3773 Pharma Jobs - Page 46

Role: Group Product Manager Experience: 8 to 12 years of product marketing experience Qualification: B. Pharma + MBA - Marketing OR Pharma. Management Therapy/Department: CNS therapy (preferred), we are open to consider candidates from any therapy Industry Preference: Pharma only Job Location: Sun House, Mumbai Areas of responsibilities: Development of marketing and promotional plans for products to support the end consumers need Ensuring marketing strategy implementation through sales force connect Providing training, product knowledge, and direction to the field sales team to ensure that they are well-equipped with scientific and communication skills both. Developing brand plans/strategies for the product range along with market penetration strategy market research and competitor analysis. Creating brand inputs for promotion like VA, LBL, Newsletter, flipcharts, or digital campaigns like a website or app launch or webinar series, etc. Conducting meetings, scientific symposia, CMEs, and conferences, and ensuring brand visibility in the target audience segment of the pharmaceutical industry, which are healthcare professionals and hospitals. Motivating sales team members by organizing training camps, award ceremonies, and recognition programs. Product forecasting, new product pipeline strategy, new product pre-launch and launch strategy and post-launch, new initiatives for product growth strategy.

JOB DESCRIPTION Job Title: Technical Training Associate Job Location: Syngene International Limited, Biocon SEZ, Biocon Park, Plot No. 2, 3, 4 & 5, Bommasandra Industrial Area, Jigani Link Road, Bengaluru, Karnataka 560099, India (IND) About Syngene : Syngene ( www. syngeneintl. com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Core Purpose of the Role: Deliver training for GxP courses, including GMP, GDP, DI, and personal hygiene. Act as LMS administrator in SAP SuccessFactors for tasks like SCORM creation, exam unlocking, course assignments, ILT creation, assignment profile setup, addition of instructors, AICC content uploads, item ID creation, and other LMS-related activities. Update training modules and questions in the LMS. Conduct annual LMS upgrades based on SAP system updates. Coordinate with training coordinators and stakeholders across SYNGENE for training compliance Revise SOPs and provide training to departmental training coordinators. Maintain and update the training schedule, including monthly training and the annual training calendar. Manage GTR, attendance updates in LMS, and external training data entries. Develop and deliver training for VR modules. Monitor training files for client and regulatory audit compliance, ensuring necessary documentation. Collaborate on external training initiatives with organizations like USP India, PDA, and ISPE. Verify the effectiveness of SOPs in EDMS to align with world-class standards. Conduct monthly spot checks for department compliance as per the training SOP checklist. Compile MES data for QGF, QMR, risk registers, and quality town hall presentations. Prepare pending reports for the training department and summaries of overdue signoffs. Role Accountabilities: Accountable for the above-assigned role Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience: 3-6 Years Demonstrated Capability: as per the above role Education: Any master s degree, M. Pharma/ M. Sc. Will be preferred Experience: 3-6 years Skills and Capabilities: LMS, EDMS, Track-wise, articulate 360, Microsoft Office, self-motivated, able to communicate in English Education Any master s degree, M. Pharma/ M. Sc. Will be preferred Equal Opportunity Employer .

JOB DESCRIPTION Designation: Research Scientist (7-I) Job Location: Bangalore Department: DAS About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation . Job Purpose (1-2 Lines): Lead a team of scientists specializing in NMR spectroscopy. Key Responsibilities: (Maximum 5-8 Points) Structural elucidation of small molecules (organics) using state-of-the-art NMR methodologies Structure characterization of organic molecules. Collaborate closely with project teams. Solve complex technical problems with the equipment which could include software, hardware, or experimental set-ups. Maintains superconducting magnets, including scheduling cryogen deliveries; weekly liquid nitrogen fills and liquid helium fills. Proven hands-on experience in small-molecule NMR spectroscopy. Strong background in organic chemistry and structure elucidation Expertise in NMR methods with proficiency in NMR data systems and pulse sequence language. Strong written and communication skills. Ability to collaborate with project teams and work in a fast-paced team environment . Review of daily/monthly laboratory monitoring, verification, and calibration records of equipment and instruments. Understanding and demonstrating responsibility for the safety of self & colleagues by following all safety protocols provided by Syngene. Adherence to all environment, health, and safety (EHS) policies & standards are always in the workplace. Educational Qualification: MSc in analytical chemistry or allied disciplines. Technical/functional Skills: (Maximum 4-6 Points) NMR and LCMS. Experience: 10 to 15 years of hands-on experience on preparative HPLC Behavioral Skills: Must have very good communication skills Equal Opportunity Employer: .

Designation: Senior Executive Job Location: Bangalore Department: EAM About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation . Job Purpose We are seeking a skilled and proactive Electrical and Utility Executive to oversee the maintenance, operation, and optimization of electrical systems and utility services within our facility. The ideal candidate will ensure uninterrupted power supply, efficient utility management, and compliance with safety and regulatory standards This role focuses on the engineering and maintenance of formulation injectable and OSD facility systems, supporting the engineering team in optimizing performance and enhancing organizational competency while adhering to delivery, quality, and safety standards. Responsibilities include ensuring the timely resolution of equipment breakdowns, analyzing instrument failures, and reviewing of Utility system to ensure the seamless operation of Utility, HVAC and Electrical equipment s and systems. Key Responsibilities: Maintain electrical systems including HT/LT panels and UPS systems. Operation and maintenance of all utilities during shift and day -to-day operations. Monitor and manage utility services such as BMS, water supply, compressed air, HVAC, Nitrogen, Air compressor, chilled water, Hot water and steam systems during shift hours. Conduct preventive and breakdown maintenance of electrical and utility equipment. Coordinate with vendors and contractors for service and maintenance activities. Ensure compliance with statutory regulations and safety standards. Maintain documentation related to electrical inspections, energy audits, and utility consumption. Implement energy-saving initiatives and monitor energy efficiency. Respond promptly to electrical faults and utility disruptions. Support installation and commissioning of new equipment and systems. Adherence to Standard Operating procedures, Safety, cGMP, QMS & EHS Requirements. Planning and coordinating with service provider to carry out external HVAC and maintenance activity Responsible for performing the HVAC and compressed air validation, requalification activities as per the schedule. Responsible to prepare master list and planners as per the schedule. Educational Qualification: BE in Electrical and Electronics engineering (E&E) Technical/functional Skills: Trouble shooting of Utility, Electrical and HVAC equipment s. Hands-on experience with BMS, EMS and HT/LT switchgear, and other industrial control systems. Knowledge of Power distribution and load management Familiarity with relevant standards like IEC, IS. Strong knowledge of electrical systems, utility operations, and safety protocols. Ability to read and interpret electrical schematics and technical manuals. Experience: 3-6 years of experience in electrical and utility maintenance in a manufacturing or industrial setup . Behavioral Skills: Strong problem-solving and analytical abilities. Excellent communication and teamwork skills. Ability to manage multiple projects and meet deadlines. Equal Opportunity Employer: .

Designation: Executive Job Location: Bangalore Department: Engineering and Maintenance About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation. Job Purpose To oversee and manage the tracking, maintenance, and calibration of instrumentation and automation systems, ensuring optimal performance and reliability of plant equipment Key Responsibilities: Calibration Maintenance Participate in calibration maintenance programs for plant equipment, machinery, and related facilities to ensure precision and compliance with standards. Routine Maintenance Perform regular instrumentation maintenance activities on equipment to prevent malfunctions and downtime. Record Keeping Maintain detailed records of calibration reports, schedules, and maintenance activities to ensure traceability and compliance. Performance Testing Conduct performance tests on plant equipment using devices such as tachometers, pressure gauges, flowmeters, ammeters, and voltmeters. Troubleshooting & Repair Diagnose, troubleshoot, update, and repair malfunctioning plant equipment including air handling units (AHU), drive units. Safety Compliance Ensure strict adherence to safe work practices and procedures, including lockout/tagout protocols and confined space regulations. Operation of Equipment Operate various utility and laboratory equipment as necessary to support plant operations. Educational Qualification: BE in Electronics & Communications or BE Instrumentations Technical/Functional Skills: Instrumentation Calibration: Expertise in calibrating various instruments such as pressure gauges, flowmeters, temperature, tachometers, ammeters, and voltmeters. Troubleshooting & Repair: Skilled in diagnosing, repairing, and maintaining instrumentation and automation systems, including pneumatic, hydraulic, and electrical components. Process Control Systems: Familiarity with PLCs (Programmable Logic Controllers), DCS (Distributed Control Systems), and SCADA systems used in plant automation. Safety Standards: Knowledge of industrial safety standards and procedures including lockout/tagout, confined space entry, and hazardous area classification. Data Analysis & Reporting: Skilled in maintaining calibration records, generating reports, and analyzing instrument performance data for compliance and optimization. Installation & Commissioning: Experience in installing, testing, and commissioning new instrumentation and automation equipment. Automation Systems: Familiarity with automation components such as sensors, actuators, controllers, and pneumatic/hydraulic control systems. Experience: 3-6 years in the relevant environment Behavioral Skills: Attention to Detail: Meticulous in performing calibrations, inspections, and maintenance to ensure accuracy and compliance with standards. Problem-Solving: Strong analytical skills to diagnose issues quickly and develop effective solutions for complex instrumentation problems. Communication: Clear and concise in reporting technical findings and collaborating with cross-functional teams including maintenance, operations, and safety. Time Management: Ability to prioritize tasks efficiently, manage multiple maintenance schedules, and meet deadlines without compromising quality. Adaptability: Flexible to work in changing environments and handle unexpected equipment breakdowns with calm and resourcefulness. Teamwork: Cooperative and supportive working style, able to work well with technicians, engineers, and operators. Safety-Conscious: Proactively adheres to safety protocols and promotes a culture of safe work practices within the team. Continuous Learning: Willingness to stay updated with the latest instrumentation technologies, calibration techniques, and industry best practices. Accountability: Takes ownership of tasks and responsibilities, ensuring reliability and consistency in maintenance and calibration work. Initiative: Proactively identifies areas for improvement and suggests innovative solutions to enhance process efficiency and equipment performance. Equal Opportunity Employer: .

JOB DESCRIPTION Designation: Research Scientist (7-I) Job Location: Bangalore Department: DAS About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation . Job Purpose (1-2 Lines): Lead a team of scientists specializing in LCMS Key Responsibilities: (Maximum 5-8 Points) Proven ability to independently develop analytical methods for both reverse-phase (achiral) and polar organic (chiral) separations, with experience in scaling up methods to preparative scale. Hands-on experience with LC-MS and UPLC techniques is a strong advantage. Skilled in performing minor instrument troubleshooting, calibrations, and recovery analyses as required. Excellent written and verbal communication skills. Strong adherence to company health, safety, and compliance protocols. Flexibility to undertake additional responsibilities from the Line Manager in alignment with business needs. Educational Qualification: MSc in analytical chemistry or allied disciplines. Technical/functional Skills: (Maximum 4-6 Points) HPLC and LCMS. Experience: 10 to 15 years of hands-on experience on LCMS, UPLC and HPLC Behavioral Skills: Must have very good communication skills Equal Opportunity Employer: .

Designation: AQA Reviewer Job Location: Bangalore Department: Analytical Quality Assurance About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scienti fi c 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 scienti fi c problems, improve R&D productivity, speed up time to market and lower the cost of innovation . Key Responsibilities: Review of analytical raw data (through ELN / manual) generated by analyst, protocols/ reports pertaining to the section as per the standard operating procedure and speci fi cation. Ensuring, verifying, and reviewing the instrument usage log periodically and accordingly checking the labels as per SOP. Review of Outsourced analytical report. Review of logbooks with respect to all activity performed in the lab. Responsible for taking any other job allocated by Department Head / Department In charge. Review of technical data in analytical document viz. Calculations, Chromatograms, method parameters, integration, logbook entries, WS/RS and Column usage records, method parameters, reconciliation, vendor COA and other technical data in analytical document. Responsible to ensure review and release of raw material and packing material in LIMS/SAP. Responsible to ensure review and release of cleaning samples, inprocess samples, calibration reports and standard qualification reports. Reviewer shall ensure the documents physically for availability of all the pages of ODS and supporting documents. Review the documents for completeness, compliance to good documentation practices, test results against specification limits or acceptance criteria as mentioned in protocol and reconciliation of forms issued as applicable Review of all the tests as specified in the specification/Request for analysis /validation protocol/sampling protocol have been carried out Review of all supporting documents like chromatograms, balance print outs, Instrument printouts are enclosed in sequential manner to the parent report with signature as applicable Review of the test results in COA against specification along with other relevant sample information before approval. In case of any discrepancy, immediately notify to the reporting manager or his designee or Head or designee GMP Analytical Laboratory. Ensuring of conducting regular GMP rounds at Quality Control Laboratory. Involving in the Laboratory incident investigation, review, and approval. Educational Quali fi cation: M. Sc (Life science / Chemistry)/ M. Pharm Technical/functional Skills: Good exposure in Enterprise Applications like SAP, Learning Management Systems, Trackwise, and Analytical laboratory Applications like Chromatography and Non-chromatography data Management. Well versed in electronic data audit review. Good Knowledge on handling the application software. Establish good Interpersonal skills with cross-functional teams. Experience: 9 to 12 Years experience in life science industry. Behavioural Skills: Strong commitment towards work, and a high level of dedication, enthusiasm, motivation, and persuasive ability in a team. Good speaking-listening-writing skills, attention to details, proactive self-starter. Ability to work successfully in a dynamic, ambiguous environment. Ability to meet tight deadlines and prioritize workloads. Ability to develop new ideas and creative solutions. Should be able to work in team and flexible for working in shifts. Should be a focused employee. Equal Opportunity Employer: .

Role: Modular Carpenter Industry Type: Interior and Decor Functional Area: Research & Development Role Category: Pharmaceutical & Biotechnology (Note: This seems misaligned; consider updating if incorrect) Employment Type: Full Time, Permanent Key Responsibilities: Ability to read and interpret blueprints Assist supervisors with structural design, planning, layout, and installation Conduct repair work and installation of modular cabinets and other fixtures Assess the quality of woodwork and materials Operate tools, machines, and other carpentry equipment Ensure compliance with local building codes, health and safety regulations Deliver excellent customer service Perform physically demanding tasks: standing, climbing, lifting heavy objects Requirements: High School diploma Recognized apprenticeship or minimum of 2 years relevant experience Additional certifications (if required) Good communication skills Physically fit with strong hand-eye coordination Basic knowledge of mathematics Education: UG: Diploma in Mechanical PG: Not Required How to Apply: Send your resume to: [email protected] Visit: www.lifeasyinterior.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. 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 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 ",

The Opportunity: ArisGlobal is seeking a Associate Director - Product Management - Agentic AI to both create and grow a strategic revenue-generating product line within our Agentic AI solutions platform. In this role, you will translate high-priority opportunity areas into products, iterating quickly toward validated outcomes. You ll combine practical product leadership with commercial thinking, leveraging your understanding of emerging AI opportunities to inform our broader platform trajectory. This is a customer-facing, zero-to-one build role, ideally suited to someone with a background in data-driven decision support and insight generation, combined with experience of developing Agentic AI propositions. Key Responsibilities: Product Creation, Management & Growth: Drive the zero-to-one product build, leveraging entrepreneurial DNA and experience with lean startup, design thinking, service design, and other relevant methodologies. Translate strategic priorities into roadmaps, MVP definitions, user stories, and delivery plans. Operate with autonomy and pace, taking new products from concept through early validation to scale. Identify opportunities to increase revenue, lower operational costs, and improve customer retention by analyzing product performance and customer feedback. Customer Development: Engage with key stakeholders in life sciences to validate need, value, and usability. Run lean product discovery cycles across hypothesis-driven themes. Serve as a key external representative of the product trusted, credible, and customer-aware. Cross-Functional Collaboration: Work collaboratively across internal teams including Engineering, Sales, Services, and Marketing to ensure alignment on product priorities, effective go-to-market execution, and customer adoption. Work, as needed, with key external partnerships, as required to build out and commercialise new propositions. Clearly communicate product vision and benefits to internal stakeholders, enabling effective product launches and adoption strategies. Why Join Us?: You ll help build one of the most strategic products within a bold new wave of Agentic AI capabilities. This is a rare chance to take full product ownership, drive innovation with real customer impact, and work within a supportive team that s moving fast to shape the future of AI-powered development in life sciences. Skill Requirements: Required: 12+ years of experience in Product Management in B2B2C, B2B, or B2C space. 3+ years in AI-focused product management in B2B2C, B2B, or B2C space. Good experience in Agentic AI Experience working closely and driving product requirements for Data Engineering, ML Engineering, and Data Science teams. Proven track record of launching AI-driven enterprise SaaS solutions at scale. Deep curiosity and awareness of emerging AI technologies and trends, along with an ability to conceptualize how they can drive practical business value. Analytical mindset, skilled at using metrics to drive product decisions and continuously improve user experience. Strong communication skills, comfortable translating complex ideas into clear business value for diverse stakeholders. Proven ability to prioritize and execute effectively in dynamic environments. Entrepreneurial DNA, with experience in zero-to-one product builds and methodologies such as lean startup, design thinking, and service design. Preferred: Prior experience building AI products or platforms designed to automate or augment enterprise workflows. Understanding of modern platform architectures, scalability, and performance considerations for AI-driven products. Formal degree in a technical field such as Machine Learning, Statistics, or Computer Science. Familiarity with core AI platform elements and knowledge of AI tooling stack across one/many public cloud and data vendors. Experience managing large, technically complex product programs spanning multiple teams. A high degree of independent drive. Experience in contextual intelligence, information design, and insight generation.

Roles and Responsibilities Responsible for planning stability studies, writing and/or review of stability protocols, reports and preparation of technical documents in CTD format. Co-ordinate and follow up stability studies at contract research organizations (CROs)/ Chemical Quality Control lab of Orion (CQC). Co-ordinate and follow up validation and method transfer at CROs. Write/check/review analytical and pharmaceutical documents as per regulatory requirements (method and validation documents/ variations/ additional question responses) Evaluate/ review method validation protocols / reports / analytical methods prepared by CROs. Reviewing and commenting on change controls, deviations, temperature excursions, stability data, process validation documents and troubleshooting etc. for externally supplied products. Write documents into Orion s IT systems for example analytical methods Writing of Product Quality Review (PQRs) for own production products and ensure its timely approval. Preparation and review of other documents related to PQRs. Requesting, follow-up and tracking of PQR related data. Review of Externally supplied PQRs, related coordination and follow up with vendor and and other stakeholders Theoretical evaluation of physico-chemical properties of the drug products and/or raw materials Co-operation with other departments/ partners Local in-licensing support To assist the overall working of Indian Pharmaceutical team Other possible tasks appointed by Supervisors Note: We do not have own laboratories in India! Primary Skills (essential) Minimum 4 years work experience in Analytical Development or Pharmaceutical product development or Quality Assurance activities in global Pharma industry Knowledge of EU and US requirements and ICH guidelines Practical development skills from the laboratory work and troubleshooting Task oriented with learning attitude and Teamwork skills Fluency in oral and written English Confirmed skills of Microsoft Office is essential Pharmaceutical education & practical analytical development skills also from the laboratory to production scale of different types of formulations (tablets, capsules, liquids, etc.) will have added advantage Candidate interested/experienced in above documentation work will be preferred. This job offers: An excellent opportunity to work in an inspiring and important role in the area of Pharmaceuticals Great opportunity to become part of the wholly owned subsidiary of globally operating Orion Group Possibility to utilize your own strengths with the support of the professionals Flexible, high spirit working environment where your skills are appreciated Good work-life balance Clear, transparent processes and responsible supervisors are our benefits to the personnel Education Masters degree in chemistry from a reputed College / University. At Orion, your work creates true impact and well-being for our customers, patients and society at large. Our culture of friendliness, respect, mutual appreciation and diversity creates a safe working environment where you can strive for excellence. We offer a wealth of career paths and development opportunities that support the development of innovative solutions and improving the quality of life. Please visit our website to find further information about our values and Orion as an employer https: / / www.orion.fi / en / careers / orion-as-an-employer / . How to apply and additional information Please fill Candidate Information Form on https: / / forms.gle / o9BhfmhigBcyp5fy7 & email your CV to recruitmentindia@orion.fi Required documents: CV/Resume Application deadline: 18.07.2025

CARE CHANGES EVERYTHING. Medical Product Manager Job Details Contract Type: Unlimited / Full-Time Country / City: India / Mumbai Company: NIVEA India Pvt. Ltd. Job Function: Marketing / Market Research Your Tasks As a Medical Product Manager at Beiersdorf, your primary responsibilities will encompass a range of critical tasks designed to enhance our position in the dermo-cosmetic sector. 1. Medical Detailing Execution You will be in charge of developing, adapting, and distributing medical marketing collaterals such as detailing aids, brand story decks, sampling kits, and clinical studies, ensuring that the right information reaches the market effectively. You will collaborate closely with the field force to guarantee a timely rollout of campaigns, ensuring that all materials are utilized effectively to meet our marketing objectives. 2. NPI & Campaign Management Leading the launch of new products at dermatology clinics, you will create and oversee best-in-class launch materials to captivate our audience. Your expertise will drive the execution of monthly in-clinic campaigns and visibility plans, coordinating across various teams to ensure full and timely deployment. 3. Medical Event Execution You will execute workshops, KOL meetings, and training events, collaborating effectively with field force and external partners to enhance our brand presence. 4. Digital Coordination (Medical) Your role will involve supporting digital content rollout including initiatives like WhatsApp campaigns and closed-loop medical mailers, which are essential in today s marketing landscape. You will ensure that all messaging aligns with approved claims and our established product dossier. 5. Analytics & Reporting Tracking campaign execution will be one of your key responsibilities, utilizing CRM and IQMed reports to gauge doctor engagement metrics and sample utilization. You will leverage IQVIA analytics to extract insights that inform our medical strategy and drive enhancements based on market feedback. 6. Cross-functional Support Coordination with regulatory, legal, and supply chain teams will be vital to align timelines and maintain compliance across all initiatives. You will also assist in developing internal Standard Operating Procedures (SOPs) to ensure a cohesive and compliant approach to medical marketing. Your Profile Work Experience: A solid background of 3-8 years in Rx product or brand management, with experience specifically in Derma/Cosmetic Derma therapy, is crucial. Educational Qualification: A Bachelor s degree in Pharmacy or a related field along with an MBA specializing in Pharma is required to equip you with the necessary industry knowledge and business acumen. Interpersonal Skills: Strong communications abilities will be essential for effective collaboration within teams and interactions with healthcare professionals. Adaptability and Problem-Solving: A proactive approach to identifying challenges and implementing solutions will be vital, as the market dynamics in the medical field can change rapidly. Additional information For further information please reach to your responsible recruiter Kartik Kulshrestha. Please apply online via the Beiersdorf Intranet until 21st July25. About Beiersdorf At Beiersdorf, we want to help people feel good about their skin and our commitment goes far beyond caring for skin. For 140 years, we have developed innovative skin and body care products for well-known brands such as NIVEA, Eucerin, La Prairie, Hansaplast, and Labello. We act according to our purpose, WE CARE BEYOND SKIN, and take responsibility for our consumers, our employees, the environment and society. Behind every brand, every product and every accomplishment are our more than 20,000 employees. It is for them that we live an inclusive culture of respect and trust that is strongly aligned with our values CARE, COURAGE, SIMPLICITY and TRUST. We also embrace diversity by valuing the uniqueness of each individual and being committed to equal opportunities for all. Further information can be found within our . YOUR BENEFITS Buddy and Mentoring International Work Environment Flexible Working Hours Attractive Salary Get to know: Maureen Marketing is more than selling its about shaping emotions, understanding people, and building connections. Its a journey of creativity, collaboration, and curiosity, where every campaign helps people fall in love with our brands and their skin. Through marketing, Ive learned to embrace challenges, stay curious, and unlock endless potential.

Officer - 3P Operations Job Details | Tata Consumer Products Limited Search by Keyword Search by Location Select how often (in days) to receive an alert: Select how often (in days) to receive an alert: Officer - 3P Operations Tata Consumer Products Limited Officer - External Manufacturing Tata Consumer Products Ltd. About the Job: Officer- External Manufacturing, Soulfull Product Supply Organization Manager External Manufacturing At Tata Consumer Products Ltd, we stand #Forbetter Planet, Sourcing, Nutrition, Communities. And #ForBetter Opportunities . Here s an exciting one! How does this Job align to our Strategy? At the core of Tata Consumer Products business approach lie six strategic pillars that serve as the foundation for its growth and success: Strengthening & Accelerating our Core Business, Digital and Innovation, a Future-Ready Organization, New Opportunities and Sustainability. This job opportunity closely aligns with one of these key strategic pillars, which is driving Strengthening & Accelerating our Core Business. The incumbent shall be responsible for managing multiple external foods manufacturing units. The job aims to bring tangible business value by strengthening & accelerating our core business. Where do you come in as? Director-External Manufacturing Senior Manager-External Manufacturing Officer External Manufacturing This job is at N-6 Level (N corresponds to CEO s level) Direct reports: NA Complexity of the role (Optional): NA Type of Role: Individual Contributor Primary Stakeholders (Optional) What are the Key Deliverables in this role? Financial Outcomes Monitor expenses, suggest cost effective alternatives and daily administrative operations. Implement robust processes, Controls on RM and FG, alignment basis planning functions, reconciliation of reports/data etc., develop scope of improvement for respective external foods manufacturing units and ensure exchange of information with proper coordination with all internal stakeholders (Finance, Logistic, Quality, Plant Team). Customer Service Timely production in the respective external foods manufacturing units as per planning. Monitoring timely compliance of regulatory audits, stock audits, Quality audits and understanding on root cause analysis and closures in plant/production/market levels. Understanding on product Quality is important. Coordination with cross functional departments to support/meet schedules. Effective delegation and supervision of all tasks in stipulated time. Internal Processes Demonstrate and troubleshoot production issues by analyzing data, investigating issues, identifying solutions, and recommending actions. Equipped in analytical thinking and problem-solving skills. Managing work as per approved DoA s, SOP s and SLA standards and tracking of month closing activities. Responsible for SAP related activities and its checks at all PC s. MIS management & planning further manufacturing activities accordingly. (Keep track of Demand & supply closely with help of SCM) Ensure that the respective external foods manufacturing units complies with the terms and conditions of the Quality standards to achieve adherence to specified quality levels. Ensure inventory and account reconciliation of vendors in alignment with commercial team. Timely & smooth execution of the NPD projects while coordinating with the internal and external stakeholders. Innovation and Learning Review Safety, Health, Hygiene, and other Food Safety compliances for the handled units & develop standardized Infrastructure and Processes for the respective external foods manufacturing units. Ensure closure all non compliances observed during audits within the stipulated time frame for the respective external manufacturing units (HACCP and Food safety audits). Training of Work force and driving company initiatives at the external foods manufacturing units What are the Critical success factors for the Role? Graduation (Food Tech./Diploma Engineering) having working experience in FMCG. Proficiency in SAP. Willingness to travel. What are the Desirable success factors for the Role? Minimum 3+ years of experience in FMCG/Pharma SC management and expertise in managing manufacturing operations. TCPL Growth Mindset and Behaviors We are obsessed about keeping Consumers & Customers first in our hearts that s why we are here ! We are trailblazers in executing with Excellence Together as One Team ! We take Ownership of our business delivering value for our Stakeholders .. no Compromises ! We are Open to Continuously improving Continuously innovating For Better ! We live & breathe our Tata Code of Conduct About Us: At Tata Consumer, we stand For Better. Tata Consumer Products is a focused consumer products company uniting the principal food and beverage interests of the Tata Group under one umbrella. Our brands embody our purpose of For Better through the value they deliver to consumers with a focus on innovation, health and wellness, convenience and premiumisation. The Company s portfolio of products includes tea, coffee, water, RTD, salt, pulses, spices, ready-to-cook and ready-to-eat offerings, breakfast cereals, snacks and mini meals. Our key brands include Tata Tea, Tetley, Eight O Clock Coffee, Tata Coffee Grand, Himalayan Natural Mineral Water, Tata Copper+ and Tata Gluco+, Tata Salt, Tata Sampann and Tata Soulfull. In India, Tata Consumer Products has a reach of over 200 million households, giving it an unparalleled ability to leverage the Tata brand in consumer products.

Title: Associate Manager - Marketing Operations Date: 8 Jul 2025 Location: Bangalore, KA, IN Job Description We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future-ready. We offer accelerated, global growth opportunities for talent that is bold, industrious and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship and is guided by passion, innovation, collaboration and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out www.careers.indegene.com What if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it We understand that you are looking for growth and variety in your career at this point and we would love you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career with the reliability you seek. We hire the best and trust them from day 1 to deliver global impact, handle teams and be responsible for the outcomes while our leaders support and mentor you. We are a profitable rapidly growing global organization and are scouting for the best talent for this phase of growth. With us, you are at the intersection of two of the most exciting industries of healthcare and technology. We offer global opportunities with fast-track careers while working with a team that is fueled by purpose. The combination of these will lead to a truly differentiated experience for you. If this excites you, then apply below. Role : Associate Manager - Marketing Operations Description: We are looking for an experienced and passionate digital marketer to lead and support the implementation and execution of omnichannel campaigns for key respiratory brands in selected EU countries. This role is a key member of an agile Scrum Team, supporting assigned brands to successfully deliver the team s mission. Key Responsibilities In this role, you will: Support the strategy and lead the execution of integrated omnichannel campaigns for assigned brands, ensuring timely delivery, customer segmentation, and precise targeting. Collaborate closely with Medical Affairs Managers to plan and execute campaigns, including digital customer experience (DCX) user journeys and multi-channel content planning. Coordinate with cross-functional stakeholders and external partners, such as media agencies and local operating company (LOC) representatives, to ensure seamless campaign delivery. Execute (or guide vendor execution) of content tagging and campaign performance tracking in alignment with the Client s analytics framework. Provide tagging instructions for all campaign assets. Conduct monthly performance reviews, analyze key data sets, extract insights, and present optimization recommendations to senior management during agile sprint retrospectives. Partner with digital and analytics leads to ensure optimal usage of global platforms, adopting the latest features, best practices, and tools. Manage forecasting and prioritization of content and campaign activities with vendors, ensuring governance and timely execution. Oversee digital and translation vendors, perform compliance checks and ongoing monitoring to mitigate risk. Lead the development, implementation, and continual refinement of a customer-centric digital marketing framework. What This Role Offers You This opportunity will allow you to grow your career by taking ownership of key digital marketing activities. You ll develop valuable experience in: Mindset: Adopting an agile and entrepreneurial mindset to innovate and solve complex marketing challenges. Must Have Capability: Proven success in omnichannel strategy and campaign execution, including media and content planning. Experience with third-party HCP marketing platforms and modular content strategies. Strong project planning and execution discipline. Ability to distill insights from analytics to optimize campaign effectiveness. Stakeholder Management: Effective collaboration with production agencies, Medical Affairs Managers, and external vendors. Coordinating with internal compliance, medical, and other subject matter experts. Customer Focus: Deep understanding of customer needs and digital industry trends to inform campaign design and delivery. Required Qualifications We are seeking professionals with the following qualifications: Experience working on Rx pharmaceutical brands. Degree in Digital Marketing or a related discipline, with strong experience in omnichannel execution. Understanding of customer segmentation and targeting strategies. Hands-on experience with content creation and copy approval processes (e.g., digital content platforms). Proven internal engagement skills and ability to build strong networks. High personal accountability and demonstrated success in delivering complex, high-impact projects. Good to have The following are not mandatory but would be a plus: Knowledge of the Asthma and COPD competitive landscape in one or more EU markets. Demonstrated excellence in building internal credibility and insight-sharing through a robust network. EQUAL OPPORTUNITY

Manager, Salesforce Marketing Cloud Engineer The Opportunity Based in Hyderabad - INDIA, join a global healthcare biopharma company and be part of a 130- year legacy of success backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare. Be part of an organisation driven by digital technology and data-backed approaches that support a diversified portfolio of prescription medicines, vaccines, and animal health products. Drive innovation and execution excellence. Be a part of a team with passion for using data, analytics, and insights to drive decision-making, and which creates custom software, allowing us to tackle some of the worlds greatest health threats. Our Technology Centres focus on creating a space where teams can come together to deliver business solutions that save and improve lives. An integral part of our company s IT operating model, Tech Centres are globally distributed locations where each IT division has employees to enable our digital transformation journey and drive business outcomes. These locations, in addition to the other sites, are essential to supporting our business and strategy. A focused group of leaders in each Tech Center helps to ensure we can manage and improve each location, from investing in growth, success, and well-being of our people, to making sure colleagues from each IT division feel a sense of belonging to managing critical emergencies. And together, we must leverage the strength of our team to collaborate globally to optimize connections and share best practices across the Tech Centres. Role Overview As a Salesforce Marketing Cloud and Customer Data Platform (CDP / aka Salesforce Data cloud ) Developer is responsible for designing, implementing, and managing marketing automation solutions using Salesforce Marketing Cloud and integrating customer data from various sources into a unified platform. This role combines technical skills with marketing knowledge to enhance customer engagement and optimize marketing strategies. You need to collaborate with team members to troubleshoot issues and ensure smooth project execution. This position is ideal for those looking to grow their skills in Salesforce eco-system. What will you do in this role Setup and Configuration : Configure Salesforce Marketing Cloud to align with business objectives, including setting up user roles, permissions, and security settings. Campaign Management : Understand, execute, and manage multi-channel marketing campaigns (email, SMS, social media) using Marketing Cloud tools. Data Integration : Integrate customer data from various sources (CRM systems, web analytics, third-party applications) into the Salesforce Data cloud Platform and ensure data accuracy, consistency, and integrity across all integrated systems. Segmentation Strategies : Develop and implement audience segmentation strategies based and Utilize customer data to create personalized marketing messages and experiences. Automation Creation : Build automated marketing workflows using Journey Builder and Automation Studio to enhance customer engagement and monitor and optimize automated processes for performance and efficiency. Performance Tracking : Create reports and dashboards to track the performance of marketing campaigns and customer engagement metrics and analyze campaign data to derive insights and make data-driven recommendations for future marketing strategies. Cross-Functional Collaboration : Work closely with developers/product managers and BA and other IT teams to understand requirements and deliver effective solutions and provide training and ongoing support to marketing teams on using Salesforce Marketing Cloud and CDP functionalities. What should you have: Bachelor s degree in computer science / information systems or equivalent technical field from a recognized University or Institute. 5+ years of relevant experience in developing and implementing complex solutions in Salesforce Platform at large scale project delivery model. 2+ years of hands-on experience with the Salesforce platform, preferably with a focus on Salesforce Marketing Cloud and Data Cloud (CDP) and proven track record of successful salesforce implementation, integration over API, configurations & Customization. In-depth knowledge of Salesforce Marketing Cloud components, including Email Studio, Journey Builder, Automation Studio, and Audience Builder. Should proficient enough in salesforce security, Sharing rule, Permission set, Trigger, OWD and profiles. Experience with AMP script, SQL, and other scripting languages for data manipulation and dynamic content creation. Good understanding of Data cloud concepts, overview on relational data modeling ( DMO and DLO), and customer segmentation strategies is needed. Nice to have some experience in integrating of multiple data sources into a Data cloud platform and managing customer profiles. Exposure in any script (Type Script, Java Script, Angular, Node etc ) and exposure in using APIs and ETL tools (e.g., MuleSoft, Informatica) and understanding of AWS services or serverless architecture is nice to have. Pharma domain experience is an added advantage. Strong analytical and problem-solving abilities with effective solutions are highly valued. Good verbal and written communication skills for effective collaboration with team members and stakeholders Should have a proper attitude to learn and adopt new technologies. Ability to stay updated with the latest Salesforce features and best practices. Salesforce Platform certification is preferable. Who we are What we look for #HYD IT2025 Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Employee Status: Regular Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Hybrid Shift: Valid Driving License: Hazardous Material(s): Required Skills: Business, Data Engineering, Data Visualization, Design Applications, Engineering Management, Human Resource Management, Leadership Management, Management Process, Manufacturing Engineering, Marketing, Marketing Management, Marketing Resource Management (MRM), Promotions Management, SAP HCM, Social Collaboration, Software Configurations, Software Development, Software Development Life Cycle (SDLC), Solution Architecture, System Designs, Systems Integration, Testing Preferred Skills: Job Posting End Date: 09/30/2025 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Establishing new business links Prospecting leads and contacting them to pitch the product Recruiting by selling career opportunity to prospective advisors Working towards achieving the sales target Collaborate within teams to achieve better results Required Candidate profile Any Graduate Mini. 1 Years of Exp. in Sales & Marketing Strong Communications Skills Local candidates are prefer For More Information - Contact : Meenaakshi P.| 9313653024

We’re hiring a full-time On-Field Sales Manager in Gujarat. Take charge of business, managing sales pipelines, build strong customer relationships, achieving monthly targets, handling deal closures, generating leads for the assigned location. Required Candidate profile “Candidates must hold a bachelor’s degree and have 2–5 years of experience in field sales and BFSI Sales also.” Bring your resume at +91 9327916832 – see you there!

This role supports the needs of the Global Analytics & Insights team, part of the Corporate Strategy Team, with a focus on providing Advanced Analytics (to include statistical modeling, regression analyses, market basket, churn modelling methods) to work on program/promotion design and ROI post program. Additional project-based work around price elasticity, mixed market modelling, segmentation, game theory modelling and predictive analytics (e. g. , customer lifetime value) will be in scope. The overarching goal of all work will be to find efficiencies in current promotional spend and optimize future business activities. This position is responsible for managing all aspects of project-based analyses including data preparation, analysis design, implementation using appropriate methods & results presentation. Leading readouts and review with internal customers. Lead discussions with customers to uncover needs, design and deliver analytics solutions. Enable measurement and improved effectiveness of rebates, media spend, pricing and sales force activities leveraging statistics and data science techniques. Collaborate with internal stakeholders, descriptive analytics team and cross-functional teams to solve business problems, propose efficiencies and innovative approaches. Constantly innovate in data science domain, constantly bringing new expertise to the team and adding to team knowledge Guide the junior members on technical and functional aspects, problem formulation, approach design, model building, model refinement and selection, reviewing and storyboarding the results. Consistent, constant alignment with all members of team in Greenfield, Indiana. Maintain an environment open to change and innovation, recognizing improvements in existing tools and anticipating new technologies to deliver world class analytics and maximize effectiveness Minimum Qualification (education, experience and/or training, required certifications): Bachelor s Degree in quantitative or management field. (Master s preferred) 6+ years of experience in Advanced Analytics, Commercial Effectiveness. Expertise in statistical modelling techniques - A/B testing, regression, clustering, classification, decision trees, forecasting. Expertise of probability models, market basket, churn modelling, segmentation and customer analytics. Advanced skills in Python, R and advanced excel. Proven analytical/problem solving skills with strong learning agility. Excellent written and verbal communication Demonstrated excellence in Power Point and storyboarding. Additional Skills Experience with Tableau, SQL. Experience with Azure ML & Model Deployment Experience with GitHub Project management experience across multiple business functions Experience in pharma/retail domain Additional Information: Travel Percentage: 0-10%

ESG Data Reporting & Governance Help in building a long-term plan in line with global strategy on sustainability mandate Knowledge and ability to drive all ESG related actions and reporting requirement for BRSR, CDP, S&P Global (DJSI), UNGC, Annual Sustainability Reporting, MSCI, Sustainanalytics, etc. Knowledge and understanding on ESG Reporting Standards - GRI, UNSDG, SBTI, NGRBC Principles for BRSR Reporting Guide internal teams/departments to improve their ESG framework and reporting Data/information collation for all reporting requirements. Follow-up with various departments/teams across locations and functions to collect data and information. Expertise in analysing the data collated and ability to discuss with concerned stakeholders for any data issues, probable gaps and corrections. Gap assessment and recommending ESG improvements to the senior management. Lead all reporting compilation including liaison with external partners towards timely closure Leading assurance (audit) for ESG related disclosures Prepare quarterly ESG updates for presenting to the Board, Managing Director and Senior Management. Suggest improvement areas and action plan for such improvements. Preferred Education Qualifications and Experience B. E. , Chemical/Mechanical engineering from an accredited university/college with minimum of 8 to 10 years experience in ESG domain. M-Tech/MBA in Sustainability Understanding of ESG Standards/Reporting Framework, practices and challenges. Strong verbal, written communication, analytical skills and ability to engage stakeholders across functions and grades; Work well in teams Ability to manage multiple priorities and a variable workload and flexible to handle peak load Willingness to take up overall ownership and not limited by letter of job description for role and responsibility Demonstrated proficiency in multiple business applications: MS office, especially power point, Excel, MS-Word, etc.

We need different Profile candidates for so many designations in TRICITY, Ambala and nearby areas. So, please apply as soon as possible so that you can grab the opportunities. Male and Female both may apply Required Candidate profile Some of the job profiles are as follows for the reference HR BDM VISA Counselor IELTS, PTE CRM Telecallers Front office Office Manager Admin Marketing Technical IT Jobs Teachers And more

" Job Title: Head Procurement - Raw Materials (DGM/ GM) Location: Mumbai Reporting to: Commercial Head About the client: PSS has been mandated to hire the Head of Procurement - Raw Materials for a well-established and highly reputed Indian pharma company manufacturing formulations OSD and Injectables. Key Responsibilities: Department: Procurement Raw Materials Location: Mumbai HO Reporting to: Commercial Head Job Responsibilities: Overseeing the sourcing and procurement of Raw Materials for the manufacturing plants. Identifying, evaluating, and developing new vendors by inviting quotations, negotiating, and pricing. Preparing comparison statements, obtaining the necessary approvals, and processing the orders. Obtaining all supportive regulatory documents for filing drug dossiers. Follow up with vendors for dispatch details. Follow up with the Logistics team / CHA for clearance of the material. Preparing the raw material cost estimations for projects based on the requirement. You will be responsible for Vendor development, Vendor Audit, and Ongoing Vendor Management, meeting Quality, Food Safety, and other regulatory requirements of the industry. You will ensure procurement of Quality & quantity on time with a focus on Cost optimization and savings. Educational Qualifications and Experience: MBA in Operations/ Supply Chain with 15 years of work experience in the Procurement of Raw Materials in the Pharma industry. Good understanding of procurement processes in a manufacturing setup, commercial acumen, ability to negotiate, supply chain. Ability to manage internal and external stakeholders of the company. #LI-NV1 ",

Job Summary Investigations will support in conducting forensic investigations and fraud risk assessments across Sun Pharma s global operations. The role requires strong analytical skills, discretion, and the ability to manage sensitive matters independently and professionally. Areas of Responsibility Assist in end-to-end forensic investigations globally Conduct fraud data analytics and background checks using tools like Intella Pro and Falcon NEO2 Analyse digital evidence, databases, and systems to identify anomalies Conduct interviews with suspects and witnesses with professionalism Prepare investigation reports and summaries for internal stakeholders Collaborate with Legal and HR on disciplinary and legal actions Support co-sourced engagements and manage external consultants Contribute to the continuous improvement of investigative methodologies and internal control Key Skills: Strong verbal and written communication Stakeholder engagement and relationship management Analytical mindset with investigative acumen Ability to work under pressure and manage sensitive situations Project management and attention to detail Ethical conduct and discretion

About the job: Position: Robotic Process Automation Service Owner Department: Business Operations Reports to: Digital Delivery and Operations - Transversal Programs - Automation CoE Manager What you will be doing: The RPA Service Owner is responsible and accountable for the comprehensive management of the RPA service, encompassing its design, cost-effectiveness, quality assurance, and user satisfaction. This role serves as the primary liaison with outsourced support management groups, ensuring Sanofis priorities are addressed and internal policies are implemented through regular audits and quality checks. The RPA Service Owner is the key point of contact for business escalations. Main Responsibilities: Service Design and Improvement Lead and own the RPA services (run and evolution) Design and implement continuous improvements in order to optimize processes and services under his/her responsibility Develop and monitor relevant KPIs to assess service quality Cost Management Oversee all financial aspects of the RPA service (run budget management) Optimize resource allocation for maximum efficiency Quality Assurance Drive improvements in service quality and user satisfaction Conduct regular service performance reviews Compliance and Contract Management Ensure adherence to Service Level Agreements (SLAs), Operational Level Agreements (OLAs), and other contracts Manage license contract approvals, purchase orders, and good receipts Regularly review incident backlogs, prioritizing based on urgency, volume, and age Develop and monitor remediation plans for quality issues Oversee change management processes and templates Business Representation and Stakeholder Management Act as the primary owner and representative of the RPA service to the business Ensure accuracy, quality, and SLA compliance in daily operations Implement and monitor KPIs for tracking incidents and request queues Liaise with support group leaders to ensure provider commitments are met Manage relationship with digital stakeholders (digital tech, risk and quality, architecture, ) in the frame of the RPA service. Experience / Knowledge 5+ years of experience in IT Service Management or RPA support roles Proven experience leading support teams and managing service delivery (transversal or hierarchical management) Strong knowledge of RPA technologies, preferably Automation Anywhere Familiarity with data visualization tools (Power BI, Service Now query preferred) Experience with ServiceNow Experience in the pharmaceutical or healthcare industry Knowledge of process improvement methodologies (e.g., Six Sigma, Lean) Professional English proficiency (both written and verbal) Global exposure Skills Excellent communication (written and spoken), Problem-solving, Cross-functional coordination skills Analytical Reporting Crisis management Qualification Bachelor or Master degree in Computer Science, Information Technology, Business Administration, or related field ITIL Certification -preferred- RPA certifications (e.g., Automation Anywhere Certified Master RPA Professional) - preferred AWS Fundamentals - preferred Why choose us? Bring the miracles of science to life alongside a supportive, future-focused team. Discover endless opportunities to grow your talent and drive your career, whether it s through a promotion or lateral move, at home or internationally. Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks gender-neutral parental leave. Opportunity to work in an international environment, collaborating with diverse business teams and vendors, working in a dynamic team, and fully empowered to propose and implement innovative ideas.

