282 Ipr Jobs - Page 4

About Our Client: Our client is a tech-enabled outsourcing platform that integrates AI with human expertise to deliver exceptional customer experiences. Their servicesranging from telecalling to sales and supportleverage automation and trained professionals to drive efficiency, reduce costs, and scale business growth across industries. Designation: Legal Manager Location: Noida Experience: 8 - 10 Years Qualification: Bachelors or Masters in Law preferred About the role: We are looking for a proactive and detail-oriented Legal Manager to support our growing business by managing day-to-day legal operations, contracts, and compliance matters. This role requires a commercially savvy legal profes...

Responsibilities - - Should be persuasive and have strong business acumen. - Hands-on experience with the strategies involved in scaling up business from Knowledge of IPR (Basic). - Should have updated cadences to develop a framework to bring clients. - Reaching out to potential clients through email, LinkedIn, and phone calls and scheduled meetings with the Partners and another source of Social media. - Conduct initial conversations to understand the legal needs and fulfill the same. - Use Innovative writing techniques and updated cadences on developed a framework to bring clients on the table and onboard from various industries including big giants. Requirements:- - Bachelor's degree in bu...

Role & responsibilities We are seeking a highly skilled and detail-oriented Intellectual Property Rights (IPR) Specialist to support in overseeing and managing the company's intellectual property portfolio. The ideal candidate will have a strong understanding of patents, trademarks, copyrights and trade secrets, with the ability to protect and enforce IP rights globally. You will work closely with the legal team, product development, and R&D departments to identify, protect, and manage the company's intellectual assets. Preferred candidate profile - Immediate Joiner

Technical Skills: - Experience to prosecute trademark applications (including post registration prosecution such as assignments etc.) and oppositions single handedly. - Managing Trademark Portfolio of clients; docketing and routine follow ups with clients. - Experience of undertaking Trademark searches and providing opinion to clients. - Experience of providing opinion on contentious / dispute matters involving trademarks. - Experience of attending official hearings in Registry for both Trademark application and opposition proceedings. - Experience of following up with Trademarks Registries for disposal of requests filed in both pre-registration and post registration stages. - Experience in ...

JOB PURPOSE: The position will cater to the increasing requests for patent check (Pre-screening/FTO/Landscape/Combination Portfolio) from different regions and will assist the team to perform thorough patent check for advancing projects that are bound by strict timelines. There are number of projects and required manager level position to guide team and also responsible for the development of focused new portfolio. JOB RESPONSIBILITIES: Freedom to operate analysis . Patent searches using various databases Preparation of patent landscape Infringement analysis of formulation/recipe proposed by R & D and review of critical patents. Pre-screening patent report Identify blocking patents Design IP...

The ideal candidate for this position should possess a Graduate degree in L.L.B with 2-5 years of relevant experience. As part of the role, you will be responsible for demonstrating excellent drafting skills in the preparation of civil suits, contracts, notices, and deeds. Additionally, you will handle recovery cases and litigation related to N.I. Act, Trade Mark Matter, and IPR. Furthermore, you will be required to appear in court and coordinate with lawyers effectively. Strong presentation and communication skills are essential for this role. The location of this job is in Gurgaon.,

Jubilant Pharma Limited offers a diverse range of products and services to customers globally through its two key segments - Specialty Pharmaceuticals and Generics & APIs. As a wholly-owned subsidiary of Jubilant Pharma, Jubilant Generics (JGL) plays a crucial role in the organization's operations. JGL has Research & Development units in Noida and Mysore, along with manufacturing facilities in Mysore, Karnataka, and Roorkee, Uttarakhand. The Mysore facility, spread over 69 acres, is a USFDA approved site specializing in the manufacturing of APIs that cater to global sales. The API portfolio primarily focuses on Lifestyle driven Therapeutic Areas such as CVS and CNS, emphasizing complex and n...

As a Senior Chemist in the Pharma Manufacturing Industry located in Vatva, Ahmedabad, your primary responsibility will be to utilize your M.Sc. in Organic Chemistry along with 5 to 8 years of experience in API/Intermediates manufacturing to contribute significantly to the organization. Your role will involve hands-on experience in synthesizing APIs and intermediates, conducting literature searches using platforms such as SciFinder, Chemical Abstracts, Free Patent Online, and Journals. You will be responsible for feasibility studies, route selection for synthesis, multi-step synthesis, yield improvement, and cost reduction strategies. Additionally, you will be involved in extraction, purifica...

Jubilant Pharma Limited is a global integrated pharmaceutical company that offers a diverse range of products and services to customers worldwide. The business is organized into two segments: Specialty Pharmaceuticals, which includes 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, with Research & Development units in Noida and Mysore, India. JGL operates two manufacturing facilities in Mysore, Karnataka, and Roorkee, Uttarakhand, specializ...

Company Description BUG Aeterium is a fast-evolving workforce solutions startup on a mission to simplify how businesses grow, expand, and operate across borders. As we scale, were looking for a sharp, curious, and business-minded Legal Intern to help us lay the legal foundation across multiple functional areas. What you&aposll do Assist in drafting, reviewing & organizing contracts (NDAs, MoUs, vendor & client agreements) Support legal aspects of HR, operations, finance, and compliance Conduct legal research on topics like IPR, employment law, global regulatory frameworks, privacy Help shape internal policies, processes, and risk management Track key changes in law relevant to our product & ...

About Company Founded in 2011, ReNew, is one of the largest renewable energy companies globally, with a leadership position in India. Listed on Nasdaq under the ticker RNW, ReNew develops, builds, owns, and operates utility-scale wind energy projects, utility-scale solar energy projects, utility-scale firm power projects, and distributed solar energy projects. In addition to being a major independent power producer in India, ReNew is evolving to become an end-to-end decarbonization partner providing solutions in a just and inclusive manner in the areas of clean energy, green hydrogen, value-added energy offerings through digitalisation, storage, and carbon markets that increasingly are integ...

Responsibilities : Prompts and support for compliance with government funding (Callaghan Innovation) reporting requirements. Prompts and support to achieve compliance for BCM financial reporting. Maintenance, amendment and facilitation of signatures for legal templates, including Confidentiality Agreements, Memorandum of Understandings, Term Sheets Founder professional development admin coordinate online training courses and invite founders. Information management support for tracking disclosures, decisions, research and connections. Funding grants submission and close out support What youd gain: red: Invaluable hands-on experience working alongside seasoned developers. Opportunity to learn ...

Jubilant Pharma Limited is a global integrated pharmaceutical company that offers a wide range of products and services to customers across different 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. JGL operates two manufacturing facilities in Mysore, Karnataka,...

As a Quality Control (QC) Analyst at Jubilant Generics, you will be responsible for various tasks related to ensuring the quality and compliance of pharmaceutical products. Your role will involve sampling and analyzing packing materials and raw materials, conducting in-process quality control, and preparing specifications and test procedures. Additionally, you will be responsible for maintaining artwork and shade cards, as well as calibrating and validating instruments and equipment. Your attention to detail will be crucial in recording analytical data accurately and preparing records of analysis for both raw materials and finished products, including stability samples. In this role, it is e...

As a Company Secretary, you will play a vital role in ensuring adherence to legal and regulatory requirements, maintaining company records, and assisting in board and shareholder meetings. Your attention to detail and knowledge of corporate laws will help us maintain transparency and uphold the highest standards of corporate governance. Responsibilities: Compliance Management: Ensure compliance with applicable laws, regulations, and guidelines. Stay updated on changes in corporate governance practices and maintain a strong understanding of legal and regulatory requirements. Corporate Governance: Assist in establishing and maintaining effective corporate governance practices. Coordinate board...

Extremely Strong and Competent Professional for Patent Drafting andOpposition/Revocation Matters with a minimum 5 years of PQE. Ability to deeply understand technical subject matters. Should have a strong understanding of Patent laws. Fast learning capabilities along with the ability to work independently aremust. Should have clarity in verbal communications so as to efficiently discuss withclients, and manage client projects, mandates, business developmentmandates, and client relationships. Should be a strong team player and willing to take additional responsibilities pertaining to trainings, speaking opportunities, client communications,overseeing docketing team to ensure smooth client int...

Extremely Strong and Competent Professional for Patent Drafting and Opposition/Revocation Matters with a minimum 5 years of PQE. Ability to deeply understand technical subject matters. Should have a strong understanding of Patent laws. Fast learning capabilities along with the ability to work independently aremust. Should have clarity in verbal communications so as to efficiently discuss withclients, and manage client projects, mandates, business developmentmandates, and client relationships. Should be a strong team player and willing to take additional responsibilities pertaining to trainings, speaking opportunities, client communications, overseeing docketing team to ensure smooth client i...

SAP GTS Number of Openings 1 (JL 5) ECMS ID in sourcing stage Assignment Duration 6 months Total Yrs. of Experience 7+ Relevant Yrs. of experience 7+ Detailed JD (Roles and Responsibilities) Responsibilities: 1. Collaborate with cross-functional teams to ensure seamless integration between SAP GTS and other SAP modules (e. g. , SD, MM) and third-party middleware platforms. 2. Manage stakeholder expectations and provide strategic guidance on trade compliance processes 3. Design, implement, and support SAP GTS module aligned with business needs. Skillset: Relevant professional IT experience in the related functional area Consistent record of broad industry experience and solid understanding of...

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 ...

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 ...

* Process development, scale up and technology transfer of products from R&D to Pilot plant upto commercial batches to production department as per regulatory requirement * Day to day lab experiment planning & to ensure execution Required Candidate profile * To ensure requirement of raw materials as per experiment planned in R&D and pilot plant. *Complete literature search with IPR status study, ROS finalization, lab experiment planning.

" 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 Roor...

Responsibilities: * Business development in intellectual property domain: patent searches, patent illustrations, patent drafting, trademarks, copyrights. * Lead generation and conversion. * Client management and relations. * Team coordination

The role involves managing a comprehensive support initiative designed for startup life cycle management at iCreate ensuring a smooth transition of selecting onboarding monitoring managing as per the program. Key Responsibilities: Startup Coordination: Facilitate connectivity between mentors and startups to ensure a valuable matrix of guidance and insights. Performance Monitoring: Regularly evaluate program effectiveness based on predefined metrics and participant feedback. Reporting and Compliance: Maintain comprehensive records of specific programs, incubation activities, and outcomes as defined. Teamwork: Work closely with different internal and external stakeholders of the program. Commu...

As a global integrated pharmaceutical company, Jubilant Pharma Limited offers a diverse range of products and services to customers worldwide. The business is structured into two main segments: Specialty Pharmaceuticals and Generics & APIs. Jubilant Generics (JGL), a subsidiary of Jubilant Pharma, has Research & Development units in Noida and Mysore, India, along with manufacturing facilities in Mysore, Karnataka, and Roorkee, Uttarakhand. The Mysore facility, spread across 69 acres, is a USFDA approved site primarily focused on manufacturing APIs for Lifestyle driven Therapeutic Areas such as CVS and CNS. The Roorkee facility is a state-of-the-art site approved by multiple regulatory bodies...