Designation: Environment specialist Job Location: Bangalore Department: EHSS 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 RD productivity, speed up time to market and lower the cost of innovation. Job Purpose: To Lead Environment management at Syngene Bangalore SEZ site Key Responsibilities: Work closely with the regulatory authorities and maintain good relations with stakeholders and work closely with locations/ sites/ corporate and ensure that all the legal and statutory requirement under environment protection are complied. Handle EHSS regulatory documentation To ensure and renew all the EHSS regulatory approvals/Licenses across Syngene sites within the stipulated timeline To submit all the legal forms related to EHSS within the stipulated time to the respective authorities To interact with regulatory authorities with matters concerning the legal requirements and permits with management suggestion Decide suitable methods for site waste disposal (viz. liquid, solid and gaseous waste) as per the norms prescribed by the local and central authorities and the Syngene norms To ensure proper handling and scientific disposal of solid waste and effluents (Hazardous and Non Hazardous) and ensure compliance for the licensing regulations for environmental requirements at the site/locations Adopt new technologies and engineering methods available in the market without compromising on the parameters described by the authorities in order to reduce the hazardous waste. Provide technical input for efficient operation of ETP/MEE/Others and analysis of various effluent streams generated at the site for treatment and disposal Lead environment management programs initiated at the site/Locations from time to time based on the Syngene EHSS Policy Drive ISO 14001 (Environment management System) requirements Train the subordinates and create awareness of the environment at the site, especially for stakeholders like the production and Engineering departments Visit the plant on a regular basis to check that the routine operations are being carried out without any problems and also pay surprise visits to check on the conditions at the plants Ensure Audit observations (internal/external) are closed and complied in line with the policy. Establish, implement and enforce safe work practices throughout the company Create awareness about the culture at site/location to all the people, including the contractors To support in drafting governance or directives towards EHSS procedures and policies for all Syngene Sites To share and support with strategic recommendations related to the performance of EHSS function To contribute towards continual improvement objectives under taken by EHSS department To check the documents prepared in the department and to review EHSS SOPs periodically Generate monthly management report highlighting Environment standards for the site /Locations like water consumed, effluent generated, hazardous waste, emissions etc Educational Qualification: Graduate in Chemical/Environmental sciences Technical/functional Skills: Well versed with MS Office (Word, PowerPoint, Excel) and MS Projects Good command in English both oral and written and customer service skills Good time-management skills Great interpersonal and communication skills Possess the knowledge and exposure to environment, health, and safety (EHS) practices Experience: 5+ years of experience in the field of Environment management Fair understanding of the CRO/CDMO/pharmaceutical business Experience in establishing and sustainable environmental practices Behavioral Skills: Ability to independently handle cross-functional teams with multiple stakeholders to ensure compliance to prevailing environmental regulations Commitment to Safety, quality and integrity 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 with regard to 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 Bangalore, India Job category Clinical Development Job Title : Competency Development Professional Department: Global Patient Safety,GBS Job Level :6 Are you passionate about developing and implementing innovative learning methodologiesDo you want to play a key role in enhancing the onboarding and training experience for employees in Global Patient Safety, BangaloreDo you have the interpersonal Skills to navigate in a complex stakeholder landscape and are you able to set direction and deliver resultsIf so, we want you to join our team as a Competence Development Professional. Read more and apply today for a life-changing career. The position: As a Competency Development Professional at Novo Nordisk, you will support the implementation and operation of the competency framework and the continuous learning design model. Work both independently and in collaboration with a team of highly skilled, committed, and enthusiastic colleagues across the functional areas in Global Patient Safety , Bangalore(GPS BLR) and across Novo Nordisk Organize and align onboarding programs across GPS, Bangalore. Support the training of employees. Define and implement relevant learning methodologies and supporting technologies to enhance the learner experience and output. Drive initiatives for innovative, fit-for-purpose process optimization and training. Assume responsibility, communicate information, and take action as essential parts of your workday. Qualifications: Should possess a bachelor s/master s degree in pharmacy /Lifesciences A minimum 6 years of Pharmacovigilance experience is desired. It is preferable to have exposure to training and co ordination activities within the domain Relevant experience and solid understanding of processes and regulatory requirements within pharmacovigilance A strong insight into the value chain within a pharma company Proven track record in establishing effective learning and development governance and working closely with stakeholders to ensure it creates value The ability to work independently in a continuously developing environment. Strong communication and interpersonal skills. Ability to thrive working across skill areas and cultures in a global organization. Demonstrate critical thinking and creative problem-solving abilities in addressing challenges. Design and implement comprehensive training programs for new employees to ensure smooth onboarding process About the department : Global Patient Safety Bangalore has global responsibility for surveillance of Safety and Quality of Novo Nordisk clinical development and marketed products and is responsible for global handling and reporting of adverse event reports. Working at Novo Nordisk At Novo Nordisk, we don t wait for change. We drive it. We re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales we re all working to move the needle on patient care. Contact To submit your application, please upload your CV and motivational letter online (click on Apply and follow the instructions). Deadline: Apply before 28th February 25 Disclaimer It has been brought to our attention that there have recently been instances of fraudulent job offers, purporting to be from Novo Nordisk and/or its affiliate companies. The individuals or organizations sending these false employment offers may pose as a Novo Nordisk recruiter or representative and request personal information, purchasing of equipment or funds to further the recruitment process or offer paid trainings. Be advised that Novo Nordisk does not extend unsolicited employment offers. Furthermore, Novo Nordisk does not charge prospective employees with fees or make requests for funding as a part of the recruitment process. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. Related jobs

Job description Bangalore, India Job category Procurement Department - S2C Corporate Procurement Are you passionate about driving sourcing activities and ensuring high customer satisfactionDo you have a knack for bringing new ideas to the table to improve existing processesIf so, we invite you to join our dynamic team as a Sourcing Professional at Novo Nordisk. Read more and apply today for a life-changing career. About the department In Corporate Procurement at Novo Nordisk, we develop strategies and execute improvement projects to optimize global indirect spend. The Sourcing Team in Bangalore is newly created to support the growth in our sourcing pipeline and is responsible for supporting category managers on various sourcing activities and execution of end-to-end sourcing projects across indirect categories in marketing and professional services, HR, digital and commercial services, travel, IT and RD, Lab Services. Our ambition is to become a key enabler of sourcing activities execution worldwide. By joining our team, you will embark on a career journey offering opportunities to grow as a professional. The position As a Advanced Analyst / Senior Analyst at Novo Nordisk, you will: As a Advanced Analyst / Senior Analyst , you will be driving sourcing activities related to indirect categories. You will potentially have the opportunity to work across categories, depending on the needs, and ensure high customer satisfaction from our stakeholders. You will be working hand-in-hand with our category managers in HQ (Denmark) to execute on sourcing activities and ensure that a correct sourcing process is followed. We value diverse and new perspectives, so we expect you to bring new ideas to the table to continuously improve our existing ways of working. Your main responsibilities will be: Manage end-to-end sourcing activities (from requisition to award) e.g., RFI/RFP/RFQ with close coordination with procurement stakeholders and business. Conduct detailed bid analysis to assess the factors driving the price variations. Ensure compliance with the procurement guidelines and procedures. Contribute to the success of the category strategies through interaction with category managers in Denmark and other internal stakeholders. Negotiate optimal pricing and commercial terms with the suppliers with a focus on the quality of the services delivered. Collaborate with internal and external stakeholders to identify and develop new suppliers based on business needs, as and when required. Drive digital excellence by using our eProcurement tool (Coupa). Qualifications We are looking for candidates who possess the following qualifications: Bachelor s degree from a reputed university. MSc/MBA preferred. 8+ years experience in source-to-contract. Experience working with global stakeholders. Strong understanding of the sourcing process and ability to drive it independently. Proactivity and solution-oriented mindset when it comes to solving tasks. Ability to work independently and take ownership. Ability to synthesize and communicate effectively. Experience with eProcurement tools, preferably Coupa. Experience working with indirect procurement categories, marketing, professional services, and consulting. Experience with eAuction, contract drafting, and market research. Pharma domain will be added advantage. Working at Novo Nordisk Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 63,000 employees around the world. We recognise the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk, we re working toward something bigger than ourselves, and it s a collective effort. Join us! Together, we go further. Together, we re life changing. Contact To submit your application, please upload your CV online (click on Apply and follow the instructions). Apply Now! Deadline 15th March 2025. Disclaimer It has been brought to our attention that there have recently been instances of fraudulent job offers, purporting to be from Novo Nordisk and/or its affiliate companies. The individuals or organizations sending these false employment offers may pose as a Novo Nordisk recruiter or representative and request personal information, purchasing of equipment or funds to further the recruitment process or offer paid trainings. Be advised that Novo Nordisk does not extend unsolicited employment offers. Furthermore, Novo Nordisk does not charge prospective employees with fees or make requests for funding as a part of the recruitment process. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. Related jobs

The Manager is extensively expected to be able to make decisions and set direction on behalf on Global Medical Affairs when it comes to matters within the job description The Manager acts as Subject Matter Expert for all products covered in his/her department and leads the timely, accurate and credible building of scientific and medical knowledge within the project including internal training. The Manager must drive and maintain communication to and from the external scientific community (including to provide medical and scientific support for key opinion leaders and HCPS) and within the organization. Communication and Stakeholder interaction: Key Internal Stakeholders: Medical Affairs (Medical Directors other Regional heads, MedAff HQ, National Medical Advisors, Field Medical Force) Marketing, Sales. Global Development Public Affairs, Regulatory and Quality. Global Medical Affairs management Brand and area Global Project Team (GPT)/ Lifecycle Management Team Core Brand Team (CBT) Local and international Health Care Professionals and Influencers (local and global Opinion Leaders) Medical, scientific and patient organizations Medical communication agencies Qualifications M.D. with substantial clinical and/or research expertise in relevant area (e.g. Endocrinology, Cardiology, General Practice or Internal Medicine) Strong clinical and/or research background in area of diabetes mellitus with interest in advanced scientific analysis and communication and experience in drug development. Understanding of the pharmaceutical industry. Fluency in both spoken and written English. Demonstrated research experience (e.g. publications) Additional education and experience in pharma business/marketing (preferable) Minimum one year of study or work in a country other than the native country (preferable) Additional education/scientific degree in research (e.g. PhD) (preferable) At least 10 years of clinical and/or pharmaceutical industry experience. At least 7-8 years of experience in a leadership role. Experience with clinical medicine, clinical research and development. Willingness to coach colleagues and support team development. Ability and willingness to quickly adjust to new situations in a continuously developing environment Ability to engage and collaborate with people with different backgrounds (science, business, etc) Excellent presentation skills. Strategic mindset. About the department Global Medical Affairs, GBS (GMA GBS) is an extension of the Global Medical Affairs team in Headquarters (HQ) in Denmark and Zurich and is based out of Global Business Services (GBS), Bangalore, India. The team consists of highly motivated scientific and medical advisors, project managers, medical illustrators and publication manager working together with HQ, regions and affiliates across the world. Our core competencies are communicating scientific and medical knowledge on our products to the external scientific community and across the organization; delivering external medical events including in-house content development and project management; and Publication planning. Working at Novo Nordisk Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 63,000 employees around the world. We recognise the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk, we re working toward something bigger than ourselves, and it s a collective effort. Join us! Together, we go further. Together, we re life changing. Contact To submit your application, please upload your CV and motivational letter online (click on Apply and follow the instructions) Deadline 25th February 2025 Disclaimer It has been brought to our attention that there have recently been instances of fraudulent job offers, purporting to be from Novo Nordisk and/or its affiliate companies. The individuals or organizations sending these false employment offers may pose as a Novo Nordisk recruiter or representative and request personal information, purchasing of equipment or funds to further the recruitment process or offer paid trainings. Be advised that Novo Nordisk does not extend unsolicited employment offers. Furthermore, Novo Nordisk does not charge prospective employees with fees or make requests for funding as a part of the recruitment process. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. Related jobs

Job Title: Lead Consultant - Product Data Engineer Career Level: E Introduction to role Are you ready to lead the charge in transforming data into actionable insights? As a Lead Consultant - Product Data Engineer, you will be at the forefront of designing, developing, testing, deploying, and operating data, advanced analytics, and AI products that support the US Oncology Business Unit. This role demands technical leadership, collaboration with platform engineering teams, and alignment with business strategies to translate needs into technical solutions. You will serve as a technical liaison for IT Capability and Business Engagement teams, ensuring the delivery of impactful data, analytics, and AI products. Stay ahead of the curve by keeping up with the latest advancements in data engineering, analytics, and AI technology to guide your team effectively. Accountabilities Lead design, development, testing, deployment, and operations for data, analytics, and AI products supporting the US Oncology Business Unit. Maintain deep working knowledge of US commercial datasets (Sales, Patient, Digital, etc.), their data lineage, business rules, important metrics, usage, and operations. Develop and maintain an in-depth understanding of data engineering and AI capabilities, staying ahead of with the latest advancements and industry trends. Collaborate with Global Capability, Business Engagement, Delivery, and Platform teams to drive the best customer experience and outcomes. Ensure products and solutions adhere to best practices and AZ architecture standards and strategy. Implement processes, tools, and automations to ensure developer productivity and quality. Provide technical expertise to peers and 3rd party development suppliers to ensure consistency with AZ IT and Commercial IT standards and processes. Work with platform delivery resources to validate business and functional requirements as part of product development responsibilities. Evaluate new technologies/application features and make recommendations for technology and business strategic roadmaps. Demonstrate expert understanding of AstraZeneca s application development processes for data products. Mentor junior staff members through technical training sessions and project output reviews. Establish partnerships with 3rd party suppliers for staff augmentation and project capacity, providing technical guidance for projects implemented through these suppliers. Serve as an internal consultant for IT and business partners across regions and business areas (Commercial, Medical). Continuous Improvement and Innovation Partner with Platform Success Leads on continuous improvement opportunities within platform and product-level backlogs. Identify new hardware/software technologies to fit specialized business needs and configurations. Identify issues with current processes and provide feedback on proposed changes to enhance IT effectiveness. Essential Skills/Experience Bachelor s degree or equivalent in Computer Engineering, Computer Science, or a related field 10+ years of experience in data/software engineering roles 5+ years of experience with building AWS cloud-based data pipelines 5+ years of experience with Python and Spark 3+ years of experience with Databricks, including Spark-based processing, data pipelines, and the platforms tools for analytics and machine learning Commitment to staying up-to-date with advancements in data engineering, AI, and Databricks features Experience in Continuous Integration and Deployment methods delivered as part of an agile team Ability to interpret and communicate technical information in business-friendly language Strong communication and interpersonal skills Proven experience managing and coaching/mentoring junior engineers Proven experience developing and managing relationships with 3rd party suppliers Strong written and verbal communication skills Experience working in a global organization with a complex geographical structure Desirable Skills/Experience Databricks certification Knowledge of machine learning concepts, including model training, evaluation, deployment, and monitoring within Databricks MLflow or other MLOps platforms Prior experience working in Pharmaceutical or Healthcare industry IT environment Experience with IQVIA Claims, National and subnational sales data Experience working within a DevOps delivery model Experience working within a quality and compliance environment and application of policies, procedures, and guidelines At AstraZeneca, our work directly impacts patients by transforming our ability to develop life-changing medicines. We combine pioneering science with leading digital technology platforms and data to empower our business to perform at its peak. Join us at a crucial stage of our journey to become a digital and data-led enterprise. Here you can innovate, take ownership, explore new solutions, experiment with powerful technology, and tackle challenges that have never been addressed before. With countless opportunities to learn and grow in a dynamic environment backed by significant investment, theres no better place to make a meaningful impact. Date Posted 17-Mar-2025 Closing Date 24-Mar-2025

Greetings from Synergy Resource Solutions, a leading recruitment consultancy firm. Our client is a 53 years old leading Hearing devices manufacturer & distributor for world-class hearing aids for India location. They are seeking a Field Sales Person for the Ahmedabad/Gujarat Location. Experience: 3 - 5 years Work days: Monday to Saturday Location: Candidate from Ahmedabad preferred Head Office: Chennai Job description: We are looking for a Business Development Manager to manage sales and Collections for the entire Gujarat region (medical/pharma sector preferred). Territory: Entire Gujarat Responsibilities: Conduct campaigning activity for the company brand promotions Plan and execute activities for the patient leads. Promotion, Distribution, advertising and branding activities planning Update the business development report to the management Create Sales Strategies and implementation Review and improvise and work accordingly. Plan and execute the business development and marketing plan periodically in concern with the superior and management, and close the monthly target. Close the Monthly Sale as per the target assigned Review the Market and prepare customer segmentation Follow up with existing and new potential retail Leads and convert to a new Centre Grow revenue from existing and new customer base Implement locally all national promotions and programs Maximize share in existing accounts Maintain consistent customer contact and relationship Market feedback on competitor s activity and offerings Required skills: Bachelor s Degree, Minimum 3 - 5 years of relevant experience in selling products to the Medical device industry, Pharmaceuticals, FMCG, Hospitals, Institutes, e-tendering businesses and Hearing aid centers Experience in generating new sales via cold calls Strong positive can-do attitude Willing to travel 100% Languages: English & Hindi (Gujarati Nice to have) Role: Business Development Manager - Sales Industry Type: Medical Devices & Equipment Department: Sales & Business Development Role Category: BD / Pre-Sales Education: Any Graduate If interested, Please share your updated resume with details of your present salary, expectations & notice period.

Job Title: SAP FICO - Senior Consultant Grade - D2 Introduction to role: Join a world-leading pharmaceutical company as an SAP Senior Functional Consultant. Operating in over 100 countries and headquartered in the United Kingdom, you will be part of a functional team for a large SAP support and maintenance project spanning several SAP landscapes across continents. Your expertise in the FI and CO modules, along with your broad functional knowledge, will be essential in driving success. Accountabilities: Resolve SAP issues reported by business users and deliver all changes and enhancements as required. Complete all tasks assigned by the team lead and project manager. Interact with business users for requirement gathering and provide timely updates on progress. Essential Skills/Experience: In-depth functional understanding of their respective work stream. Good understanding of business processes in the life sciences/pharmaceutical domain. Ability to understand business requirements from business users, prepare functional specifications, perform configuration changes, assist technical teams (e.g., ABAP) in their work, perform system and integration testing. Exposure to highly customized SAP environments and working on interfaces with Non-SAP systems. Very good understanding of integration of SAP modules in end-to-end business processes. Understanding of ITIL processes and Application lifecycle management. Ability to work in large and diverse teams. Desirable Skills/Experience: Exposure to Run SAP (Solution Manager) methodologies. Experience with various estimation techniques. Excellent communication and interpersonal skills. Proficiency in English, both spoken and written. Willingness to work in shifts. Proactive approach to problem-solving. Experience working in a globally distributed team. At AstraZeneca, we are at the forefront of digital transformation, leveraging our technologies, tools, and platforms to drive our journey forward. By uniting our expertise, we can better interpret data and make informed decisions that positively impact patients worldwide. Our collaborative environment empowers our diverse team to explore innovative solutions and continuously expand their knowledge. Ready to make a difference? Apply now to join our dynamic team! We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. 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. Date Posted 12-Mar-2025 Closing Date 25-Mar-2025

Job Title: Senior Consultant - Data Analyst Grade - D1 Introduction to role We are looking for a passionate Data Analyst for AstraZeneca, a world-leading pharmaceutical company operating in over 100 countries and headquartered in the United Kingdom. In this role, you will turn data into information, information into insight, and insight into business decisions. Accountabilities Work with business and IT partners to understand the business and data requirements. Acquire data from primary or secondary data sources and perform data profiling. Interpret data, analyze results, and provide quick data analysis. Identify, analyze, and interpret trends or patterns in complex datasets. Analyze multi-source data and create integration rules for the conformed layer. Understand data models and build mapping documents. Build bus matrices, proof of concepts, source mapping documents, and raw source data models. Identify and report data quality issues. Support data modelers and information architects with required information and analysis. Essential Skills/Experience Strong knowledge of and experience with Excel, databases (Snowflake, Postgres, Redshift, Oracle etc.) Solid experience on SQL and ability to write SQL queries to perform data profiling, data analysis and present the insights to the business. Good knowledge on Data warehousing and Data Modelling concepts. Exposure on overall Data management concepts. Strong Exposure to IT Project Lifecycle. Programming (Python, R) and ETL experience are value-adds. Life Science/Finance/SAP/SCM Domain knowledge and experience is an added advantage. Desirable Skills/Experience Any Bachelors or Master s Degree from a reputed institution. Preferable industry experience in IT or Pharma. 8-10 years of relevant experience. At AstraZeneca, we lead transformation by fusing our digital and data capabilities with strong business support. We take pride in positively impacting patients worldwide by leveraging leading technologies and exploring data to make improved decisions. Our ever-changing environment encourages innovation and bold new approaches. We empower our diverse team of specialists to explore and express their ideas, fostering continuous knowledge expansion and development. Our collaborative culture ensures that we work seamlessly with various partners, markets, functions, and people to drive success. Join us now to make a significant impact and enable many people to achieve more! We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. 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. Date Posted 14-Mar-2025 Closing Date 20-Mar-2025

Overview The health economics modeling practice specializes in helping clients determine, demonstrate, communicate and realize the value of pharmaceutical interventions, medical technologies and diagnostic testing by developing cost effectiveness, budget impact models and other decision-support tools. Our clients include pharmaceutical, biotechnology and medical device manufacturers for whom we provide strategic consulting, rigorous analytics, market-savvy communications capabilities, and evidence-based solutions. We are one of a few firms that integrate health economics, evidence synthesis, outcomes research, pricing and market access, with more than 180 consultants/researchers around the world. Position Description The HEOR practice is looking for a talented Consultant to help develop, design, and deliver health economic modeling projects. Consultants work with Analysts, Engagement Managers and Principals on each project. Occasional travel may be required. Responsibilities include: Design modeling studies to quantify clinical and/or economic impacts of healthcare technologies or interventions Contribute to development of project deliverables, including models, reports, abstracts, manuscripts, and slide decks, as appropriate Provide coaching and direction to more junior HEOR professionals assigned to engagement(s), especially regarding decision modeling and excel modeling technical expertise Help develop compelling proposals for new projects Consultants work across clients, therapy areas and projects, ensuring a cohesive professional environment and a deep and thorough understanding at all levels of the broad discipline of HEOR. In addition, Consultants will experience the following: Flexible and diverse work environment with a multidisciplinary team of researchers/consultants with backgrounds in medicine, pharmacy, health economics, health policy, health services research, outcomes research, pricing and market access Opportunity to engage in Center of Excellence to promote global best practices, collaboration and thought leadership in core offerings Formal and informal training opportunities in leading client engagements, statistical analyses, economic modeling, and scientific communications Qualifications The ideal candidate MUST have: Knowledge of health economic modeling techniques, including decision analysis Good interpersonal and communication skills in team environment Academic or work experience in a related area such as economics, health economics, statistics, engineering, or science Strong organizational skills and proven ability to manage personal responsibilities on multiple priorities and/or projects at once The successful candidate should also have: Graduate degree in relevant scientific or technical field (e.g., Medical Doctor, Pharmacy, Statistics, Economics, Mathematics, Engineering, Health Policy) At least 2-3 years of experience in applied research or consulting environment Proven ability to write and publish for medical or scientific audiences Expert-level proficiency in Microsoft Excel (including Visual Basic) Command of Microsoft Office, TreeAge, statistical software (e.g. SAS or STATA)

Primary Job Function Achieving assigned territory/ geography wise sales target Carrying out effective field work without direct day-to-day supervision Report field work in daily basis on assigned online system Meeting Call Average, Coverage, Frequency coverage Norms of assigned division Core Job Responsibilities Generate maximum prescriptions increase market share Promote the Division s products as per strategy Relationship Building with the Stake holders (Doctors, Chemists, Stockiest etc) Facilitating Strategy building A good Brand Ambassador Minimum Education BSc/B. Pharma. Experience/Training Required 2+ Yrs of experience Fresher with good communication and analytical skill may also consider Candidate with prior/current experience in same therapy Candidate from MNC and top Indian Pharma companies will have added advantage Fluent and confident in communication

Primary Job Function Achieving assigned territory/ geography wise sales target Carrying out effective field work without direct day-to-day supervision Report field work in daily basis on assigned online system Meeting Call Average, Coverage, Frequency coverage Norms of assigned division Core Job Responsibilities Generate maximum prescriptions increase market share Promote the Division s products as per strategy Relationship Building with the Stake holders (Doctors, Chemists, Stockiest etc) Facilitating Strategy building A good Brand Ambassador Minimum Education BSc/B. Pharma. Experience/Training Required 2+ Yrs of experience Fresher with good communication and analytical skill may also consider Candidate with prior/current experience in same therapy Candidate from MNC and top Indian Pharma companies will have added advantage Fluent and confident in communication

TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industrys broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in RD generates a steady flow of APIs, enabling timely introduction of new products to market. How you ll spend your day Excellent communication and with hands on experience. Having working experience of analytical method development/ validation for HPLC/GC test methods, from different markets. Troubleshooting/OOS investigations during validations. Having a good knowledge of HPLC, IR, UV, KF Titrator, Halogen Moisture analyzer, Polarimeter and wet analysis Having good knowledge of HPLC trouble shooting. Sound knowledge of Organic Chemistry Spectroscopy. Having a good knowledge of HPLC Method development of API/RM/KSM and SM using various detector like Mass, IR, CAD, ELSD, UV-PDA and UV. Structure elucidation and Identification and characterization of APIs, known and unknown impurities and intermediates by various spectroscopy techniques. Data interpretation by NMR, Mass Spectrometer, DSC, TGA FTIR Having a sound knowledge of Analytical method validation. Hands on experience of various Analytical Instruments-Coulometer, FT-IR, UV, Karl Fisher, Halogen Moisture Analyzer etc., >sound knowledge of Organic Chemistry Spectroscopy. Your experience and qualifications MSc (Organic chemistry/Analytical chemistry) 4- 7 year

Performing Stability analysis . Performing Method transfer/ Method Validation Analysis. Calibration and validation of instruments / equipment s Analysis. Preparation of Method Transfer Protocols (MTP), Method Transfer Report (MTR), Method of analysis (MTH), Test Data Sheet (TDS) for Stability Analysis and Method transfer / Validation any document related to stability analysis, method transfer / method validation in compliance with current guidelines Preparation of departmental SOP s in compliance with current guidelines. Preparation of validation protocols in compliance with current guidelines. Entry of stability sample results in LIMS / SAP. Handling of LSCMS Software. Your experience and qualifications M.Sc. (Chemistry) with 5 to 10 years of relevant experience

Performing Stability analysis . Performing Method transfer/ Method Validation Analysis. Calibration and validation of instruments / equipment s Analysis. Preparation of Method Transfer Protocols (MTP), Method Transfer Report (MTR), Method of analysis (MTH), Test Data Sheet (TDS) for Stability Analysis and Method transfer / Validation any document related to stability analysis, method transfer / method validation in compliance with current guidelines Preparation of departmental SOP s in compliance with current guidelines. Preparation of validation protocols in compliance with current guidelines. Entry of stability sample results in LIMS / SAP. Handling of LSCMS Software. Your experience and qualifications M.Sc. (Chemistry) with 5 to 10 years of relevant experience

Performing Stability analysis and review of documents Performing Method transfer/ Method Validation Calibration and validation of instruments / equipment s Preparation of Method Transfer Protocols (MTP), Method Transfer Report (MTR), Method of analysis (MTH), Test Data Sheet (TDS) for Stability Analysis and Method transfer / Validation any document related to stability analysis, method transfer / method validation in compliance with current guidelines Preparation of departmental SOP s in compliance with current guidelines Preparation of validation protocols in compliance with current guidelines Entry of stability sample results in LIMS Handling of LSCMS Software Your experience and qualifications M.Sc(Chemistry) with 5 to 10 years of experienc

Use Your Power for Purpose As a Senior Associate, you will play a crucial role in improving patients lives while working at Pfizer. Your contributions will directly impact the development and delivery of innovative solutions that enhance the quality of life for patients worldwide. Join us in our mission to bring breakthroughs that change patients lives. What You Will Achieve In this role, you will: Manage your own time to meet targets and develop plans for short-term work activities on moderately complex projects. Make decisions to resolve moderately complex problems in standard situations, working within guidelines and policies. Use your judgment to modify methods and techniques as needed. Collaborate with cross-functional teams to ensure project milestones are met. Provide technical support and expertise in the development and implementation of new processes and technologies. Here Is What You Need (Minimum Requirements) High school diploma (or equivalent) with 8+ years of experience or associate s degree with 6+ years of experience or BA/BS with 2+ years of experience or MBA/MS with any years of relevant experience . Strong technical skills in process development and optimization Proficiency in data analysis and interpretation Experience with project management tools and methodologies Knowledge of regulatory requirements and compliance standards Ability to work collaboratively in a team environment Strong communication skills, both written and verbal Proficiency in Microsoft Office Suite Bonus Points If You Have (Preferred Requirements) Experience in the pharmaceutical or biotechnology industry Familiarity with Good Manufacturing Practices (GMP) Experience with statistical software (e. g. , Minitab, JMP) Ability to lead cross-functional teams Strong organizational skills Adaptability and flexibility in a dynamic work environment Ability to mentor and develop junior team members Preferred Education/ Qualification: B. Pharm / M. Pharm /M. S (Pharmacy)/ M. Sc / BE Experience: 5+ years of experience in Quality assurance and /or Validation function of sterile dosage form facility. Core Competencies : Understanding of pharmaceutical manufacturing, packaging, quality assurance, and quality control operations. Knowledge of validation principles and practices related to the following areas: manufacturing process, analytical method, cleaning methods, facility, equipment, instrument, utility system, and CSV systems. Conversant with design & working principles of key equipment used in sterile manufacturing -Autoclave, Vial washing, Heat tunnel, Homogenizers, Vail filling, Filter integrity testing devices, Visual inspection equipment, Packing equipment, and Cleaning Validations. Well versed with Terminal process - design, execution and review. Experience in plant and TS operations. Good document review skills, data analysis with ability to identify issues and recommend actions Knowledge on the Qualification instruments and Tools. Knowledge on the GAMP requirements, PDA guidance, ISO guideline, 21 CFR part 11. Knowledge on the Components level assessment, PM requirement. Good knowledge on the Validation instruments calibration. Knowledge on the assessment of the Change controls and failure investigations. Knowledge of current validation regulations in the industry and validation principles. cGMPs and FDA regulatory guidelines. Strong Technical skills, leadership, organizational planning and project management skills, in addition to strong technical background required to coordinate multi-disciplinary teams. Strong interpersonal skills. Excellent interpersonal effectiveness and communication skills (written and oral) to interface across departments and management levels. Engineering #LI-PFE

Title: PV Scientist - Senior ExpertLocation: Bangalore Purpose of the Role: We are seeking a highly motivated and skilled Pharmacovigilance Scientist to collaborate with global safety leads and program safety leads This role is essential for providing integrated medical safety strategies for assigned investigational and core (high-risk) marketed products, including input into safety aspects of clinical development, risk management, and benefit-risk management Your roleSignal Detection and Management:Perform safety monitoring using dedicated tools (eg, Spotfire, EVDAS, Empirica Signals) for signal detection Review and analyze clinical and safety database outputs; interpret aggregate safety data from clinical trials and post-marketing sources Review scientific literature for safety surveillance and signal detection Support the analyses of safety signals, contribute to authoring signal evaluation reports, and participate in relevant safety governance meetings Support communication of findings from Emerging Safety Issue Reports to external stakeholders RMP Updates and Periodic Safety Reports:Retrieve/summarize data from various sources in support of authoring and providing content for Risk Management Plans (RMPs) and periodic safety reports Support local adaptation of RMPs and respond to health authority questions Submissions and Safety Variations:Contribute to delivery of safety relevant documents of the Common Technical Document (CTD) Contribute to ISS/SCS IAP, health authority briefing documents, and product information and clinical overview addendum Clinical Trial Activities: Provide input into safety sections of the Investigational Medicinal Product Dossier (IMPD), Investigators Brochure (IB), and Informed Consent Form (ICF) Support delivery of safety-related input for clinical trial documents, including protocols and reports Provide safety related input for data monitoring committees with safety-related documentation Other Activities:Respond to queries from auditors/inspectors and participate in interviews Contribute to the design and implementation of post-authorization safety studies Develop and maintain MedDRA CMQs for signal analysis and aggregate safety data Create product-specific training for internal and external stakeholders Provide expert input into process standardization and improvement within GPS and GD Who you are: Experience Required:MD, or PhD/advanced science degree or tertiary level qualifications in a biomedical/health related field Fluent in written and spoken English Qualification:Over 4 years of Pharmaceutical industry experience or similar (egHealth Authority) Experience in Pharmacovigilance risk management in both clinical development and post-marketing areas, including submission experience Ability to work collaboratively in a global team environmentTech savy with strong analytical and communication skills

As a Biostatistician II, you ll perform ad-hoc or exploratory analyses to support submission or Health Authority Questions. Having exposure to regulatory work experience is a bonus, for example, if you understand the regulatory questions and translating them to statistical problems, collaborating effectively, with clinical and regulatory colleagues. Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have: Master s degree in statistics or a related discipline. Ph.D. strongly desired. 3+ years supporting clinical trials in the Pharmaceutical or Biotechnology industry. Experience working for a CRO is strongly desired. Experience in sample size calculation, protocol concept development, protocol development, SAP, and preparing clinical study reports including integrated summaries for submissions. Good SAS programming skills for QCing critical outputs, Efficacy/Safety tables, and working closely with Programmers. Knowledge of R programming is a plus. Solid understanding & implementation of CDISC requirements for regulatory submissions. Adept in ADaM specifications generation and QC of datasets. The ability to build strong external & internal relationships and motivate a regional or global team. Effective communicator: able to explain methodology and consequences of decisions in lay terms. As a Biostatistician II, your responsibilities will include: Providing statistical support to clinical studies Participating in the development of study protocols, including participation in study design discussions and sample size calculations Reviewing CRFs and data review guidelines; developing statistical analysis plans (SAPs), including analysis dataset and TLG specifications Performing statistical analyses and interpreting statistical results Preparing clinical study reports, including integrated summaries for submissions Utilizing your strong communication skills to present and explain the methodology and consequences of decisions.

The Senior External Data Specialist (SEDS) is responsible for providing technical, procedural (SOPs) and planning leadership across multiple projects assigned to the external data group team members ensuring that they deliver in accordance with SOPs, programming best practices, and the timelines agreed within the Project Team. Scope external study data requirements and effort for projects. Project manage all external data related activities across multiple projects. Provide expert advice on the transfer and expected formats of data transfer files. Provide technological expertise and guidance on the best methods for handling laboratory data and other external data. Create and maintain data transfer agreements. Maintain study documentation within project files as appropriate. Act as primary contact and study representative to third party data providers. Effectively communicate transfer requirements and project timelines to various stakeholders. Identify and communicate project risks. Ensure data integrity is maintained by implementing appropriate data controls for masked data. Ensure delivery of timely data transfers and undertake quality reviews and testing activities. Conduct external data reconciliation using available technologies and processes. Raise queries to external data providers and track queries to successful resolution. Provide listings to medical review team. Assess and implement new data review and analysis processes and technologies. Take a lead role in the development of best practices, process improvement, quality control and governance related to all external data matters. Provide training and mentoring to team members in SOPs, software applications, and best practices. Attributes and Skills-Expert domain knowledge and experience within clinical research and drug development. Advanced knowledge in >1 EDC systems and laboratory processes. Experience mentoring and training others. Awareness of regulatory and compliance issues and understanding of application of SOPs and Quality Control to daily activities. Excellent analytical, communication and problem-solving skills. Responsibilities The Senior External Data Specialist (SEDS) is responsible for providing technical, procedural (SOPs) and planning leadership across multiple projects assigned to the external data group team members ensuring that they deliver in accordance with SOPs, programming best practices, and the timelines agreed within the Project Team. Scope external study data requirements and effort for projects. Project manage all external data related activities across multiple projects. Provide expert advice on the transfer and expected formats of data transfer files. Provide technological expertise and guidance on the best methods for handling laboratory data and other external data. Create and maintain data transfer agreements. Maintain study documentation within project files as appropriate. Act as primary contact and study representative to third party data providers. Effectively communicate transfer requirements and project timelines to various stakeholders. Identify and communicate project risks. Ensure data integrity is maintained by implementing appropriate data controls for masked data. Ensure delivery of timely data transfers and undertake quality reviews and testing activities. Conduct external data reconciliation using available technologies and processes. Raise queries to external data providers and track queries to successful resolution. Provide listings to medical review team. Assess and implement new data review and analysis processes and technologies. Take a lead role in the development of best practices, process improvement, quality control and governance related to all external data matters. Provide training and mentoring to team members in SOPs, software applications, and best practices. Attributes and Skills Expert domain knowledge and experience within clinical research and drug development. Advanced knowledge in >1 EDC systems and laboratory processes. Experience mentoring and training others. Awareness of regulatory and compliance issues and understanding of application of SOPs and Quality Control to daily activities. Excellent analytical, communication and problem-solving skills.

The role holder is responsible for contributing to the discovery and pre-development of innovative solutions in agrochemistry, namely new a.i.s for crop protection adding significant value to the business of PI. The role will to carry out literature/patent search, FTO analysis and other KM services in accordance with the project timelines and objectives. The role holder will plan and propose to Group Leader - KM all input, equipment and other requirements for approval and procurement to ensure efficient conduct of project activities and contribute to generating IP and ensuring it s protection Strategic Responsibilities Efficient contribution to the overall success of CreAgro by driving innovation and team performance according to objectives and targets being set by the Director of Knowledge Management Generating and ensuring the security of intellectual property for CreAgro (filing of patent applications, building and defending the PI patent portfolio, ensuring novelty and freedom-to-operate) Promoting knowledge sharing through the organization, strengthening links between KM and CreAgro chemistry/biology teams Foster collaboration with customers and external partners Continuously build knowledge on the area of agro-chemistry and KM specific expertise, through active learning, education, advanced trainings and seminars Support GL KM with special focus on target setting, development of strengths, building of knowhow, feedback and coaching Operational Responsibilities Keep self and team updated on the state of the art in IP management and KM specific tools Carrying KM services like FTO analysis and opinion, novelty search, literature supply and others with appropriate documentation and distribution of results Support competitor intelligence activities Develop and foster positive relationships with other teams and support groups such as chemistry/biology to maximize knowledge sharing and cooperation Comply with all the safety requirements as per the requirement of the role Leading knowledge transfer through presentations, training materials, tips and best practices for collaboration, so as to continually improve the performance of the group Financial Responsibilities Contribute to budget proposals Contributes to budgetary controls within the area of responsibility People Responsibilities Act as a committed ambassador of PI Brand Actively imbibing the values and philosophy of PI Industries Ltd. Ensure smooth working by maintaining high level of morale and working ethics Education Qualification MSc/PhD in chemistry (organic) from a reputed university/ institute/group Work Experience Post-doctoral research experience in a reputed university is desirable Post academic industrial research experience of > 2 years in new a.i. discovery in pharma and/or crop protection OR Post academic experience of > 2 years in the area of IP in pharma and/or crop protection Substantial number of high quality research publications and/or patents Experimental skills and expert knowledge concerning synthesis, analysis and characterisation of organic molecules related areas appreciated Knowledge and practical experience concerning patent analysis (FTO, novelty) Industry to be Hired from Agro/pharma /chemical industries Functional Competencies Technical Knowledge Data Analysis

Designation: Home Loan Officer (Sales) at HDFC Sales. Job location:- Bangalore, Hyderabad, Chennai. Department : Home Loan ( Sales) Qualification:- Any Graduation / Post-graduation. Experience: 0 to 1 Years CTC: - 1.80 lpa to 2.50 lpa + Huge Incentive ( Upto 50000 ) Roles & Responsibilities:- Area/ Lane /Geography Mapping: Responsible for lane to lane/ Area mapping of Area/ Geography at regular intervals with the help of supervisor. Identify new sources in the allocated Area/ Geography and inform the progress to reporting manager during team huddle. Source Relationship Management: Responsible for managing the relationship with all sources assigned and identified by him in his geography/area. Maintain Reports: Responsible for maintaining reports related to sales and all his activities in the prescribed format. Should maintain diary on daily basis in the prescribed format of activities. Channel Partner Recruitment: Responsible for identifying the need for appointment of a channel partner Team Huddle: Responsible for attending team huddle on a daily basis as per the set process. Customer Relationship Management: Responsible for enhancing the customer experience by developing and maintaining relationship with customers. Completion of File: Responsible for submission of complete application form, documentations and information. Desired candidate profile: Must be a graduate from any stream Should have minimum 6 months of experience in sales Candidates with prior experience in BFSI will have an added advantage Open to travel Must have good communication skills For further Details, contact- aykacommunication28@gmail.com Note: Candidates should be flexible with field work. Contact HR. 8105002838 (Call or WhatsApp) 7829353208 (Call or WhatsApp)

The position will be responsible for development of assigned project within given timeframe as per safety and environmental rules. This includes thorough literature survey, bench scale trials, preparation of SOPs, necessary documentation. This would also include Demo of developed chemical process to PD team, support in KL, pilot plant and commercial plant for successful technology transfer. Strategic Responsibilities To understand the objective of project / chemistry / MSDS Search the additional literature as required. Inputs in planning of experiments/ man power / glassware/ raw materials/ analysis To ensure proper maintenance of lab equipment s. Proper house- keeping and use of PPE s. Use relevant MSDS for safe handling and disposals of toxic chemicals Operational Responsibilities Bench scale experiments as per planning and Identification of critical parameters Co-ordination with QC for analytical support / development and Prepare sample as per required quality Optimization of process w.r.t. identified critical parameters and Impurities characterization and synthesis. Understanding the parameters responsible for impurities. Process validation by reproducing min. three consecutive batches. Experimental observations and data compilation Demo batches to PD To check quality plan/ Plant SOP and Use test of RM s Data compilation and time to time update of KL/ PP plant trials Financial Responsibilities Contribute to budget proposals. Contribute to budgetary controls within the area of responsibility. People Responsibilities Utilization of all available sources for skill up-gradation Actively participation in problem solving sessions/ training programs Coordination and communication with team To guide subordinates Education Qualification Master and PhD in Organic Chemistry from a reputed University / Institute Work Experience 0-8 years of Industrial Experience. Industry to be Hired from Agro chemicals/fine chemicals/ pharma-API/ Specialty chemicals. Functional Competencies Route Scouting Literature Search Practical Experience of Lab working Understanding of HSE Data Management Analytical data interpretation

The Position will be responsible for development of assigned project within given timeframe using new Technology. This includes thorough literature survey, bench scale trials, preparation of SOPs, necessary documentation. This would also include Demo of developed chemical process to PD team, support in KL, pilot plant and commercial plant for successful technology transfer. Strategic Responsibilities To understand the objective of project / chemistry / MSDS Search the additional literature as required. Inputs in planning of experiments/ glassware/ raw materials/ analysis To ensure proper maintenance of lab equipments. Proper house- keeping and use of PPE s. Use relevant MSDS for safe handling and disposals of toxic chemicals Operational Responsibilities Development of processes using flow chemistry (Micro /Meso reactors). Mapping the suitable reactor & pumps for development of process in Flow Technology Finding out suitable equipment for downstream operation for continuous manufacturing. To generate data for carrying out scale-up study using Design of Experiment mechanism To ensure seamless efficient scale-up of the process developed by working closely with Process Chemist team. To identify the cost reduction opportunities in the projects already running at commercial scale using flow technology. Drive optimum utilization of all available resources Financial Responsibilities Actively participate in problem solving sessions/ training programs and drive coordination and communication within the team Ensure on time delivery of assigned project in terms of: On time delivery with target yield and quality. Waste minimization Smooth scale-up up to KL/PP Ensuring the safety & house keeping Inspire & motivate employees through demonstrated commitment to PI s values, vision & mission and exemplifying effective leadership, initiative and persistence needed to accomplish goals and objectives Drive collaboration and cross-functional networking for the entire team People Responsibilities Foster an environment of knowledge sharing within the Team Maintain healthy working relationships with the related teams and departments. Education Qualification Master/Doctorate in Organic Chemistry from a reputed University / Institute Work Experience 0-8 Industrial Experience. Industry to be Hired from Agro chemicals/fine chemicals/ pharma-API/ Specialty chemicals Functional Competencies Experience in Flow Chemistry/Technology Practical Experience working on Flow reactors (Static and Dynamic) Experience in handling different types of Pumps Documentation, report writing and familiar with MS office suite Data Management Analytical data interpretation

Designation: Relationship Executive/Relationship Officer for HDB Finance . Job location:- Hyderabad , Bangalore & Chennai.(Male) Note :- Near by Branch to your location Department:-Current Account, Saving Account, Home Loan / Auto Loan / Loan Against Property / Business Loan/ Auto Loan, Commercial Vehicle/ Credit Card/ Persional Loan. Qualification:- Any Graduation / Post-graduation. CTC : - 12 K +16 K Huge Incentive ( Upto 50000 ) Exp : - 0 to 3 Year(Fresher can also apply) Age : - 18 to 34 Job Description:- Demonstrating/ Presenting/ Introducing/ Selling banking products of the client. New client acquisition Convincing customer for new product and maintaining relationship with clients Responsible for processing/ documentations of Loans & other financial services Create and drive alternate channels for business along with the regular channels Open up avenues for business through corporate channel. Analyzing of business trends and target figures to formulate new For further Details, contact- aykacommunication28@gmail.com Note: Candidates should be flexible with field work. Perks and Benefits Perks and Benefits Incentives Contact HR 8105002838 (Call or WhatsApp) 7829353208 (Call or WhatsApp)

* Identify and approach potential customers. * Persuade customers to purchase product or services. * Achieve Set sales goals and quotas. * Build and Nurture customer relationship for repeat business. * Provide regular activity on sales performance Required Candidate profile Any sales exp. of 2 years Graduation should be completed Must be local Age - 24 to 39 Last company documents mandatory Should be ready for Hard core sales Sr. HR Neha (8488981861) Perks and benefits On Role Job + High CTC Allowances + Incentives