Job title : Manager Quality Assurance Location Mumbai % Remote working and % of travel expected - 20% travel, working as per HO Mumbai policy Job type: Permanent About the job Our Team: This is external manufacturing dept. engaged in Quality compliance at contract manufacturing organization (CMO). Candidate has to ensure implementation and monitoring of the quality management systems at Sanofi EM sites as per cGMP and Sanofi GQD requirements in order to ensure the quality of products delivered to market with optimum resource utilization. To ensure local and country of export regulatory compliance requirements and provide stability data for products, manufactured, released and distributed for sale by External Mfg. To ensure proper analysis and documentation and product releases. Support Project management team for implementation of new products. (External Manufacturing) Actively manage the assigned CMOs to ensure supply of products at the right time and quantity, with acceptable quality, in full regulatory compliance. Main responsibilities: CGMP compliance at CMO & Release of products Ensure all Operational aspects of the manufacturing of pharmaceutical products at identified CMOs comply with the requirements of the Sanofi Quality directives and meet all relevant cGMP & regulatory requirements. Monitor and Ensure that all drug products are timely released in accordance with the registered specifications and are released to the market in accordance with local regulations. Ensure that coordinated contact is maintained with other functions within Sanofi namely Purchasing, Legal, Supply Chain, Drug Regulatory Affairs, and Marketing etc for timely operational compliance and release of product. Quality Agreements Maintain a valid QA agreement which is in line with the Global template clearly defining cGMP roles and responsibilities between Sanofi and the CMO s, for applicable products. Perform the required periodic review and negotiation with CMO and make recommendations for amendments to the agreement based on identified needs and issues. Audit Management Responsible for ensuring that Quality Audits of CMOs and suppliers of raw and packing materials are carried out as per allocation according to the defined frequencies and Annual calendar. All critical and major findings to be discussed with Quality Head and Head QO on timely manner for the appropriate action plan. Ensure closure for corrective and preventive action plans for audit findings and timely updated in QualiPSO. Product Technical Complaints Actively participate in the Product Technical complaint investigation with the CMO for the investigation of product technical complaints. Identification of appropriate CAPA and implemented timely manner at CMO. Closely coordinate with Hub for timely closer of PTC within timeline. Quality Management System Compliance Manage all Quality Issues (Deviations, complaints, OOS, recalls, counterfeit, stability failures, critical risk etc.) according to the Quality Management system defined as per EM SOP and Sanofi Global directives. Provide timely information to QMS on above quality event for registration in appropriate system e.g. QualiPSO. Actively participate in evaluation and defining CAPA / action plan/Investigations and agree with plan and its implementation time lines. Execute/Implement at CMO the task assigned in QualiPSO for relevant quality event, CC, investigation, CAPA, action item etc. Ensure investigations/actions items / CAPA s are correctly executed timely manner at CMO site as well as EM India organization as applicable. Ensure verification of implementation of identified CAPA at CMO during site Quality review visits. Ensure the compliance of the product through testing as per specification, change management, stability studies, deviation and investigation, OOS and market complaint systems. Responsible for assessing Quality trends through APQR s and driving Continuous improvement for processes and product quality performance. To ensure validations, qualifications at CMO site. Ensure all APQR are received timely manner as per APQR calendar and are assed with in timeline. Ensure all APQR are meeting requirement as per Sanofi SOP and Global directive. CMO Quality reviews Ensure all Quality reviews are conducted for the CMO s assigned as per the SQR calendar. Quality review visit reports are prepared timely manner and are discussed with Head QA for the observations and actions taken during the Site Quality reviews. Ensure the Product approved Dossier and Pharmacopeia are appropriately implemented for the products manufactured at assigned CMO. Identify the gaps and draw an action plan by discussion with head QA. Ensure implementation of action plan timely manner. Regulatory Authorities Inspection Ensure to maintain Quality and regulatory compliance of CMO allocated by On-Site Quality review as per planner. Ensure audit readiness at CMO for regulatory audits at CMO. Ensuring timely completion of the compliance to the local and export regulatory audits of the contract manufacturing sites. New Drug Product -Quality Evaluation Evaluate the new drug product sites for new product evaluation and follow up compliance to ensure the timelines of product launches. Review of product-quality dossiers and conclude on outcome and approval. Identify the gaps and draw an action plan by coordinating with CMO. Ensure implementation of action plan. Project Management To lead, participate, support the projects of technology transfer/Continuous Improvement projects for new products or existing products identified and allocated as per project Management. Ensure compliance to Sanofi Technology Transfer standards, procedures and applicable cGMP and regulatory registration (dossier) as required. Ensure smooth analytical and manufacturing transfer through close working with transferring site and receiving site. Ensure for timely feedback and updation on status of projects allocated to project management team. Conduct due diligence or cGMP audit of new site as a prospective sub contractor, evaluate & approve new product dossiers. Perform Quality Risk assessment To continuously evaluate the quality risks and escalate all potential quality issues and risks and initiate all actions as defined. To perform Quality Risk assessment as necessary for critical quality issues. Conduct investigation for the critical risk and timely feedback. Conduct the CMO risk ranking as per the frequency for the assigned CMO s. Timely discuss and align the Action plan for the improvement of CMO risk ranking with Head QA. Other Responsibilities Ensure all product related documents are collected and stored in Sanofi database to maintain complete product history. Reporting of KPI and submission of monthly report timely before 2nd of every month. Any other assignment allocated by manager depending upon the requirement. About you Experience : Minimum 10-15 year in Pharma formulations Soft skills : Communication, Analytical and strong logical orientation, Decision making, Networking Technical skills : Knowledge in quality function, work experience in Sterile products and non-sterile products manufacturing and compliance, Knowledge of Indian and International cGMP, regulatory and company s Global requirement in pharmaceutical Operations, Knowledge about QA, QC & Manufacturing Education : B pharm, M.Pharm / M.S. / M.Sc Languages : English, Hindi, Beware of Job Scams: Sanofi Fraud Notice: As you conduct your job search, please beware of the possibility that scammers may post fraudulent job openings or send fraudulent communications (email, SMS, WhatsApp or Messenger messages pretending to be from Sanofi) regarding potential job postings or offers in an attempt to encourage the job seeker to disclose financial or personal information. We do not make any payments to or ask candidates for any fees as part of the application process. In most cases you can expect to hear directly from a member of our recruiting team with a legitimate @sanofi.com email address, but you may receive communications from one of our recruiting partners as well. Consequently, you should always conduct research to ensure a posting and/or offer is legitimate and you should never provide personal or financial information unless you are certain that the request is legitimate. If you are concerned that an offer of employment with Sanofi might be a scam, please verify by searching for the posting on the Careers webpage

Project Manager - Office based/ Home based/ Bangalore/ Chennai/ Trivandrum ICON plc is a world-leading healthcare intelligence and clinical research organization. We re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. The Role: Project Manager - Laboratory IT and Data Integrity, Contract (12 months) Lead the planning and implementation of data integrity procedures and compliance working with a cross functional group within the organisation. Facilitate the definition of project scope, goals and deliverables Define project tasks and resource requirements. Develop full-scale cross-functional project plans. Plan and schedule project timelines Qualification of laboratory equipment and associated software Identify gaps in compliance across the laboratory in equipment and software qualification Develop and Manage Risk Mitigation processes when gaps identified Incorporate mitigation processes into standard operating procedures Train laboratory staff on new processes post qualification Track project deliverables using appropriate tools Provide direction and support to project team Communication of project progress to key stakeholders and senior management Quality assurance Constantly monitor and report on progress of the project to all stakeholders Present reports defining project progress, problems and solutions. Implement and manage project changes and interventions Desirable attributes: Laboratory experience (clinical / pharma / production) Experience with automated laboratory equipment interfaced to a networked LIMS Strong IT skills and knowledge In depth experience of working with and configuration of a LIMS system Experience in a laboratory or similar environment handling GXP data Knowledge of laboratory equipment and associated software desirable Knowledge of data integrity compliance advantageous Knowledge of lab accreditation processes and standards Experience of working with a quality management system including a robust CAPA process Standard operating procedure creation including document control system desirable. #LI-JS2 Benefits of Working in ICON: Our success depends on the knowledge, capabilities and quality of our people. That s why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development. At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future. ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. What ICON can offer you: Our success depends on the quality of our people. That s why we ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here . Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there s every chance you re exactly what we re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply