (power flow, short-circuit calculation state estimator, contingency analysis, optimization in power systems, voltage control, load frequency control, power reserve management, load forecast, stability analysis, transient regimes, modeling of the equipment, of the automation and protection systems in power plants and of the power grids, energy market models). Main job responsibilities: Development of the mathematical models of the physical phenomena in the power systems Software development for real-time applications (code, testing) Carrying out the analysis to define the specifications for the real time monitoring and control systems Commissioning of the EMS, DMS systems Engineering and code development for the EMS, DMS systems that meets the high standards. Parameterization, optimization, testing of EMS, DMS systems Databases management Good technical background is required. The development of professional skills is achieved, in time, by involvement in the team activities and by trainings. Knowledge of the power systems phenomena and processes and related mathematical models(power flow, state estimator, short-circuit analysis, contingency analyst, voltage control, load-frequency control, power systems optimal regimes, load forecast, stability analysis, transient analysis, modeling of equipment and of automation and protection systems in power plants and power grids, DTS, models for the energy market) C C ++ programmer skills or similar Exposure in Modelling of SCADA and Power System Analyst Applications Familiarity or development experience on Windows OS or UNIX OS Qualifications Requirements Master's degree in Power Systems with 2 to 5 years of experience in the PSA Domain Troubleshooting skills Fluent in English Ability and willingness to travel Desired Characteristics Technically good performer who can integrate and test complex software systems to completion with a minimal supervision Excellent communication skills (verbal and written) Rigorous, methodical, well organized and self-disciplined Take initiatives, good trouble-shooter and autonomous Adaptability, reactivity and Availability Ability to analyze complex topics and make a verbal/written synthesis Ability and willingness to travel Network & Links Internal: Operations, Product Development, Tendering, and Maintenance & Support External: Customers, Partners Performance Measurement On Time Delivery Costs deviation + Committed budget (effort) deviation Software Delivery Processes Compliance Customer Satisfaction In collaboration with Methods & Tools Drive excellence in execution through continuous improvement and change management to implement competitiveness improvement initiatives (costs base reduction, lead time reduction, DevOps framework, productivity improvement, quality improvement) Monitor the efforts performance measurement indicators In collaboration with Maintenance & Support Ensure a smooth transfer to maintenance of ending projects through coordinated knowledge transfer. Can be solicited to provide some back-end support to maintenance team as part of the maintenance contract Customer Management Comply and contribute to elaboration of relevant Quality Procedures, work instructions and Processes in Quality Management System Report or resolve any process non-conformances in a timely manner Health and Safety Sets the example by demonstrating the proper acts and actively observes work conditions. Routinely observes routines and behaviors of others and provides immediate feedback regarding unsafe behavior and celebrates achievements or safe behaviors. Actively and routinely promotes the identification of hazards and near misses.

Job Title: Analyst Job description At Syngene, Safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and sops, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards always Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Job description 1. Analysis of Raw material/ In process / intermediate and finished product 2. Handling of HPLC/GC/UV/KF /FTIR and other analytical instruments 3. Sampling of Raw material / Intermediate/ Finished product 4. Handling QMS activities 5. Instrument calibration and qualification 6. Maintained the Lab as per GMP requirements. 7. Reserve sample management Experience : 1- 4 years Education M.Sc in general or organic chemistry Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status regarding public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities

JOB DESCRIPTION Designation: Senior Research Associate (9-II) Job Location: Bangalore Department: DAS About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation . Job Purpose: Senior Research Associate (9-II) is to work as team member in preparatory HPLC purification team. Key Responsibilities: High throughput purification of reaction mixture, utilizing mass-triggered reverse phase preparative HPLC. Able to utilize appropriate purification methods based on physical and chemical properties of target molecules. Expertise in analytical method development and problem solving. Able to perform LCMS and HPLC analysis. Minor trouble shooting of instrument and experimental issues. Able to communicate effectively within team and with Chemistry functions. Laboratory compliance to the QA and applicable regulatory guidelines. Corrective and preventive actions as and where applicable. EHSS adherence. Other activities as defined from time to time assigned by the head of the department. Educational Qualification: M.Sc. (Chemistry/Analytical Chemistry) Technical/functional Skills: Practical knowledge of resolving simple instrument-related challenges . Thorough understanding of various analytical techniques and methods developments (LC-MS, HPLC and prepHPLC). Hands on experience using instrumental/commercial software for data processing Basic knowledge of wet analysis. Basic knowledge of chemistry is desirable. Must be a team player and be quick to adapt to the needs of end users Experience: 2 to 5 years of experience for Senior Research Associate (9-II). Behavioral Skills: Able to follow instructions and perform the tasks under the supervision of the project leader and section head Fair interpersonal skills Excellent attention to detail and record keeping Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status about public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Job Title: Executive API R&D 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 SunshineAs 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. Role : To execute activities related to R&D impurity synthesis, along with a group comprising of Research Officers/ Research Assistants under guidance from the Project Leader/Group Leader Job Description: Impurity Synthesis to avoid external procurement Literature search with respect to assigned project and its documentation Experimentation (Process development, optimization and validation) Analysis, interpretation (HPLC, IR, NMR, Mass and CHN) and documentation of data General Laboratory Management etc. Travel Estimate NA Job Requirements Educational Qualification M. Sc Experience Tenure : 2- 3 years Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let s create a brighter future together!

JOB DESCRIPTION Designation: Senior Research Associate (9-II) Job Location: Bangalore Department: DDS-SATT About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation. Job Purpose (1-2 Lines): Purification Scientist to work as a team member in purification team. Key Responsibilities: (Maximum 5-8 Points) Proven ability to independently develop analytical methods for both reverse-phase (achiral) and polar organic (chiral) separations, with experience in scaling up methods to preparative scale. Hands-on experience with preparative HPLC systems, including MS-based Prep HPLC; familiarity with LC-MS and UPLC techniques is a strong advantage. Skilled in performing minor instrument troubleshooting, calibrations, and recovery analyses as required. Excellent written and verbal communication skills. Strong adherence to company health, safety, and compliance protocols. Flexibility to undertake additional responsibilities from the Line Manager in alignment with business needs. Educational Qualification: M.Sc. in Chemistry / analytical chemistry Technical/functional Skills: (Maximum 4-6 Points) Preparative HPLC, MS based Prep HPLC, LC-MS, UPLC and SFC is an advantage. Experience: 3 to 5 years of hands-on experience in reverse phase Prep.HPLC or relevant area. Behavioral Skills: Must have very good communication skills Equal Opportunity Employer: