185 Ipr Jobs - Page 3

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About Thidiff About Clients Blogs Jobs Global Offices Contact Extended Team On-Site Team Offshore Team Technology Services Chrome Extension Development E-Commerce Services Magento Woocommerce Mobile Development Android App Development About Clients Blogs Jobs Global Offices Contact On-Site Team Offshore Team Chrome Extension Development Magento Woocommerce Android App Development Copyright 2025 ThiDiff All rights reserved

Jubilant Pharma Limited is a global integrated pharmaceutical company that offers a diverse range of products and services to customers worldwide. The business is structured into two primary segments: Specialty Pharmaceuticals and Generics & APIs. Under Specialty Pharmaceuticals, the company specializes in Radiopharmaceuticals, Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products. The Generics & APIs segment focuses on Solid Dosage Formulations & Active Pharmaceutical Ingredients. Jubilant Generics (JGL) serves as a wholly-owned subsidiary of Jubilant Pharma with Research & Development units located in Noida and Mysore, India. JGL operates manufacturing facilities in Mysore, Karnataka, and Roorkee, Uttarakhand, producing APIs and Dosage manufacturing, respectively. The Mysore manufacturing site, approved by USFDA, manufactures APIs targeting Lifestyle driven Therapeutic Areas such as CVS and CNS. It is a market leader in four APIs and among the top three players for three others. The Roorkee facility is a state-of-the-art site approved by multiple regulatory bodies including USFDA, Japan PMDA, UK MHRA, TGA, WHO, and Brazil ANVISA, focusing on a B2B model for EU, Canada, and emerging markets. Both manufacturing units are supported by a team of 500 research and development professionals based in Noida and Mysore. The R&D team is dedicated to developing new products in API, Solid Dosage Formulations of Oral Solid, Sterile Injectable, Semi-Solids Ointments, Creams, and Liquids. The in-house 80 Bed facility conducts all BA/BE studies and holds certifications from various global regulatory authorities. JGL's Regulatory Affairs & IPR professionals manage a unique portfolio of patents and product filings in both regulatory and non-regulatory markets. The company has shown consistent revenue growth, with INR 53,240 Million generated in the Financial Year 2018-19 compared to INR 39,950 Million in the Financial Year 2017-18. For more information about the organization, please visit www.jubilantpharma.com.,

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. Our business is organized into two segments - Specialty Pharmaceuticals and Generics & APIs. Jubilant Generics (JGL), a wholly-owned subsidiary of Jubilant Pharma, has Research & Development units in Noida and Mysore, India. JGL operates two manufacturing facilities in Mysore, Karnataka, and Roorkee, Uttarakhand, engaged in APIs and Dosage manufacturing, respectively. The Mysore manufacturing site, spread over 69 acres, is a USFDA approved facility producing APIs for global sales, with a focus on Lifestyle driven Therapeutic Areas like CVS and CNS. The Roorkee facility is state of the art, approved by multiple regulatory bodies, and operates on a B2B model for EU, Canada, and emerging markets. Backward-integrated manufacturing units are supported by around 500 research and development professionals based at Noida and Mysore. R&D activities include the development of new products in API and various dosage forms like Oral Solid, Sterile Injectable, Semi-Solids, Creams, and Liquids. In-house BA/BE studies are conducted at our 80-bed facility with global regulatory accreditations. JGL's Regulatory Affairs & IPR team ensures a unique portfolio of patents and product filings in regulatory and non-regulatory markets. The revenue of Jubilant Pharma has been on the rise, reaching INR 53,240 Million in the Financial Year 2018-19 compared to INR 39,950 Million in the Financial Year 2017-18. For more information about our organization, please visit www.jubilantpharma.com.,

Officer - Export & Import You will be responsible for further optimizing all processes related to Export, Import, Statutory Compliance, Customs clearance and legal requirements with the aim to improve overall customer satisfaction and avoid legal risks Export Logistics (Outbound Ensure accurate preparation of export documentation and timely execution of shipments, with a sound understanding of commercial procedures Track the status of post-export shipping documents to ensure proper follow-up and closure Submit export documents to the bank promptly and monitor their progress until the AD Bank issues a reference Manage documentation workflows and negotiate terms under Letters of Credit Ensure strict compliance with all statutory regulations governing export shipments Coordinate with third-party inspection agencies (e.g., SGS, Bureau Veritas) for export-related inspections.Handle specialized transactions, including deemed exports, third-country, and cross-country shipments Demonstrate expertise in managing both preferential (REX, AIFTA, SAFTA) and non-preferential Certificates of Origin Manage re-export procedures for scenarios such as sales returns, rejections, repairs, and post-exhibition returns Secure GR Waivers efficiently and ensure timely closure of export obligations Handle exports under various license schemes and ensure compliance and closure Control and negotiate freight costs for optimal value Build and maintain strong relationships with customs house agents (CHA), freight forwarders, shipping lines, customs officials, insurance agents, and other stakeholders Maintain accurate and up-to-date digital records of all export activities Import Logistics (Inbound Oversee import operations from multiple international suppliers and countries Ensure timely clearance of imports under applicable schemes such as MRP, BIS, IPR, WPC, SIMS, and PIMS Manage the import of second-hand machinery in compliance with applicable norms.Handle temporary import procedures for repairs or exhibitions. Manage imports into Free Trade and Warehousing Zones (FTWZ) Administer high sea sale transactions effectively.Coordinate merchandise trade transactions and ensure smooth processing Collaborate with shippers, CHAs, freight forwarders, shipping lines, ports, and CFS operators to facilitate timely customs clearance Monitor the use of import licenses and ensure complete utilization and closure within defined timelines. To succeed, you will need Experience Requirements: Proven expertise in managing end-to-end operational processes associated with export and import activities 5 to 7 years of hands-on experience in export-import functions, specifically within the manufacturing or trading sectors.Exceptional communication skills, both verbal and written Skilled in planning, managing, and evaluating logistics operations through effective coordination with internal teams, suppliers, logistics partners, transport companies, Customs authorities, and customers Ability to develop and implement best practice logistics strategies, policies, and procedures to enhance both operational efficiency and financial outcomes. Knowledge Requirements In-depth knowledge of Indian Customs regulations, RBI guidelines, marine insurance procedures, and port/shipping operations Familiarity with Free Trade Agreements (FTAs), trade barriers, and restricted country regulations.Comprehensive understanding of logistics workflows, developed through previous roles in logistics, supply chain management, or transportation Expertise in technical and statutory regulations governing import/export and customs compliance Proficiency in enterprise systems such as BPCS and SAP is an added advantage Advanced skills in Microsoft Excel for data analysis, and strong command of PowerPoint for impactful presentations. Educational Requirements A Bachelor s degree in any discipline from a recognized university Supplemented with a Management Degree or Diploma specializing in Import-Export operations or International Trade. In return, we offer Culture of trust and accountability Lifelong learning and career growth Innovation powered by people Comprehensive compensation and benefits Health and well-being Job location Pune Contact information Talent Acquisition Team: Mahesh Deshmukh Uniting curious minds Behind every innovative solution, there are people working together to transform the future. With careers sparked by initiative and lifelong learning, we unite curious minds, and you could be one of them.

Design, development and testing of components / modules in TOP (Trade Open Platform) involving Spark, Java, Hive and related big-data technologies in a datalake architecture Contribute to the design, development and deployment of new features new components in Azure public cloud Contribute to the evolution of REST APIs in TOP enhancement, development and testing of new APIs Ensure the processes in TOP provide an optimal performance and assist in performance tuning and optimization Release Deployment Deploy using CD/CI practices and tools in various environments development, UAT and production and follow production processes. Ensure Craftsmanship practices are followed Follow Agile at Scale process in terms of participation in PI Planning and follow-up, Sprint planning, Back-log maintenance in Jira. Organize training sessions on the core platform and related technologies for the Tribe / Business line to ensure the platform evolution is continuously updated to relevant stakeholders Around 4-6 years of experience in IT industry, preferably banking domain Expertise and experience in Java (java 1.8 (building API, Java thread, collections, Streaming, dependency injection/inversion), Junit, Big-data (Spark, Oozie, Hive) and Azure (AKS, CLI, Event, Key valut) and should have been part of digital transformation initiatives with knowledge of Unix, SQL/RDBMS and Monitoring Development experience in REST APIs Experience in managing tools – GIT/BIT Bucket, Jenkins, NPM, Docket/Kubernetes, Jira, Sonar Knowledge of Agile practices and Agile@Scale Good communication / collaboration skills

About IndiaFilings: IndiaFilings is Indias premier platform offering end-to-end services in business registration, GST, Income Tax filing, Trademark, and legal compliance. Our mission is to simplify business processes for entrepreneurs and professionals through expert services and technology. Role Summary We are seeking a qualified Lawyer with a flair for Content Writing to join our legal team. The ideal candidate will be responsible for creating high-quality, legally accurate, and engaging content tailored to entrepreneurs, businesses, and professionals across India and the UAE. This includes writing articles, website content, legal documents, knowledge base guides, FAQs, and more. Key Responsibilities Research and write informative, SEO-optimized articles and guides on topics including Company Law, Taxation, Intellectual Property, Contract Law, Business Compliance, and Startup Laws. Draft standard legal documents, formats, and client communication templates. Simplify complex legal topics into user-friendly content for entrepreneurs and business owners. Collaborate with the Marketing and Product teams to create landing pages, email campaigns, and product explainers. Ensure all content is legally accurate and updated as per the latest laws, rules, and notifications. Create training material and knowledge base documentation for internal and external use. Nice to Have Prior experience in working with legal-tech or compliance startups. Exposure to content tools like Grammarly, WordPress, or SurferSEO. Experience writing for client-facing portals or knowledge base platforms. Perks & Benefits Opportunity to work with a dynamic legal-tech platform. Exposure to practical business and legal scenarios. There is any one interested please contact me Hr Geetanjali- 8657498073. Company Address- Ghansoli MBP Aurum Proptech 6th floor Indiafilings Pvt Ltd.

Key Responsibilities: • Coordinate with engineering teams to gather inventive ideas. Perform basic prior art and patent searches. Support the Legal/IPR team in compliance and internal audits related to patents and trademarks. • Maintain documentation and filing records as per regulatory requirements. • Follow up with our third-party vendors in getting the patents filed on right time. • Post filing follow up activities check/ follow up on patent filing number Who Can Apply: Final-year students or recent graduates from Law graduates with interest in Intellectual Property. Strong interest in legal research, patent law, and innovation management. Excellent communication and documentation skills. Career Growth Path: This role is your stepping stone into the IPR & Patent Research domain. Based on performance, youll have the opportunity to transition into a full-time role, where your career can grow through: • Exposure to patent analytics, filing strategies, and innovation portfolio management • Training in national and international IP laws • Long-term roles such as IPR Analyst, Patent Coordinator, or IP Strategy Consultant.

As a Senior Chemist in the Pharma Manufacturing Industry located in Vatva, Ahmedabad, your role will involve utilizing your M.Sc. in Organic Chemistry and 5 to 8 years of experience in API / Intermediates manufacturing within the pharmaceutical sector. Your responsibilities will include hands-on experience in the synthesis of APIs and intermediates, conducting literature searches using platforms such as SciFinder, Chemical Abstracts, Free Patent Online, and Journals. You will be involved in feasibility studies, route selection for synthesis, multi-step synthesis, yield improvement, and cost reduction strategies. Additionally, you will be responsible for tasks such as extraction, purification, distillation, lab validations, process development with strong documentation including Tech reports, process safety reports, and cost sheets. Furthermore, you will lead technology transfer from the laboratory to kilo lab and plant scale, while coordinating with IPR, Regulatory Affairs, and QA departments. Proficiency in tools like Chemdraw / Chemsketch is essential for this role. Please note that only male candidates from the Pharma Manufacturing Industry will be considered for this position. If you are seeking a challenging full-time, permanent role that requires your expertise in organic chemistry and pharmaceutical manufacturing, we look forward to receiving your application. With Regards, Himani(HR) 9377165778,

The School of Law (SoL), RV University, aims to provide quality legal education in India and integrates seamlessly with the existing schools of RVU, which focus on liberal arts and sciences, design, economics, business, and computer science and engineering. Our students benefit from an interdisciplinary approach, examining intersections between law and fields such as business, economics, social sciences, technology, and public policy. SoL offers B.A. LL.B., B.B.A. LL.B., and LL.M. (IPR & General) programs that comply with the BCI & UGC Rules along with opportunities for research and participation in student clubs and societies. This is a full-time on-site role located in Bengaluru for a Faculty of Law position, open to Professor, Associate Professor, and Assistant Professor levels. The selected candidate will be responsible for teaching undergraduate and postgraduate law courses, conducting research, and contributing to curriculum development. Additional administrative duties include mentoring students, participating in faculty meetings, and engaging in academic and professional service within the university. Qualifications: - Ph.D. in Law (preferred) - Expertise in Law, with a specialization in Corporate Law/Information & Technology Law/IPR/ADR - Experience and skills in Research (Scopus, Wos, and Sci) and Teaching - Excellent written and verbal communication skills - Ability to work collaboratively in an academic environment - Prior academic experience in teaching and research (preferred) You are requested to apply by sharing your detailed resume by email mentioning the position in the subject line, along with all supporting documents to recruitments@rvu.edu.in The online interviews will be held online soon, once shortlisted by the selection panel.,

Responsibilities & Key Deliverables Liaison with Platform team and VES COE s for ensuring Program defined TCP are meeting the Targets L1 to L4 Timeplan preparation and monitoring. Ensure control of timeline revisions are updated and communicated to respective COE s Project Risk monitoring and escalation to GPH s/Delivery heads/Vertical Heads/President Gateway deliverables - Activities monitoring and closure, Critical path identification. Represent respective GPH s in NPQ meetings Software releases tracking in line with MPDS Gateway CMTCP monitoring Timeline and Performance Circulate Project MIS report to leadership team Maintain and publish project specific - single issue list and follow-up for closure Support for new Program scope finalization and Budget estimation Support for E-BOM release and build intent sign off for respective builds Support for Parts tracking for vehicle build requirement in co-ordination with CDMM Monitor supplier end development activities and escalate critical concerns Monitor and publish Validation, RGA, Plant specific concerns reports to internal team Investment and Material Cost to be monitored and communicate to central budget management team and escalate for deviation IMCR, Field concerns - consolidation and monitoring for implementation Monitor and manage resource utilization Standardization - within projects Support for NDA/PR-PO/Contract/ Service agreement preparation, IPR Registration and Approval tracking Knowledge Management & lessons learnt deployment Experience 5-17 Years Industry Preferred Qualifications BE/B Tech Electrical Engineering BE/B Tech Electrical and Electronics Engineeing BE/B Tech Automobile engineering BE/B Tech Mechatronics Engineering General Requirements Very Good Vehicle system knowledge and E&E agregates in the vehicle- Distribution system,Starting & Charging system,Lighting system and swtichtes Expertise in WH & vehicle trouble shooting Knowledge in Catia V5, Capital Harness is added advantage Program management skills Basic level knowledge in Vehicle electronics & In Vehilce netwroking systems - Body contorl module, ABS/ESP,Airbag &Infotainment, Communicaiton protocols like CAN & LIN

Boudhik IP is looking for Senior Attorney to join our dynamic team and embark on a rewarding career journey. Intellectual Property (IP) attorneys, also known as intellectual property lawyers or patent attorneys, specialize in the area of law that deals with protecting the rights of individuals and businesses in their creations or inventions. IP attorneys play a crucial role in helping clients navigate the legal landscape related to intellectual property, which includes patents, trademarks, copyrights, and trade secrets. Here is a general job description for IP attorneys : Legal Consultation : Provide legal advice and guidance to clients on intellectual property matters. Assist clients in understanding their rights and options concerning patents, trademarks, copyrights, and trade secrets. Patent Prosecution : Prepare and file patent applications with the appropriate patent offices. Work closely with inventors and technical experts to understand the details of inventions. Respond to patent office actions and communicate with patent examiners. Trademark and Copyright Registration : Assist clients in registering trademarks and copyrights to protect their brands and creative works. Conduct searches to ensure the availability of trademarks and copyrights. IP Litigation : Represent clients in intellectual property disputes, including patent, trademark, and copyright litigation. Draft legal documents such as complaints, responses, and motions. Due Diligence : Conduct intellectual property due diligence in business transactions, mergers, and acquisitions. Assess the intellectual property portfolio of a client or target company. Contract Review and Drafting : Review and draft agreements related to intellectual property, such as licensing agreements, technology transfer agreements, and non - disclosure agreements. Client Counseling : Counsel clients on strategies for protecting and enforcing their intellectual property rights. Educate clients on IP laws and regulations. Legal Research : Stay abreast of changes in intellectual property laws and regulations. Conduct legal research to support client cases and provide accurate advice. Alternative Dispute Resolution : Participate in alternative dispute resolution processes, such as arbitration or mediation, to resolve intellectual property disputes. Client Advocacy : Advocate for clients before government agencies, such as the United States Patent and Trademark Office (USPTO) or the World Intellectual Property Organization (WIPO).

" 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 ",

Responsibilities & Key Deliverables Liaison with Platform team and VES COE s for ensuring Program defined TCP are meeting the Targets L1 to L4 Timeplan preparation and monitoring. Ensure control of timeline revisions are updated and communicated to respective COE s Project Risk monitoring and escalation to GPH s/Delivery heads/Vertical Heads/President Gateway deliverables - Activities monitoring and closure, Critical path identification. Represent respective GPH s in NPQ meetings Software releases tracking in line with MPDS Gateway CMTCP monitoring Timeline and Performance Circulate Project MIS report to leadership team Maintain and publish project specific - single issue list and follow-up for closure Support for new Program scope finalization and Budget estimation Support for E-BOM release and build intent sign off for respective builds Support for Parts tracking for vehicle build requirement in co-ordination with CDMM Monitor supplier end development activities and escalate critical concerns Monitor and publish Validation, RGA, Plant specific concerns reports to internal team Investment and Material Cost to be monitored and communicate to central budget management team and escalate for deviation IMCR, Field concerns - consolidation and monitoring for implementation Monitor and manage resource utilization Standardization - within projects Support for NDA/PR-PO/Contract/ Service agreement preparation, IPR Registration and Approval tracking Knowledge Management & lessons learnt deployment Experience 5 to 17 Years Industry Preferred Qualifications BE/B Tech Electrical Engineering BE/B Tech Electrical and Electronics Engineeing BE/B Tech Automobile engineering BE/B Tech Mechatronics Engineering General Requirements Very Good Vehicle system knowledge and E&E agregates in the vehicle- Distribution system,Starting & Charging system,Lighting system and swtichtes Expertise in WH & vehicle trouble shooting Knowledge in Catia V5, Capital Harness is added advantage Program management skills Basic level knowledge in Vehicle electronics & In Vehilce netwroking systems - Body contorl module, ABS/ESP,Airbag &Infotainment, Communicaiton protocols like CAN & LIN

Position: Research Associate/Research Scientist Locations: Manesar, Gurugram, Haryana Experience: 4-8 Years Qualification Masters in Pharmacy (Pharmaceutics). Department IPR Formulation Responsibilities: Preparing initial PPAR reports (IP landscape) for majorly US, Europe, & India markets. Preparing IP clearances / FTOs for the products. Preparing file wrapper summaries of relevant patents. Trade dress clearances. Monthly/Weekly/daily tracking of updates (USFDA & OB), important patent applications, new patent publications. Suggesting Patent invalidation/NI options for early entry for ANDA. Identification of potential drug products for Pipeline. Hands on searching equivalents, calculating expiries for providing entry dates for ROW countries. Patent drafting and prosecution. Knowledge and understanding of drug formulation concepts. Knowledge and understanding of Patent laws of Major countries. Knowledge and understanding of drug regulatory approval pathway. Good verbal and written communication skill. Good knowledge of Microsoft word and Microsoft excel. Hands on experience of Patent related databases such as Scifinder, Derwent, Orbit, Ark, Patent Office Sites of various jurisdictions.

Job Title: Client Relationship Executive IP Services (Work From Home) Location: Coimbatore, Madurai, Bangalore (Remote – Work from Home) Experience: 2 to 3 years Industry: Legal / Intellectual Property (Trademark, Copyrights, Patents) Job Summary: We are looking for a dedicated and detail-oriented Client Relationship Executive to join our Intellectual Property team. The ideal candidate will be responsible for managing client relationships, addressing inquiries, and ensuring smooth coordination related to trademark registrations, renewals, copyrights, patents , and related IP services. This role is fully remote and open to candidates based in Coimbatore, Madurai, or Bangalore . Key Responsibilities: Act as the primary point of contact for clients, addressing queries related to trademarks, copyrights, patents, and renewals. Maintain regular communication with clients to provide status updates and resolve concerns. Coordinate with legal and IP teams to ensure accurate and timely execution of client requests. Ensure proper documentation and follow-up for filing, renewals, and IP compliance deadlines. Educate clients on IP procedures, timelines, and legal formalities involved in trademark and patent filings. Build long-term relationships with clients by understanding their business needs and offering tailored solutions. Maintain and update client records and case status on internal tools and CRM systems. Provide assistance in client onboarding and conduct post-service follow-ups to ensure satisfaction. Required Skills and Qualifications: Bachelor’s degree in Law, Business Administration, or a related field. 2 to 3 years of experience in client servicing, preferably in the legal or intellectual property domain. Strong understanding of IP-related services such as trademark registration and renewal, copyright filing, and patents . Excellent communication skills (written and verbal) in English. Highly organized, detail-oriented, and capable of managing multiple client accounts. Proficient in MS Office, CRM tools, and virtual collaboration platforms. Self-motivated and comfortable working remotely. Preferred Skills: Prior experience working in an IP law firm or IP consultancy. Basic knowledge of IP laws and procedures in India. Ability to speak regional languages (Tamil/Kannada) is a plus.

Hi, We are having an opening for Senior Executive-IP litigation at our Mumbai location. Job Summary : Executive role in IP litigations FTO searches & evaluation reports, identifying IP risks pre-PIF assessment, providing IP litigation support to various internal stakeholders. Areas Of Responsibility : FTO searches & preparing evaluation reports Pre-PIF assessments Timely support to Portfolio, Business Development, R & D, PMO, and Regulatory teams New Product Opportunity Identification - based on IP scenarios Monitoring of IP updates, Competitive Intelligence and regulatory developments Educational Qualification : Master of Pharmacy or M.S. or M. Tech. (Pharmaceutics or Chemistry preferred) Specific Certification : P.G. Diploma in Patents Law (preferred) Skills : Sound understanding of IP dynamics, technical skills, Good communication skills, Team player, Agility & adaptability Experience : Around 4-5 years of relevant experience in Formulation- IP domain

Arctic Invent is a leading intellectual property firm dedicated to providing innovative solutions to protect the intellectual property rights of our clients. Specializing in patent, trademark, and copyright services, our commitment to excellence has made us a trusted partner for businesses and inventors worldwide. We are now inviting applications from enthusiastic individuals to join our team as Manager of CEO Operations at our Noida-based office. As the Manager of CEO Operations, you will play a crucial role in supporting the CEO in daily operations, ensuring seamless communication and efficient processes. Your responsibilities will include facilitating communication between the CEO and different departments, monitoring project timelines, updating internal systems, and ensuring data accuracy. You will also be expected to utilize tools and technology efficiently to streamline tasks, maintain positive relationships with clients, and handle tasks that may arise unexpectedly to keep operations running smoothly. A typical day in this role will involve reviewing emails, updating project statuses, coordinating with different teams, jumping on calls with clients or team members, and engaging in structured tasks and dynamic problem-solving to ensure operations stay on track. Requirements for this position include an MBA/PGDM in any discipline, 2+ years of experience in client management or data management, immediate joiners will be given preference, working knowledge of MS Excel, data management, or MIS experience is desirable, IPR experience will be an added advantage, detail-oriented with a high level of accuracy, analytical mindset and problem-solving skills, ability to work collaboratively in a team environment, ability to perform under pressure and manage multiple priorities, excellent attention to detail and follow-through, good emailing etiquettes, self-motivated and able to perform with minimal supervision, and ability to deliver to deadlines and follow up on commitments. Benefits of joining Arctic Invent include a competitive salary, structured training and mentorship program, opportunities for career growth within the firm, and a vibrant and inclusive workplace culture. Arctic Invent is an equal opportunity employer, celebrating diversity and committed to fostering an inclusive work environment for all team members. For more information, please visit our website at https://www.arcticinvent.com.,

Jubilant Pharma Limited is a global integrated pharmaceutical company that offers a diverse range of products and services to customers worldwide. The business is structured into two key segments: Specialty Pharmaceuticals and Generics & APIs. In the Specialty Pharmaceuticals segment, the company specializes in Radiopharmaceuticals, Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products. The Generics & APIs segment focuses on Solid Dosage Formulations & Active Pharmaceutical Ingredients. Jubilant Generics (JGL) is a wholly-owned subsidiary of Jubilant Pharma, with Research & Development units located in Noida and Mysore, India. JGL operates manufacturing facilities in Mysore, Karnataka, and Roorkee, Uttarakhand, dedicated to APIs and Dosage manufacturing. The Mysore manufacturing site, spread over 69 acres, is USFDA approved and produces APIs for global distribution, with a focus on Lifestyle driven Therapeutic Areas such as CVS and CNS. The Roorkee facility is a state-of-the-art site approved by multiple regulatory bodies including USFDA, Japan PMDA, UK MHRA, TGA, WHO, and Brazil ANVISA, catering to B2B markets in EU, Canada, and emerging markets. Backward-integrated manufacturing units are supported by a team of 500 research and development professionals based in Noida and Mysore. The R&D team focuses on developing new products in API, Solid Dosage Formulations, Sterile Injectable products, Semi-Solids like Ointments, Creams, and Liquids. The company conducts all BA/BE studies in-house at an 80 Bed facility with global regulatory accreditations. JGL's Regulatory Affairs & IPR professionals manage a unique portfolio of patents and product filings for regulatory and non-regulatory markets. Jubilant Pharma has witnessed consistent revenue growth, with revenue reaching INR 53,240 Million in the Financial Year 2018-19, compared to INR 39,950 Million in the Financial Year 2017-18. For more information about the organization, please visit www.jubilantpharma.com.,

You will be working at Jubilant Pharma Limited, a global integrated pharmaceutical company that offers a wide range of products and services across different geographies. The business is organized into two segments: Specialty Pharmaceuticals and Generics & APIs. Jubilant Generics (JGL) is a wholly-owned subsidiary of Jubilant Pharma with Research & Development units in Noida and Mysore, India. JGL operates manufacturing facilities in Mysore, Karnataka, and Roorkee, Uttarakhand, focusing on APIs and Dosage manufacturing. The Mysore manufacturing site, spread over 69 acres, is USFDA approved and manufactures APIs targeting Lifestyle driven Therapeutic Areas such as CVS and CNS. The Roorkee facility is a state-of-the-art site approved by multiple regulatory bodies including USFDA, Japan PMDA, UK MHRA, TGA, WHO, and Brazil ANVISA, primarily focusing on a B2B model for EU, Canada, and emerging markets. Both manufacturing units are supported by around 500 research and development professionals in Noida and Mysore, working on developing new products in API, Solid Dosage Formulations, Sterile Injectable, Semi-Solids Ointments, Creams, and Liquids. The R&D facility also conducts BA/BE studies in-house and has global regulatory accreditations. JGL's Regulatory Affairs & IPR professionals focus on maintaining a unique portfolio of patents and product filings in regulatory and non-regulatory markets. Jubilant Pharma's revenue has been consistently increasing, reaching INR 53,240 Million during the Financial Year 2018-19 compared to INR 39,950 Million in the Financial Year 2017-18. Your responsibilities will include managing Stability Chambers, handling Stability Samples, loading & withdrawing Stability samples, storage, and destruction of samples after testing, compiling Stability reports, timely analysis of stability samples, investigation of deviations, incidents, OOS & OOT results, recording analytical data, preparation & review of SOPs, self-auditing, adherence to SOPs, STPs, GTPS, and cGMP/GLP compliance. For more information about the organization, please visit www.jubilantpharma.com.,

Profile Position: Secretary in Patent Department. Exposure and experience in the e-filing module of the Indian Patent office Desired Skills and Experience: - 1. Experience of around 2-6 years 2. Experience in an IPR law firm or in the IPR department of other organizations. Filing of applications, formality documents, responses, post-grant documents etc. 3. Education: Qualification: Graduation 4. Good academic record and analytical skills 5. Confident; sound communication skills; ability to coordinate with clients and professional personnel within the firm; good relationship skills KS Partners is one of the leading IP Law firms in India with offices in Gurgaon, Bangalore, Mumbai, Chennai, Pune and Hyderabad. In terms of its practice, KS provides services across all aspects of Intellectual Property rights including patents, plant varieties, designs, trademarks, copyright, geographical indications, trade secrets and related matters. Founded in 1664, today it has approx. 400 people and is amongst the top five IP firms in India.

As a Senior Chemist in the Pharma Manufacturing Industry based in Vatva, Ahmedabad, you will be responsible for the synthesis of APIs and intermediates. Your role will involve conducting feasibility studies, selecting synthesis routes, and implementing multi-step synthesis processes to improve yield and reduce costs. You will utilize your expertise in conducting literature searches using platforms such as SciFinder, Chemical Abstracts, and Free Patent Online, as well as referring to various journals. Additionally, you will be involved in extraction, purification, and distillation processes, along with conducting lab validations. Strong documentation skills are essential for this role, including the preparation of technical reports, process safety reports, and cost sheets. You will also play a key role in technology transfer activities from the laboratory to kilo lab and plant scale. Collaboration with departments such as IPR, Regulatory Affairs, and QA will be crucial in ensuring compliance and quality standards are met. Proficiency in tools like Chemdraw and Chemsketch will be beneficial for this role. Please note that this position is open to male candidates with a background in the Pharma Manufacturing Industry. If you have a Master's degree in Organic Chemistry and possess 5 to 8 years of relevant experience in API and intermediates manufacturing within the Pharma industry, we encourage you to apply for this full-time, permanent position. For further details or to express your interest, please contact Himani (HR) at 9377165778. Thank you.,

