162 Radiopharmaceuticals Jobs

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products, and Generics & APIs, comprising Solid Dosage Formulations & Active Pharmaceutical Ingredients. Jubilant Generics (JGL) is a wholly - owned subsidiary of Jubilant Pharma. JGL in India has Research & Development units at Noida and Mysore. It has two manufacturing facilities one at Mysore, Karnataka and another at Roorkee, Uttarakhand, engaged in APIs and Dosage manufacturing, respectively. The manufacturing location at Mysore is spread over 69 acres and it’s a USFDA approved site engaged in manufacturing of APIs, and caters to the sales worldwide. API portfolio focusses on Lifestyle driven Therapeutic Areas (CVS, CNS) and targets complex and newly approved molecules. The company is the market leader in four APIs and is amongst the top three players for another three APIs in its portfolio helping it maintain a high contribution margin. The manufacturing location at Roorkee, Uttarakhand is state of the art facility and is audited and approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA. This business focusses on B2B model for EU, Canada and emerging markets. Both manufacturing units are backward- integrated and are supported by around 500 research and development professionals based at Noida and Mysore. R&D works on Development of new products in API, Solid Dosage Formulations of Oral Solid, Sterile Injectable, Semi-Solids Ointments, Creams and Liquids. All BA/BE studies are done In house at our 80 Bed facility which is inspected and having approvals /certifications from The Drugs Controller General (India) and has global regulatory accreditations including USFDA, EMEA, ANVISA (Brazil), INFRAMED (Portugal Authority), NPRA(Malaysia), AGES MEA (Austria) for GCP and NABL, CAP accreditations for Path lab services. JGL’s full-fledged Regulatory Affairs & IPR professionals ensures unique portfolio of patents and product filings in regulatory and non-regulatory market. Revenue of Jubilant Pharma is constantly increasing and during the Financial Year 2018 -19 it was INR 53,240 Million as compared to INR 39,950 Million during the Financial Year 2017-18. Kindly refer www.jubilantpharma.com for more information about organization.

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products, and Generics & APIs, comprising Solid Dosage Formulations & Active Pharmaceutical Ingredients. Jubilant Generics (JGL) is a wholly - owned subsidiary of Jubilant Pharma. JGL in India has Research & Development units at Noida and Mysore. It has two manufacturing facilities one at Mysore, Karnataka and another at Roorkee, Uttarakhand, engaged in APIs and Dosage manufacturing, respectively. The manufacturing location at Mysore is spread over 69 acres and it’s a USFDA approved site engaged in manufacturing of APIs, and caters to the sales worldwide. API portfolio focusses on Lifestyle driven Therapeutic Areas (CVS, CNS) and targets complex and newly approved molecules. The company is the market leader in four APIs and is amongst the top three players for another three APIs in its portfolio helping it maintain a high contribution margin. The manufacturing location at Roorkee, Uttarakhand is state of the art facility and is audited and approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA. This business focusses on B2B model for EU, Canada and emerging markets. Both manufacturing units are backward- integrated and are supported by around 500 research and development professionals based at Noida and Mysore. R&D works on Development of new products in API, Solid Dosage Formulations of Oral Solid, Sterile Injectable, Semi-Solids Ointments, Creams and Liquids. All BA/BE studies are done In house at our 80 Bed facility which is inspected and having approvals /certifications from The Drugs Controller General (India) and has global regulatory accreditations including USFDA, EMEA, ANVISA (Brazil), INFRAMED (Portugal Authority), NPRA(Malaysia), AGES MEA (Austria) for GCP and NABL, CAP accreditations for Path lab services. JGL’s full-fledged Regulatory Affairs & IPR professionals ensures unique portfolio of patents and product filings in regulatory and non-regulatory market. Revenue of Jubilant Pharma is constantly increasing and during the Financial Year 2018 -19 it was INR 53,240 Million as compared to INR 39,950 Million during the Financial Year 2017-18. Kindly refer www.jubilantpharma.com for more information about organization.

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products, and Generics & APIs, comprising Solid Dosage Formulations & Active Pharmaceutical Ingredients. Jubilant Generics (JGL) is a wholly - owned subsidiary of Jubilant Pharma. JGL in India has Research & Development units at Noida and Mysore. It has two manufacturing facilities one at Mysore, Karnataka and another at Roorkee, Uttarakhand, engaged in APIs and Dosage manufacturing, respectively. The manufacturing location at Mysore is spread over 69 acres and it’s a USFDA approved site engaged in manufacturing of APIs, and caters to the sales worldwide. API portfolio focusses on Lifestyle driven Therapeutic Areas (CVS, CNS) and targets complex and newly approved molecules. The company is the market leader in four APIs and is amongst the top three players for another three APIs in its portfolio helping it maintain a high contribution margin. The manufacturing location at Roorkee, Uttarakhand is state of the art facility and is audited and approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA. This business focusses on B2B model for EU, Canada and emerging markets. Both manufacturing units are backward- integrated and are supported by around 500 research and development professionals based at Noida and Mysore. R&D works on Development of new products in API, Solid Dosage Formulations of Oral Solid, Sterile Injectable, Semi-Solids Ointments, Creams and Liquids. All BA/BE studies are done In house at our 80 Bed facility which is inspected and having approvals /certifications from The Drugs Controller General (India) and has global regulatory accreditations including USFDA, EMEA, ANVISA (Brazil), INFRAMED (Portugal Authority), NPRA(Malaysia), AGES MEA (Austria) for GCP and NABL, CAP accreditations for Path lab services. JGL’s full-fledged Regulatory Affairs & IPR professionals ensures unique portfolio of patents and product filings in regulatory and non-regulatory market. Revenue of Jubilant Pharma is constantly increasing and during the Financial Year 2018 -19 it was INR 53,240 Million as compared to INR 39,950 Million during the Financial Year 2017-18. Kindly refer www.jubilantpharma.com for more information about organization.

We’re Hiring : Head of Digital & Information Technology (DIT), Pharmova India (Sr. Director/ AVP Level) Location : Bengaluru Organization : Jubilant Pharmova Limited (Part of the Jubilant Bhartia Group) At Jubilant Bhartia Group , we believe in driving growth through innovation, transformation, and excellence. With a global workforce of 43,000+ across Pharmaceuticals, Life Sciences, Food Services, Consulting, and more — we are shaping the future every day. About Jubilant Pharmova Limited An integrated global pharmaceutical company focused on: - Radiopharmaceuticals & Allergy Therapy Products - Contract Manufacturing (Sterile & Non-Sterile) - APIs & Solid Dosage Formulations - Collaborative R&D and Novel Drug Discovery The Opportunity As Head DIT (Sr.Director), you will be the IT leader for Pharmova India — defining and executing the digital roadmap, driving AI/GenAI initiatives, and enabling business transformation across R&D, Manufacturing, Quality, Regulatory, and Commercial functions. Key Impact Areas: - Shape and implement Pharmova’s Digital & IT Strategy - Champion digital transformation and cutting-edge AI/GenAI interventions - Ensure robust IT governance, cybersecurity, and regulatory (GxP) compliance - Deliver high-impact projects on time, within cost, and with measurable value - Build, lead, and inspire a high-performance IT team What We’re Looking For: - 15–20 years’ experience in IT leadership across complex enterprises - Proven expertise in digital transformation, program management, and solution delivery - Strong exposure to Pharma/CRDMO industries with GxP/regulatory knowledge (preferred) - Strategic thinker with strong execution and stakeholder engagement skills Why Join Us? At Jubilant Pharmova, you’ll have the platform to: - Lead digital transformation in a global pharma enterprise - Work with senior leadership on strategic initiatives - Deliver innovations that directly impact healthcare outcomes If you are a visionary IT leader ready to drive transformation, we invite you to apply. 🔗 Learn more: www.jubilantpharmova.com To apply, please share your profile at [usha.dhoundiyal@jepl.com]

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products, and Generics & APIs, comprising Solid Dosage Formulations & Active Pharmaceutical Ingredients. Jubilant Generics (JGL) is a wholly - owned subsidiary of Jubilant Pharma. JGL in India has Research & Development units at Noida and Mysore. It has two manufacturing facilities one at Mysore, Karnataka and another at Roorkee, Uttarakhand, engaged in APIs and Dosage manufacturing, respectively. The manufacturing location at Mysore is spread over 69 acres and it’s a USFDA approved site engaged in manufacturing of APIs, and caters to the sales worldwide. API portfolio focusses on Lifestyle driven Therapeutic Areas (CVS, CNS) and targets complex and newly approved molecules. The company is the market leader in four APIs and is amongst the top three players for another three APIs in its portfolio helping it maintain a high contribution margin. The manufacturing location at Roorkee, Uttarakhand is state of the art facility and is audited and approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA. This business focusses on B2B model for EU, Canada and emerging markets. Both manufacturing units are backward- integrated and are supported by around 500 research and development professionals based at Noida and Mysore. R&D works on Development of new products in API, Solid Dosage Formulations of Oral Solid, Sterile Injectable, Semi-Solids Ointments, Creams and Liquids. All BA/BE studies are done In house at our 80 Bed facility which is inspected and having approvals /certifications from The Drugs Controller General (India) and has global regulatory accreditations including USFDA, EMEA, ANVISA (Brazil), INFRAMED (Portugal Authority), NPRA(Malaysia), AGES MEA (Austria) for GCP and NABL, CAP accreditations for Path lab services. JGL’s full-fledged Regulatory Affairs & IPR professionals ensures unique portfolio of patents and product filings in regulatory and non-regulatory market. Revenue of Jubilant Pharma is constantly increasing and during the Financial Year 2018 -19 it was INR 53,240 Million as compared to INR 39,950 Million during the Financial Year 2017-18. Kindly refer www.jubilantpharma.com for more information about organization.

Job Description Completing the patients’ intake process, taking patients’ histories, and preparing and educating patients about the imaging procedure. Reviewing patients’ charts and Doctors’ notes before the examination, and maintaining patients’ records during and after procedures. Preparing radiopharmaceuticals for contrast in the diagnostic images. Positioning patients and equipment to capture the correct area and produce clear images. Monitoring patients and ensuring their safety during imaging procedures. Calibrating the equipment to ensure clear, usable images are taken of the correct area, as specified by the Doctor. Experience - X-Ray & CT Salary - 10k To 12K On duty food & Accommodation facility. Job Types: Full-time, Permanent Pay: ₹10,000.00 - ₹12,000.00 per month Benefits: Food provided Provident Fund Work Location: In person

Company Description Cancer Centers of America (CCA) is a comprehensive oncology platform designed to provide accessible and affordable world-class cancer care. Our mission is to ensure that patients receive the highest quality of care, tailored to their specific needs and conditions. CCA integrates the latest medical advancements and compassionate care to offer a wide range of oncology services. Role Description This is a full-time, on-site role for a Nuclear Medicine Technologist Cum RSO 2 located in Nashik. The role includes responsibilities such as preparing and administering radiopharmaceuticals, performing diagnostic imaging procedures, ensuring radiation safety in compliance with regulations, and maintaining detailed patient records. The technologist will also assist in patient care, collaborate with other healthcare professionals, and operate imaging equipment safely and effectively. Qualifications Proficiency in preparing and administering radiopharmaceuticals and performing diagnostic imaging procedures Strong understanding of radiation safety protocols and regulatory compliance Skills in maintaining detailed patient records and documentation Excellent communication and teamwork abilities Certification as a Nuclear Medicine Technologist Experience as a Radiation Safety Officer (RSO) is an advantage Relevant bachelor's degree in Nuclear Medicine Technology or a related field

Radiographer Key Responsibilities Operating imaging equipment: Radiographers operate various imaging devices, including X-ray machines, CT scanners, and MRI machines, to capture images of the body. Positioning patients: They accurately position patients for imaging procedures to ensure optimal image quality and minimize radiation exposure. Ensuring patient safety: They prioritize patient safety by monitoring patients during procedures, administering medications (if needed), and ensuring proper radiation protection. Maintaining patient records: Radiographers maintain accurate records of patient imaging procedures, including patient demographics, imaging parameters, and image results. Assisting with imaging procedures: They assist with various imaging procedures, such as fluoroscopy (real-time X-ray imaging), contrast studies (using dyes to enhance images), and specialized imaging techniques. Collaborating with other healthcare professionals: Radiographers work closely with radiologists, doctors, nurses, and other healthcare professionals to ensure the best possible patient care. Specific Tasks May Include: Preparing patients for imaging procedures, explaining the process, and addressing their concerns. Calibrating and maintaining imaging equipment. Preparing and administering radiopharmaceuticals for contrast studies. Ensuring proper sterilization of equipment. Assisting with the development and implementation of new protocols and procedures. Ensuring radiation safety protocols are followed. May assist with the interpretation of radiograph results. Additional Notes: Radiographers typically work in hospitals, clinics, and diagnostic imaging centers. They may work fixed shifts, including evenings, weekends, and holidays. The role requires a combination of technical skills, knowledge of anatomy and physiology, and strong communication skills. Radiographers play a crucial role in the accurate diagnosis and treatment of a wide range of medical conditions Qualification: BSC from approved universities Diploma under DME Job Type: Full-time Pay: ₹15,000.00 - ₹25,000.00 per month Benefits: Provident Fund Education: Master's (Required) Experience: 5years: 2 years (Required) Language: English (Preferred) Work Location: In person

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products, and Generics & APIs, comprising Solid Dosage Formulations & Active Pharmaceutical Ingredients. Jubilant Generics (JGL) is a wholly - owned subsidiary of Jubilant Pharma. JGL in India has Research & Development units at Noida and Mysore. It has two manufacturing facilities one at Mysore, Karnataka and another at Roorkee, Uttarakhand, engaged in APIs and Dosage manufacturing, respectively. The manufacturing location at Mysore is spread over 69 acres and it’s a USFDA approved site engaged in manufacturing of APIs, and caters to the sales worldwide. API portfolio focusses on Lifestyle driven Therapeutic Areas (CVS, CNS) and targets complex and newly approved molecules. The company is the market leader in four APIs and is amongst the top three players for another three APIs in its portfolio helping it maintain a high contribution margin. The manufacturing location at Roorkee, Uttarakhand is state of the art facility and is audited and approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA. This business focusses on B2B model for EU, Canada and emerging markets. Both manufacturing units are backward- integrated and are supported by around 500 research and development professionals based at Noida and Mysore. R&D works on Development of new products in API, Solid Dosage Formulations of Oral Solid, Sterile Injectable, Semi-Solids Ointments, Creams and Liquids. All BA/BE studies are done In house at our 80 Bed facility which is inspected and having approvals /certifications from The Drugs Controller General (India) and has global regulatory accreditations including USFDA, EMEA, ANVISA (Brazil), INFRAMED (Portugal Authority), NPRA(Malaysia), AGES MEA (Austria) for GCP and NABL, CAP accreditations for Path lab services. JGL’s full-fledged Regulatory Affairs & IPR professionals ensures unique portfolio of patents and product filings in regulatory and non-regulatory market. Revenue of Jubilant Pharma is constantly increasing and during the Financial Year 2018 -19 it was INR 53,240 Million as compared to INR 39,950 Million during the Financial Year 2017-18. Kindly refer www.jubilantpharma.com for more information about organization. Scope of the role Scope - This role is responsible for Responsibilities – Supervision & Control Managing Team Brand growth Prescription Growth Prescribers growth Market Share Ensuring ROI Development of subordinates Relationships around the role Reporting to (Business) Zonal Sales Manager Reporting to (Matrix) NA No of Reportees Direct 4-5 Indirect NA Key External Stakeholder(s) Doctors, Stockiest, Retailers, CFA staff, Fellow professionals, Institutional administrators Key Internal Stakeholder(s) Superiors, Subordinates , PMT, HR & Sales Admin Competencies critical for the role Scientific/ Technical Competencies Proficiency level Proven Leadership qualities Good communicator Proven track records Ambitious Behavioral Analytical ability PR Skills Dependable Contributor Good Products knowledge Creative & Assertive Qualifications Academic qualifications and experience required for the role Required Educational Qualification & Relevant experience Desirable - B.Pharm / D.Pharm / BSc. + MBA Essential - Graduates in any discipline Experience : 5 to 7 years of Total experience and 1 – 2 years of First Line experience Age should be around 32 years

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products, and Generics & APIs, comprising Solid Dosage Formulations & Active Pharmaceutical Ingredients. Jubilant Generics (JGL) is a wholly - owned subsidiary of Jubilant Pharma. JGL in India has Research & Development units at Noida and Mysore. It has two manufacturing facilities one at Mysore, Karnataka and another at Roorkee, Uttarakhand, engaged in APIs and Dosage manufacturing, respectively. The manufacturing location at Mysore is spread over 69 acres and it’s a USFDA approved site engaged in manufacturing of APIs, and caters to the sales worldwide. API portfolio focusses on Lifestyle driven Therapeutic Areas (CVS, CNS) and targets complex and newly approved molecules. The company is the market leader in four APIs and is amongst the top three players for another three APIs in its portfolio helping it maintain a high contribution margin. The manufacturing location at Roorkee, Uttarakhand is state of the art facility and is audited and approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA. This business focusses on B2B model for EU, Canada and emerging markets. Both manufacturing units are backward- integrated and are supported by around 500 research and development professionals based at Noida and Mysore. R&D works on Development of new products in API, Solid Dosage Formulations of Oral Solid, Sterile Injectable, Semi-Solids Ointments, Creams and Liquids. All BA/BE studies are done In house at our 80 Bed facility which is inspected and having approvals /certifications from The Drugs Controller General (India) and has global regulatory accreditations including USFDA, EMEA, ANVISA (Brazil), INFRAMED (Portugal Authority), NPRA(Malaysia), AGES MEA (Austria) for GCP and NABL, CAP accreditations for Path lab services. JGL’s full-fledged Regulatory Affairs & IPR professionals ensures unique portfolio of patents and product filings in regulatory and non-regulatory market. Revenue of Jubilant Pharma is constantly increasing and during the Financial Year 2018 -19 it was INR 53,240 Million as compared to INR 39,950 Million during the Financial Year 2017-18. Kindly refer www.jubilantpharma.com for more information about organization. Scope of the role Scope - This role is responsible for Responsibilities – Supervision & Control Managing Team Brand growth Prescription Growth Prescribers growth Market Share Ensuring ROI Development of subordinates Relationships around the role Reporting to (Business) Zonal Sales Manager Reporting to (Matrix) NA No of Reportees Direct 4-5 Indirect NA Key External Stakeholder(s) Doctors, Stockiest, Retailers, CFA staff, Fellow professionals, Institutional administrators Key Internal Stakeholder(s) Superiors, Subordinates , PMT, HR & Sales Admin Competencies critical for the role Scientific/ Technical Competencies Proficiency level Proven Leadership qualities Good communicator Proven track records Ambitious Behavioral Analytical ability PR Skills Dependable Contributor Good Products knowledge Creative & Assertive Qualifications Academic qualifications and experience required for the role Required Educational Qualification & Relevant experience Desirable - B.Pharm / D.Pharm / BSc. + MBA Essential - Graduates in any discipline Experience : 5 to 7 years of Total experience and 1 – 2 years of First Line experience Age should be around 32 years

Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. Jubilant Pharmova Limited Jubilant Pharmova Limited (formerly Jubilant Life Sciences Limited) is a company with global presence that is involved in Radiopharma, Allergy Immunotherapy, CDMO Sterile Injectables, Contract Research Development and Manufacturing Organisation (CRDMO), Generics and Proprietary Novel Drugs businesses. In the Radiopharma business, the Company is involved in manufacturing and supply of Radiopharmaceuticals with a network of 46 radio-pharmacies in the US. The Company’s Allergy Immunotherapy business is involved in the manufacturing and supply of allergic extracts and venom products in the US and in some other markets such as Canada, Europe and Australia. Jubilant through its CDMO Sterile Injectables business offers manufacturing services including sterile fill and finish injectables (both liquid and lyophilization), full-service ophthalmic offer (liquids, ointments & creams) and ampoules. The CRDMO business of the Company includes the Drug Discovery Services business that provides contract research and development services through two world-class research centres in Bangalore and Noida in India and the CDMO-API business that is involved in the manufacturing of Active Pharmaceutical Ingredients. Jubilant Therapeutics is involved in Proprietary Novel Drugs business and is an innovative biopharmaceutical company developing breakthrough therapies in the area of oncology and autoimmune disorders. The company operates six manufacturing facilities that cater to all the regulated market including USA, Europe and other geographies. The Position Organization- Jubilant Pharmova Limited Designation - Dy Manager- SAP Location- Noida Job Summary: The role plays a pivotal role in the end-to-end implementation, configuration, and optimization of SAP SuccessFactors modules, bridges the gap between business needs and technical solutions, ensuring seamless integration and functionality across systems. Collaborate for driving the technical architecture and integration strategy across SuccessFactors modules, ensuring the delivery of scalable, secure, and high-performance solutions that align with organizational objectives. Responsibilities Key Responsibilities. Define and maintain the overall architecture of SAP SuccessFactors solutions. Lead end-to-end implementations across multiple modules (e.g., Employee Central, Performance & Goals, Learning, Recruiting). Collaborate with implementation team and business stakeholders to translate requirements into technical solutions. Coordinate with external implementation partners to ensure alignment with architectural standards and project timelines. Review and validate technical deliverables from partners to ensure quality and compliance. Act as the primary technical point of contact between internal teams and implementation vendors. Design and develop custom solutions using SAP BTP, Integration Centre, and APIs. Manage middleware integrations (e.g., SAP CPI, Dell Boomi, MuleSoft) with third-party systems. Ensure data consistency and synchronization across systems. Oversee ongoing support and enhancements of SuccessFactors modules. Troubleshoot and resolve technical issues, ensuring minimal disruption to business operations. Monitor system performance and implement optimization strategies. Establish and enforce development standards, security protocols, and documentation practices. Stay updated with SAP SuccessFactors releases and innovations, recommending adoption strategies. Person Profile . Qualification - Bachelor’s / Master’s degree in Technology or related field. Experience – 8 -10 years of relevant experience proven experience in managing implementations across diverse geographies, including India, US, and Canada. SAP SuccessFactors certifications in Employee Central (EC) and Payroll are highly desirable and will be considered a strong advantage . Desired Certification & Must Have- IT Project & Program Management skills Vendor Management Excellent written and verbal communication skills Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances

Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. Jubilant Pharmova Limited Jubilant Pharmova Limited (formerly Jubilant Life Sciences Limited) is a company with global presence that is involved in Radiopharma, Allergy Immunotherapy, CDMO Sterile Injectables, Contract Research Development and Manufacturing Organisation (CRDMO), Generics and Proprietary Novel Drugs businesses. In the Radiopharma business, the Company is involved in manufacturing and supply of Radiopharmaceuticals with a network of 46 radio-pharmacies in the US. The Company’s Allergy Immunotherapy business is involved in the manufacturing and supply of allergic extracts and venom products in the US and in some other markets such as Canada, Europe and Australia. Jubilant through its CDMO Sterile Injectables business offers manufacturing services including sterile fill and finish injectables (both liquid and lyophilization), full-service ophthalmic offer (liquids, ointments & creams) and ampoules. The CRDMO business of the Company includes the Drug Discovery Services business that provides contract research and development services through two world-class research centres in Bangalore and Noida in India and the CDMO-API business that is involved in the manufacturing of Active Pharmaceutical Ingredients. Jubilant Therapeutics is involved in Proprietary Novel Drugs business and is an innovative biopharmaceutical company developing breakthrough therapies in the area of oncology and autoimmune disorders. The company operates six manufacturing facilities that cater to all the regulated market including USA, Europe and other geographies. The Position Organization- Jubilant Pharmova Limited Designation - Data Scientist Location- Noida Job Summary: The role plays a Plays a crucial role in helping businesses make informed decisions by leveraging data & Advanced AI Solutions & will collaborate with stakeholders, design data models, create algorithms, and share meaningful insights to drive business success Key Responsibilities- Data & Analytics Work with supply chain, manufacturing manager, warehouse managers, customer account managers and quality function to produce manufacturing schedules, solutions to improve existing processes Gathering and interpreting data from various sources. Cleaning and verifying the accuracy of data sets to ensure data integrity. Build and maintain data pipelines for collecting, preprocessing, and integrating diverse data sources for comprehensive analysis and actionable insights. Developing and implementing data collection systems and strategies to optimize efficiency and accuracy. Applying statistical techniques to analyse and interpret complex data sets. Develop and implement statistical models for predictive analysis. Build and deploy machine learning models to solve business problems. Creating visual representations of data through charts, graphs, and dashboards to communicate findings effectively. Develop dashboards and reports for ongoing monitoring and analysis. Create, modify and improve complex manufacturing schedule. Create scenario planning model for manufacturing. Develop manufacturing schedule adherence probability model. Regularly monitoring and evaluating data quality, making recommendations for improvements as necessary. Staying up-to-date with industry trends and best practices in data analysis and reporting. Ensuring compliance with data privacy and security regulations. Key Responsibilities- AI End-to-End AI Solution Development Data Engineering: Independently develop data pipelines, perform data extraction, transformation, and loading (ETL) for AI model consumption. Model Integration : Integrate foundational models and retrieval-augmented generation (RAG) techniques Backend Development: Implement backend services and API endpoints to support AI solutions. Frontend Integration : Develop or adapt frontend interfaces for user interaction. Innovation & Self-Development Continuous Learning: Stay current on foundational AI models, RAG techniques Ownership & Autonomy : Take full ownership of assigned use cases, handling all aspects of development, testing, and deployment with minimal supervision Person Profile. Qualification- B. Tech- CSE,ECE. Experience - 3-5 years of relevant experience in preferably Pharma/Chemical/Manufacturing Industry. Technical Skills - Preferred P rogramming : Proficiency in Python for data handling and AI-related scripting. Data Engineering: Familiarity with data pipeline development, ETL processes, and data preprocessing techniques. Testing and QA : Knowledge of testing frameworks and tools to ensure model robustness, as well as experience with automated testing for QA processes. Other Skills- Preferred Experience with RAG : Familiarity with Retrieval-Augmented Generation techniques and their applications. Prompt Engineering : Knowledge of prompt engineering techniques to optimize generative AI models for specific tasks and enhance output relevance. Predictive Modelling : Experience in predictive modeling areas, such as traditional supervised and unsupervised learning, Advanced AI Concepts : Basic familiarity with foundational generative AI models and Natural Language Processing (NLP). Experience with big data technologies (e.g., Hadoop, Spark). Knowledge of cloud platforms (e.g., AWS, Azure, Google Cloud). Strong analytical and problem-solving skills with the ability to handle complex data sets. Excellent attention to detail and a high level of accuracy in data analysis. Solid knowledge of data visualization techniques and experience using visualization tools like Tableau or Power BI. Strong communication skills to present findings and insights to non-technical stakeholders effectively Ability to work collaboratively in a team environment and adapt to changing priorities. Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances.

Company Description Mahatma Gandhi Cancer Hospital and Research Institute, located in MVP Colony, Visakhapatnam, Andhra Pradesh, India, is one of the largest cancer centers in the country. MGCH & RI provides comprehensive cancer care and prevention under one roof through diagnostics, advanced therapies like Surgery, Chemotherapy, Radiotherapy, and symptom management. The Institute is focused on a patient-centered approach to improving quality of life and restoring hope with compassionate care in a comfortable and friendly environment. Role Description This is a full-time on-site role for a Nuclear Medicine Technologist located in Visakhapatnam. The Nuclear Medicine Technologist will be responsible for preparing and administering radiopharmaceuticals, performing nuclear medicine procedures, ensuring patient safety regarding radiation exposure, and adhering to radiation safety protocols. The role includes maintaining imaging equipment, preparing diagnostic reports, and collaborating with medical professionals to interpret imaging results. Qualifications Proficiency in Nuclear Medicine and Radiopharmaceuticals Skills in Radiation Safety and ensuring compliance with safety standards Strong understanding of medical procedures and protocols Excellent interpersonal and communication skills Ability to work effectively as part of a healthcare team Experience in a hospital setting, preferably in oncology Bachelor’s degree in Nuclear Medicine Technology or relevant field

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products, and Generics & APIs, comprising Solid Dosage Formulations & Active Pharmaceutical Ingredients. Jubilant Generics (JGL) is a wholly - owned subsidiary of Jubilant Pharma. JGL in India has Research & Development units at Noida and Mysore. It has two manufacturing facilities one at Mysore, Karnataka and another at Roorkee, Uttarakhand, engaged in APIs and Dosage manufacturing, respectively. The manufacturing location at Mysore is spread over 69 acres and it’s a USFDA approved site engaged in manufacturing of APIs, and caters to the sales worldwide. API portfolio focusses on Lifestyle driven Therapeutic Areas (CVS, CNS) and targets complex and newly approved molecules. The company is the market leader in four APIs and is amongst the top three players for another three APIs in its portfolio helping it maintain a high contribution margin. The manufacturing location at Roorkee, Uttarakhand is state of the art facility and is audited and approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA. This business focusses on B2B model for EU, Canada and emerging markets. Both manufacturing units are backward- integrated and are supported by around 500 research and development professionals based at Noida and Mysore. R&D works on Development of new products in API, Solid Dosage Formulations of Oral Solid, Sterile Injectable, Semi-Solids Ointments, Creams and Liquids. All BA/BE studies are done In house at our 80 Bed facility which is inspected and having approvals /certifications from The Drugs Controller General (India) and has global regulatory accreditations including USFDA, EMEA, ANVISA (Brazil), INFRAMED (Portugal Authority), NPRA(Malaysia), AGES MEA (Austria) for GCP and NABL, CAP accreditations for Path lab services. JGL’s full-fledged Regulatory Affairs & IPR professionals ensures unique portfolio of patents and product filings in regulatory and non-regulatory market. Revenue of Jubilant Pharma is constantly increasing and during the Financial Year 2018 -19 it was INR 53,240 Million as compared to INR 39,950 Million during the Financial Year 2017-18. Kindly refer www.jubilantpharma.com for more information about organization.

Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. Jubilant Pharmova Limited Jubilant Pharmova Limited (formerly Jubilant Life Sciences Limited) is a company with global presence that is involved in Radiopharma, Allergy Immunotherapy, CDMO Sterile Injectables, Contract Research Development and Manufacturing Organisation (CRDMO), Generics and Proprietary Novel Drugs businesses. In the Radiopharma business, the Company is involved in manufacturing and supply of Radiopharmaceuticals with a network of 46 radio-pharmacies in the US. The Company’s Allergy Immunotherapy business is involved in the manufacturing and supply of allergic extracts and venom products in the US and in some other markets such as Canada, Europe and Australia. Jubilant through its CDMO Sterile Injectables business offers manufacturing services including sterile fill and finish injectables (both liquid and lyophilization), full-service ophthalmic offer (liquids, ointments & creams) and ampoules. The CRDMO business of the Company includes the Drug Discovery Services business that provides contract research and development services through two world-class research centres in Bangalore and Noida in India and the CDMO-API business that is involved in the manufacturing of Active Pharmaceutical Ingredients. Jubilant Therapeutics is involved in Proprietary Novel Drugs business and is an innovative biopharmaceutical company developing breakthrough therapies in the area of oncology and autoimmune disorders. The company operates six manufacturing facilities that cater to all the regulated market including USA, Europe and other geographies. The Position Organization- Jubilant Pharmova Limited Designation - Digital Content Specialist. Location- Noida Job Summary: The role will be responsible for developing, curating, and managing high-quality content across various digital platforms to enhance brand visibility, engage target audiences, and support content and communication goals towards digital impression, SEO best practices, and content management systems, Collaborate closely with marketing, R&D and product teams to ensure content aligns with brand voice and business objectives . Key Responsibilities. Create, edit, proofread and publish engaging content for websites, blogs, email campaigns, and social media Work with internal teams and subject matter experts to generate thought leadership content. Ensure all content is aligned with brand voice, SEO best practices, and messaging guidelines. Enhance company presence on social, digital media through owned, earned, paid channels Track, analyze, and report performance metrics; optimize campaigns accordingly. Maintain consistent brand messaging throughout all platforms. Perform research on current benchmark trends and audience preferences Maintenance, audit and periodic refresh of 17 websites across the Jubilant Bhartia Group Governance and monitoring of 11 other group websites Working with BU teams to facilitate/ manage SEO, lead generation . Manage agency relationship and collaborate with IT, Business teams Supporting the development, execution, delivery and compliance of marketing collaterals in line with brand guidelines Nurturing the agency partner eco-system (Creative, production agencies) in line with procurement guidelines Budget management- Monitor expenses, track spends, report on budget Monthly, quarterly content calendar- execution and reviews on key communication pillars- Performance, Sustainability, People, Digital Transformation, CSR Plan, implement, and optimize paid campaigns on Google Ads, LinkedIn, Facebook, and other digital channels as & when required Monitor campaign KPIs including CTR, CPC, conversions, ROAS, and prepare performance reports. Person Profile . Qualification - Bachelor’s / Master’s degree in Mass Communication or related field. Experience – 8-10 years of relevant experience Content Creation and Brand Communications through various platform. Desired Certification & Must Have- Certification in Google Ads, digital marketing tools. Working knowledge of graphic tools (Canva, Adobe Suite) is a plus. Experience in B2B marketing is an advantage. Solid knowledge of SEO, keyword research and Google Analytics Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances.

Leading diagnostics center looking for a Nuclear Medicine Technologist in Chennai location. Qualification: B.Sc Nuclear Medicine Technology Experience: Fresher/Experience CTC: Up to INR 7.2L Per Annum Skills Required: - Good communication & interpersonal skills. - Detail-oriented & Analytical skills. - Should have good physical stamina. Roles & Responsibilities: - Preparing and administering radiopharmaceuticals orally or by injection or inhalation. - Explain test procedures and safety precautions to patients and provide them with assistance during procedures. - Operating imaging equipment, such as PET and SPECT scans. - Processing images on the brain, thyroid, bone, heart, lungs, kidneys, and liver on the computer. - Monitoring patients for unusual reactions to radioactive drugs. - Keeping detailed records of the amount and type of radiopharmaceutical used and of the procedure. - Ensure the environment is safe at all times for patient and staff. - Follow safety and disposal radiation procedures. - Maintaining and examining medical machines and imaging equipment. Only immediate joiners are required. Job Types: Full-time, Permanent, Fresher Pay: Up to ₹60,000.00 per month Benefits: Provident Fund Ability to commute/relocate: Purasawalkam, Chennai, Tamil Nadu: Reliably commute or planning to relocate before starting work (Preferred) Education: Bachelor's (Preferred) Experience: Nuclear Medicine Technologist: 1 year (Preferred) Work Location: In person

JOB DESCRIPTION Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Pharmova Limited Pharmova is born out of a combination of ‘ Pharma’ and ‘Nova’ (New) and Jubilant Pharmova Limited (formerly Jubilant Life Sciences Limited) will continue to focus on offering products and services with excellence in research and manufacturing, catering to the unmet health needs at an affordable price. It is an integrated global pharmaceuticals company having three business segments - Pharmaceuticals, Contract Research & Development Services and Proprietary Novel Drugs. Pharmaceuticals business through Jubilant Pharma Limited is engaged in manufacturing and supply of Radiopharmaceuticals with a network of 48 Radiopharmacies in the US, Allergy Therapy Products, Contract Manufacturing of Sterile Injectibles and Non-sterile products, Active Pharmaceutical Ingredients and Solid Dosage Formulations through six USFDA approved manufacturing facilities in the US, Canada and India. Contract Research & Development Services business represented by Jubilant Biosys Limited provides innovation and collaborative research to global pharmaceutical innovators through two world-class research centers in Bengaluru and Noida in India. Proprietary Novel Drugs business through Jubilant Therapeutics Inc. is an innovative patient-centric biopharmaceutical company developing breakthrough therapies in the area of oncology and autoimmune disorders. The Position Organization : - Jubilant Pharmova Limited Designation : - Manager, Indirect Taxation Location : - Noida Reporting Manager : - EVP & Head - Indirect Tax Key Responsibilities Ensure Indirect tax statutory compliances like timely filing of GST returns i.e.GSTR 1, 3B & ISD Effectively handling litigations, Drafting, show cause notice replies, preparation and submission of Appeals. Appearing before the authorities for personal hearing in Indirect Tax matters. Indirect Tax Advisory. Transaction Advisory and Vetting. Tax optimization, identification, and resolution of probable Indirect Tax issues. Timely advice on changes in Indirect Tax laws to business and Management and ensure its implementation. Guide the indirect tax personnel in the factory on the changes in the GST laws and ensure they are updated Perform & Coordinate Indirect tax audits, inspections, support in completion of old VAT assessments. Look out opportunities for digitizing, applying technology in the relevant indirect tax areas to improve compliance and enhance ERP system. Liaisioning with Government departments to ensure assessments/Litigations are closed successfully. Person Profile Qualification: - CA /ICWA /Bachelor of Law (National law college) Experience/ Industry:- Min. of 8-10 years of experience in Indirect tax with thorough knowledge of laws and procedures relating to GST/ Customs. Candidates earlier worked in manufacturing /service organisations preferably in Chemicals/Pharma industry are preferred. Candidates worked in Big4 or Consulting Companies are also suitable subject to having the relevant experience. Traits/Competencies Pro-active in approach, effective communication skills, Drive for results, Problem solving and right attitude. Willingness to work hard and focus on results. Strong orientation towards digitization, tech savvy and good MS office skills. Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances. To know more about us, please visit our website: www.jubilantpharmova.com

Leading diagnostics center looking for a Nuclear Medicine Technologist in Chennai location. Qualification: B.Sc Nuclear Medicine Technology Experience: Fresher/Experience CTC: Up to INR 7.2L Per Annum Skills Required: - Good communication & interpersonal skills. - Detail-oriented & Analytical skills. - Should have good physical stamina. Roles & Responsibilities: - Preparing and administering radiopharmaceuticals orally or by injection or inhalation. - Explain test procedures and safety precautions to patients and provide them with assistance during procedures. - Operating imaging equipment, such as PET and SPECT scans. - Processing images on the brain, thyroid, bone, heart, lungs, kidneys, and liver on the computer. - Monitoring patients for unusual reactions to radioactive drugs. - Keeping detailed records of the amount and type of radiopharmaceutical used and of the procedure. - Ensure the environment is safe at all times for patient and staff. - Follow safety and disposal radiation procedures. - Maintaining and examining medical machines and imaging equipment. Only immediate joiners are required. Job Types: Full-time, Permanent, Fresher Pay: Up to ₹60,000.00 per month Benefits: Provident Fund Ability to commute/relocate: Purasawalkam, Chennai, Tamil Nadu: Reliably commute or planning to relocate before starting work (Preferred) Education: Bachelor's (Preferred) Experience: Nuclear Medicine Technologist: 1 year (Preferred) Work Location: In person

You will be joining CANCER TREATMENT SERVICES HYDERABAD PRIVATE LIMITED, a hospital & health care company located in Nallagandla Village, Serilingampally Mandal, Hyderabad, Telangana, India. Our focus is on delivering top-quality cancer treatment and healthcare services. We are committed to providing exceptional medical care using cutting-edge technology while maintaining a compassionate approach towards patient care. As a Nuclear Medicine Technologist based in Sri Ganganagar, you will be expected to work full-time on-site. Your primary responsibilities will include preparing and administering radiopharmaceuticals, operating imaging equipment, ensuring patient safety, and adhering to radiation safety standards. Direct patient interaction is a key aspect of this role, involving the preparation of patients for procedures and the interpretation of diagnostic scans under the supervision of a physician. To excel in this role, you should possess the following qualifications: - Certification from the American Registry of Radiologic Technologists (ARRT) - Proficiency in Radiation Safety and compliance protocols - Experience in Nuclear Medicine and handling Radiopharmaceuticals - Strong knowledge of medical procedures and patient care practices - Excellent communication and interpersonal skills - Ability to work both independently and collaboratively within a healthcare team - Prior experience in a hospital or healthcare environment would be advantageous - A degree in Nuclear Medicine Technology or a related field If you meet these qualifications and are passionate about providing high-quality healthcare services, we welcome you to apply for this challenging and rewarding position at our esteemed organization.,

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products, and Generics & APIs, comprising Solid Dosage Formulations & Active Pharmaceutical Ingredients. Jubilant Generics (JGL) is a wholly - owned subsidiary of Jubilant Pharma. JGL in India has Research & Development units at Noida and Mysore. It has two manufacturing facilities one at Mysore, Karnataka and another at Roorkee, Uttarakhand, engaged in APIs and Dosage manufacturing, respectively. The manufacturing location at Mysore is spread over 69 acres and it’s a USFDA approved site engaged in manufacturing of APIs, and caters to the sales worldwide. API portfolio focusses on Lifestyle driven Therapeutic Areas (CVS, CNS) and targets complex and newly approved molecules. The company is the market leader in four APIs and is amongst the top three players for another three APIs in its portfolio helping it maintain a high contribution margin. The manufacturing location at Roorkee, Uttarakhand is state of the art facility and is audited and approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA. This business focusses on B2B model for EU, Canada and emerging markets. Both manufacturing units are backward- integrated and are supported by around 500 research and development professionals based at Noida and Mysore. R&D works on Development of new products in API, Solid Dosage Formulations of Oral Solid, Sterile Injectable, Semi-Solids Ointments, Creams and Liquids. All BA/BE studies are done In house at our 80 Bed facility which is inspected and having approvals /certifications from The Drugs Controller General (India) and has global regulatory accreditations including USFDA, EMEA, ANVISA (Brazil), INFRAMED (Portugal Authority), NPRA(Malaysia), AGES MEA (Austria) for GCP and NABL, CAP accreditations for Path lab services. JGL’s full-fledged Regulatory Affairs & IPR professionals ensures unique portfolio of patents and product filings in regulatory and non-regulatory market. Revenue of Jubilant Pharma is constantly increasing and during the Financial Year 2018 -19 it was INR 53,240 Million as compared to INR 39,950 Million during the Financial Year 2017-18. Kindly refer www.jubilantpharma.com for more information about organization. Scope of the role Scope - This role is responsible for Responsibilities – Achievement of set targets. Maintaining set call Average/coverage. Complete use of allotted resources. Increasing prescriber base Focus on target customers. Maintaining call average and customer coverage Increasing PCPM. Timely reporting. Ensuring ROI Relationships around the role Reporting to (Business) Regional Sales Manager / Sr. Regional Sales Manager Reporting to (Matrix) NA No of Reportees Direct NA Indirect NA Key External Stakeholder(s) Doctors, Stockiest, Retailers, CFA staff, Fellow professionals, institutional administrators Key Internal Stakeholder(s) RSM, ZSM, BDM, NSM / SM, PMT, HR & Sales Admin Competencies critical for the role Scientific/ Technical Competencies Proficiency level Convincing ability Presentation Selling Communication Behavioral Analytical ability PR Skills Qualifications Academic qualifications and experience required for the role Required Educational Qualification & Relevant experience Desirable - B.Pharm / D.Pharm / BSc. + MBA Essential - Graduates in any discipline Experience: 6 Months. to 2 years as a Medical Rep in a reputed organization. Age should be around 28 years

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products, and Generics & APIs, comprising Solid Dosage Formulations & Active Pharmaceutical Ingredients. Jubilant Generics (JGL) is a wholly - owned subsidiary of Jubilant Pharma. JGL in India has Research & Development units at Noida and Mysore. It has two manufacturing facilities one at Mysore, Karnataka and another at Roorkee, Uttarakhand, engaged in APIs and Dosage manufacturing, respectively. The manufacturing location at Mysore is spread over 69 acres and it’s a USFDA approved site engaged in manufacturing of APIs, and caters to the sales worldwide. API portfolio focusses on Lifestyle driven Therapeutic Areas (CVS, CNS) and targets complex and newly approved molecules. The company is the market leader in four APIs and is amongst the top three players for another three APIs in its portfolio helping it maintain a high contribution margin. The manufacturing location at Roorkee, Uttarakhand is state of the art facility and is audited and approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA. This business focusses on B2B model for EU, Canada and emerging markets. Both manufacturing units are backward- integrated and are supported by around 500 research and development professionals based at Noida and Mysore. R&D works on Development of new products in API, Solid Dosage Formulations of Oral Solid, Sterile Injectable, Semi-Solids Ointments, Creams and Liquids. All BA/BE studies are done In house at our 80 Bed facility which is inspected and having approvals /certifications from The Drugs Controller General (India) and has global regulatory accreditations including USFDA, EMEA, ANVISA (Brazil), INFRAMED (Portugal Authority), NPRA(Malaysia), AGES MEA (Austria) for GCP and NABL, CAP accreditations for Path lab services. JGL’s full-fledged Regulatory Affairs & IPR professionals ensures unique portfolio of patents and product filings in regulatory and non-regulatory market. Revenue of Jubilant Pharma is constantly increasing and during the Financial Year 2018 -19 it was INR 53,240 Million as compared to INR 39,950 Million during the Financial Year 2017-18. Kindly refer www.jubilantpharma.com for more information about organization. Scope of the role Scope - This role is responsible for Responsibilities – Supervision & Control Managing Team Brand growth Prescription Growth Prescribers growth Market Share Ensuring ROI Development of subordinates Relationships around the role Reporting to (Business) Zonal Sales Manager Reporting to (Matrix) NA No of Reportees Direct 4-5 Indirect NA Key External Stakeholder(s) Doctors, Stockiest, Retailers, CFA staff, Fellow professionals, Institutional administrators Key Internal Stakeholder(s) Superiors, Subordinates , PMT, HR & Sales Admin Competencies critical for the role Scientific/ Technical Competencies Proficiency level Proven Leadership qualities Good communicator Proven track records Ambitious Behavioral Analytical ability PR Skills Dependable Contributor Good Products knowledge Creative & Assertive Qualifications Academic qualifications and experience required for the role Required Educational Qualification & Relevant experience Desirable - B.Pharm / D.Pharm / BSc. + MBA Essential - Graduates in any discipline Experience : 5 to 7 years of Total experience and 1 – 2 years of First Line experience Age should be around 32 years

Radiographer Qualification – Diploma/ B.Sc in Radiology Job Responsibility Completing the guests' intake process, taking guests' histories, and preparing and educating guests about the imaging procedure. Preparing radiopharmaceuticals for contrast in the diagnostic images. Positioning guests and equipment to capture the correct area and produce clear images. Monitoring guests and ensuring their safety during imaging procedures. Calibrating the equipment to ensure clear, usable images are taken of the correct area, as specified by the Doctor. Logging and organizing image results, developing film, assisting with the interpretation of the radiograph results. Ensuring the proper sterilization and storage of the equipment, maintaining radiographic equipment, and reporting any equipment failures. Coordinating with the radiology department to schedule and complete radiographic procedures. Maintaining up to date knowledge of current radiology practices. Keralites candidates are preferred and ready to relocate to calicut. Job Type: Full-time Pay: Up to ₹20,000.00 per month Benefits: Food provided Health insurance Provident Fund Work Location: In person Application Deadline: 10/09/2025 Expected Start Date: 19/09/2025

As a Nuclear Medicine Specialist at Cancer Centers of America (CCA), you will play a crucial role in diagnosing and treating patients through innovative nuclear medicine procedures. Your responsibilities will include consulting with patients and healthcare providers to determine the most suitable nuclear medicine procedures, administering radiopharmaceuticals, interpreting scan results, evaluating patient medical histories, and prescribing treatments. You will also be responsible for monitoring patients during procedures, providing patient care, and ensuring radiation safety measures are adhered to. In this role, you will be at the forefront of advancements in nuclear medicine, conducting research to develop new techniques and procedures. Collaboration with other healthcare professionals, staying updated with industry standards, regulations, and advancements, and educating patients and their families about nuclear medicine procedures will be key aspects of your job. Additionally, you will be involved in ordering and maintaining necessary supplies and equipment for nuclear medicine procedures. To excel in this position, you should have expertise in Nuclear Medicine, experience in Cardiology and Emergency Medicine contexts, and proficiency in collaborating with physicians and medical teams. Strong analytical, problem-solving, and decision-making skills, excellent communication, and interpersonal abilities are essential. Advanced certifications in Nuclear Medicine, relevant board certifications, and a medical degree with specialization in Nuclear Medicine are preferred qualifications. Join CCA in its mission to provide world-class cancer care by applying your skills and knowledge in Nuclear Medicine to make a positive impact on the lives of those affected by cancer.,

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products, and Generics & APIs, comprising Solid Dosage Formulations & Active Pharmaceutical Ingredients. Jubilant Generics (JGL) is a wholly - owned subsidiary of Jubilant Pharma. JGL in India has Research & Development units at Noida and Mysore. It has two manufacturing facilities one at Mysore, Karnataka and another at Roorkee, Uttarakhand, engaged in APIs and Dosage manufacturing, respectively. The manufacturing location at Mysore is spread over 69 acres and it’s a USFDA approved site engaged in manufacturing of APIs, and caters to the sales worldwide. API portfolio focusses on Lifestyle driven Therapeutic Areas (CVS, CNS) and targets complex and newly approved molecules. The company is the market leader in four APIs and is amongst the top three players for another three APIs in its portfolio helping it maintain a high contribution margin. The manufacturing location at Roorkee, Uttarakhand is state of the art facility and is audited and approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA. This business focusses on B2B model for EU, Canada and emerging markets. Both manufacturing units are backward- integrated and are supported by around 500 research and development professionals based at Noida and Mysore. R&D works on Development of new products in API, Solid Dosage Formulations of Oral Solid, Sterile Injectable, Semi-Solids Ointments, Creams and Liquids. All BA/BE studies are done In house at our 80 Bed facility which is inspected and having approvals /certifications from The Drugs Controller General (India) and has global regulatory accreditations including USFDA, EMEA, ANVISA (Brazil), INFRAMED (Portugal Authority), NPRA(Malaysia), AGES MEA (Austria) for GCP and NABL, CAP accreditations for Path lab services. JGL’s full-fledged Regulatory Affairs & IPR professionals ensures unique portfolio of patents and product filings in regulatory and non-regulatory market. Revenue of Jubilant Pharma is constantly increasing and during the Financial Year 2018 -19 it was INR 53,240 Million as compared to INR 39,950 Million during the Financial Year 2017-18. Kindly refer www.jubilantpharma.com for more information about organization.

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products, and Generics & APIs, comprising Solid Dosage Formulations & Active Pharmaceutical Ingredients. Jubilant Generics (JGL) is a wholly - owned subsidiary of Jubilant Pharma. JGL in India has Research & Development units at Noida and Mysore. It has two manufacturing facilities one at Mysore, Karnataka and another at Roorkee, Uttarakhand, engaged in APIs and Dosage manufacturing, respectively. The manufacturing location at Mysore is spread over 69 acres and it’s a USFDA approved site engaged in manufacturing of APIs, and caters to the sales worldwide. API portfolio focusses on Lifestyle driven Therapeutic Areas (CVS, CNS) and targets complex and newly approved molecules. The company is the market leader in four APIs and is amongst the top three players for another three APIs in its portfolio helping it maintain a high contribution margin. The manufacturing location at Roorkee, Uttarakhand is state of the art facility and is audited and approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA. This business focusses on B2B model for EU, Canada and emerging markets. Both manufacturing units are backward- integrated and are supported by around 500 research and development professionals based at Noida and Mysore. R&D works on Development of new products in API, Solid Dosage Formulations of Oral Solid, Sterile Injectable, Semi-Solids Ointments, Creams and Liquids. All BA/BE studies are done In house at our 80 Bed facility which is inspected and having approvals /certifications from The Drugs Controller General (India) and has global regulatory accreditations including USFDA, EMEA, ANVISA (Brazil), INFRAMED (Portugal Authority), NPRA(Malaysia), AGES MEA (Austria) for GCP and NABL, CAP accreditations for Path lab services. JGL’s full-fledged Regulatory Affairs & IPR professionals ensures unique portfolio of patents and product filings in regulatory and non-regulatory market. Revenue of Jubilant Pharma is constantly increasing and during the Financial Year 2018 -19 it was INR 53,240 Million as compared to INR 39,950 Million during the Financial Year 2017-18. Kindly refer www.jubilantpharma.com for more information about organization. SOP Responsible for preparation of SOPs of IPQA Batch Manufacturing Documents Responsible for monitoring and ensuring on line review of batch manufacturing documents, batch packing documents Responsible for review of batch manufacturing Packaging and Analytical records, equipment logs etc. before batch release In process Controls Responsible for carrying out In Process control tests, line clearances activities, sampling during process validations, cleaning validation, batch manufacturing, packing GMP monitoring Responsible for monitoring adherence to various cGMP activities and laid down procedures in receipt, storage, testing, processing and dispatch of products