Ways of Working - Full time Office role on hybrid mode (Bangalore) About Swiggy Swiggy is India s leading on-demand delivery platform with a tech-first approach to logistics and a solution-first approach to consumer demands. With a presence in 500+ cities across India, partnerships with hundreds of thousands of restaurants, an employee base of over 5000, a 2 lakh+ strong independent fleet of Delivery Executives, we deliver unparalleled convenience driven by continuous innovation. Built on the back of robust ML technology and fuelled by terabytes of data processed every day, Swiggy offers a fast, seamless and reliable delivery experience for millions of customers across India. From starting out as a hyperlocal food delivery service in 2014, to becoming India s leading on-demand convenience platform today, our capabilities result not only in lightning-fast delivery for customers, but also in a productive and fulfilling experience for our employees. Roles and Responsibilities: Draft, review and negotiate a variety of commercial agreements, Nondisclosure Agreements, Supply Agreements, Master Service Agreements, Statement of Works, IPR related documents and other legal documents. Focus on service agreements, licensing agreements, vendor contracts, advertising, endorsement, marketing agreements, sponsorship agreements, NDAs etc. Support new business initiatives, project work with project teams to ensure legal evaluation and timely compliance with all conditions precedent and other contractual obligations. Research on applicable regulatory laws and prepare in-house preliminary opinions. Assist in reviewing print, social media and other media advertisements and marketing communications to ensure legal compliance. Provide guidance and assistance on drafting and reviewing different policies and terms and conditions relating to offers, business and our services. Desired skills: Transactional drafting, negotiation and advisory experience on different commercial transactions gained at a leading law firm and/or in-house at a multinational corporation The role requires the individual to be well skilled in contract analysis and working knowledge of the fundamental legal provisions of commercial contracts. Excellent attention to details, ability to analyze and assess business processes, spot issues and propose/implement solutions. Ability to function autonomously yet communicate laterally and upwardly with ease. Strong legal and business judgment. Excellent written and oral communication and interpersonal skills to effectively communicate and coordinate complex issues and projects with diverse levels of management and employees. Ready and willing to take up new projects and work independently with minimal supervision and take responsibility. Prioritize and manage work load effectively, recognizing the quick turn-around requirements. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, disability status, or any other characteristic protected by the law.

Jubilant Pharma Limited is a global integrated pharmaceutical company that offers a wide range of products and services to customers across various geographies. The business is organized into two segments: Specialty Pharmaceuticals and Generics & APIs. Specialty Pharmaceuticals segment includes Radiopharmaceuticals, Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products. Generics & APIs segment comprises Solid Dosage Formulations & Active Pharmaceutical Ingredients. Jubilant Generics (JGL) is a wholly-owned subsidiary of Jubilant Pharma with Research & Development units in Noida and Mysore, India. It operates two manufacturing facilities in Mysore, Karnataka, and Roorkee, Uttarakhand, focusing on APIs and Dosage manufacturing. The Mysore manufacturing site, spread over 69 acres, is a USFDA approved facility catering to global sales with a portfolio concentrating on Lifestyle-driven Therapeutic Areas like CVS, CNS. The Roorkee facility is state-of-the-art and approved by multiple regulatory bodies including USFDA, Japan PMDA, UK MHRA, TGA, WHO, and Brazil ANVISA, following a B2B model for EU, Canada, and emerging markets. Both manufacturing units are backward-integrated and supported by approximately 500 research and development professionals in Noida and Mysore. R&D efforts include developing new products in API, Solid Dosage Formulations, Sterile Injectable, Semi-Solids Ointments, Creams, and Liquids. JGL's Regulatory Affairs & IPR professionals maintain a unique portfolio of patents and product filings in regulatory and non-regulatory markets. Jubilant Pharma's revenue has been consistently growing, reaching INR 53,240 Million during the Financial Year 2018-19 compared to INR 39,950 Million in the Financial Year 2017-18. For more information about the organization, please visit www.jubilantpharma.com.,

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. The business is organized into two segments: Specialty Pharmaceuticals and Generics & APIs. Jubilant Generics (JGL), a wholly-owned subsidiary of Jubilant Pharma, operates Research & Development units in Noida and Mysore, India. The company has two manufacturing facilities - one in Mysore, Karnataka, and another in Roorkee, Uttarakhand - engaged in the production of APIs and Dosage manufacturing. The Mysore manufacturing location, spread over 69 acres, is a USFDA approved site specializing in manufacturing APIs for Lifestyle driven Therapeutic Areas such as CVS and CNS. It is a market leader in four APIs and among the top three players for three other APIs in its portfolio. On the other hand, the Roorkee facility is a state-of-the-art site approved by multiple regulatory bodies including USFDA, Japan PMDA, UK MHRA, TGA, WHO, and Brazil ANVISA. This facility focuses on a B2B model for EU, Canada, and emerging markets. Both manufacturing units are supported by approximately 500 research and development professionals based at Noida and Mysore. The R&D team works on developing new products in API, Solid Dosage Formulations of Oral Solid, Sterile Injectable, Semi-Solids Ointments, Creams, and Liquids. Additionally, all BA/BE studies are conducted in-house at an 80-bed facility with approvals from various regulatory authorities. JGL's Regulatory Affairs & IPR professionals ensure a unique portfolio of patents and product filings in regulatory and non-regulatory markets. Jubilant Pharma's revenue has shown a constant increase, reaching INR 53,240 Million in the Financial Year 2018-19 compared to INR 39,950 Million in the Financial Year 2017-18. For more information about the organization, please visit www.jubilantpharma.com.,