212 Patents Jobs - Page 5

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.,

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

As a Senior ML/AI Engineer at our Technology Innovation Lab, you will be a key member of a cross-disciplinary team dedicated to advancing AI and intelligent automation at HERE. Your primary responsibility will be to develop cutting-edge machine learning systems that leverage Agentic AI, Generative AI, and foundational ML techniques to drive the next generation of applications. Collaborating closely with technical leads, researchers, and engineers, you will prototype solutions to address real-world spatial, operational, and knowledge-driven challenges. Your role will involve architecting and implementing AI-first systems using technologies such as Large Language Models (LLMs), Autonomous Multi-Agent Architectures, and Classical ML models like regression, clustering, XGBoost, SVM, and tree-based learners. Leading the development of Agentic AI solutions will be a core aspect of your role, encompassing tasks such as orchestration, memory/context management, tool invocation, and human-agent collaboration. You will also be responsible for designing and delivering end-to-end Generative AI applications for various purposes including text generation, summarization, code synthesis, image generation, and multi-modal interfaces. Your expertise in deep learning techniques, including CNNs, RNNs (LSTM, GRU), GANs, Diffusion Models, Transformers, and Graph Neural Networks, will be crucial for tackling real-world tasks in vision, language, and planning. You will collaborate across teams to translate domain-specific problems into scalable, explainable, and production-ready AI solutions while incorporating responsible AI principles. Staying at the forefront of AI research will be essential, as you evaluate and implement emerging LLM models, agentic frameworks, and open-source innovations to ensure technical currency in this rapidly evolving field. You will also design and lead experiments across advanced AI/ML areas, encompassing computer vision, NLP, LLMs, and emerging domains like quantum computing, distributed computing, 3D modeling, AR/VR, and LiDAR/drone data processing. Writing efficient, production-quality code using Python and leveraging frameworks like PyTorch, TensorFlow, and Spark for large-scale ML training and inference will be part of your daily tasks. Defining and tracking KPIs at both individual and business unit levels, in collaboration with your manager, will ensure that your work drives impactful innovation. Supporting and mentoring engineers and data scientists in best practices related to prompt design, agent workflows, evaluation frameworks, and research translation will also be part of your responsibilities. Additionally, contributing to HERE's innovation footprint through patents, internal IP development, and peer-reviewed publications will be encouraged. To qualify for this role, you should hold a Master's degree or Ph.D. in Computer Science, AI/ML, Mathematics, or a related field. Candidates with a Master's degree should have 5-7 years of experience, while Ph.D. holders may have 3-5 years of relevant experience. A strong understanding of ML fundamentals, hands-on experience with deep learning architectures, proficiency in Python, and familiarity with ML frameworks are essential qualifications. Curiosity and exposure to adjacent technologies like TinyML, Quantum Computing, or 3D modeling/AR will be considered advantageous. At HERE Technologies, we are a location data and technology platform company dedicated to empowering our customers and making a positive impact on people's lives. If you are passionate about driving innovation and creating positive change in an open world, we invite you to join us on this exciting journey.,

- Exp in Machine Learning / AI / NLP / LLM - Strong track record of applied research supported by publications, blog articles etc. - Hands on exp to build and deploy ML models in production on prem or using cloud services

SENIOR QUALITY CONTROL ANALYST Job Objective: The Quality Control (QC) Analyst specializing in Method Validation and Method Development is responsible for developing, validating, and transferring analytical methods for pharmaceutical raw materials, intermediates, and finished products. The role ensures compliance with regulatory requirements and contributes to continuous improvements in analytical methodologies. Qualifications: Bachelors/Masters degree in Pharmaceutical Sciences, Chemistry, Analytical Chemistry, or related field. Experience: More than 8 years of experience in method validation, method transfer, and regulatory compliance within a pharmaceutical QC or analytical development environment. Job Responsibilities: Method Development & Optimization: Develop and optimize analytical methods for assay, dissolution, related substances, and residual solvents using techniques like HPLC, GC, UV-Vis, FTIR. Establish and refine chromatographic conditions, mobile phases, and detection parameters for improved sensitivity and reproducibility. Conduct forced degradation and stability-indicating method development as per ICH Q1A guidelines. Method Validation & Transfer: Perform method validation as per ICH guidelines covering accuracy, precision, specificity, linearity, robustness, and system suitability. Prepare and review method validation protocols and reports. Execute method transfer activities between R&D, QC, and manufacturing sites following GMP requirements. Regulatory Compliance & Documentation: Ensure analytical methods meet US FDA, EU GMP, MHRA, WHO, and other regulatory expectations. Maintain accurate documentation as per Good Documentation Practices (GDP). Support regulatory filings by preparing analytical method validation reports and technical dossiers. Assist in responding to regulatory queries and audits related to analytical methods. Instrumentation & Troubleshooting: Operate and maintain analytical instruments such as HPLC, GC, UV-Vis, FTIR, and dissolution testers. Troubleshoot chromatographic issues related to retention time shifts, peak tailing, and resolution problems. Participate in instrument qualification (IQ/OQ/PQ) as needed. Collaboration & Process Improvement: Work closely with R&D, Manufacturing, and Quality Assurance teams for seamless method transfer. Investigate out-of-specification (OOS) and out-of-trend (OOT) results to identify root causes. Contribute to continuous improvements in analytical techniques and laboratory efficiency. Technical Skills: Strong expertise in HPLC, GC, UV-Vis, FTIR

Key Skills: AI/ML Research, Algorithm Design, Neural Architectures, Data Analysis, AI/ML Libraries, Natural Language Processing, Computer Vision, Multi-modal Data Analytics, Research Publications, Patents, Academic Collaboration, Communication Skills, Scientific Leadership Roles & Responsibilities: Identify and frame new research projects by brainstorming with other researchers to scope critical research challenges and develop innovative solutions. Design new algorithms, neural architectures, and computing methodologies through theoretical and experimental research. Conduct rigorous data analysis to support proposed solutions and demonstrate their practical applications. Share key findings with internal leadership, including Project Leaders, Research Managers, and Project Directors. Draft and submit patents, and author research papers for prestigious AI/ML/CV/NLP conferences and journals. Engage with academic institutions and collaborators to expand 's network and promote cutting-edge AI research. Collaborate with applied researchers to transform core scientific discoveries into practical solutions. Facilitate the transfer of research outcomes to business units and external clients, driving real-world impact. Lead scientific projects towards impactful breakthroughs. Translate complex research into understandable and actionable insights through exceptional communication, report writing, and presentation skills. Willingness to learn new fields, explore uncharted territories in AI, and develop cross-disciplinary skill sets. Experience Requirement: 4-7 years of research experience post-PhD in AI, Machine Learning, Computer Science, or a related field. Advanced expertise in AI/ML, with a deep understanding of machine learning, statistical theory of learning, and AI concepts and their practical application in domains like natural language, computer vision, and multi-modal data analytics. Proven track record of publishing in top-tier AI/ML conferences such as ICML, ICLR, NeurIPS, AAAI, IJCAI, AISTATS, SIGKDD, ACL, NAACL, CVPR, ICCV, ECCV, etc. Strong programming skills in AI/ML with hands-on experience in major AI platforms and tools. Experience in deploying AI frameworks like AI agents and autonomous systems is desirable. Education: B.Tech M.Tech (Dual), B.E., B.Tech, M.E.

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.

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

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.,

As an Assistant Professor in the Department of Computer Science and Engineering (CSE) or Artificial Intelligence and Data Science (AIDS) at Kathir College of Engineering in Coimbatore, Tamil Nadu, India, you will be required to have an M.Tech/M.E degree in Computer Science, Computer and Communication, AI, or Information Technology. Freshers with a postgraduate degree are welcome to apply, but candidates pursuing or holding a Ph.D. are preferred. Your role will involve utilizing your excellent communication and strategic communication skills, along with experience in curriculum development and research within your respective field. University teaching experience is necessary, as well as the ability to work effectively as part of a team. Strong problem-solving and analytical skills are essential, along with a Ph.D. completed or in progress in your respective field and a track record of published research papers, journals, or patents. Kathir College of Engineering, founded in 2008, is an autonomous institution dedicated to offering quality education and promoting research and innovation. The college provides undergraduate and postgraduate programs in various engineering and technology fields, supported by experienced faculty, well-equipped laboratories, a vast library, and modern infrastructure. This full-time on-site role offers a salary in accordance with AICTE norms. As an Assistant Professor, you will be responsible for teaching undergraduate and postgraduate courses, developing curriculum, conducting research, and contributing to the strategic communication efforts of the Department of Electronics and Communication Engineering.,

Patent Portfolio Management Patentability Assessment Patent Drafting & Filing (India and International) Patent Prosecution & Examination Response Handling Patent Landscape and Infringement Analysis Freedom to Operate (FTO) Analysis IP Enforcement Strategy & Infringement Notice Preparation Knowledge of Patent Laws (India, US) IPR Documentation: Counterclaims, Written Statements, Evidences Expertise in Patent Search Databases (e.g., Derwent, Patsnap, Orbit, etc.) Technical Patent Search: API, NCE, NDDS, Formulation, Technology

Responsibilities: * Lead business growth through strategic planning and execution. * Manage sales pipeline from lead generation to close. * Collaborate with engineering team on IP development. Health insurance

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.,

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to customers across geographies. The business is structured into two segments: Specialty Pharmaceuticals and Generics & APIs. Specialty Pharmaceuticals includes Radiopharmaceuticals, Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products. Generics & APIs includes 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 manufacturing facilities in Mysore, Karnataka, and Roorkee, Uttarakhand, engaged in APIs and Dosage manufacturing, respectively. The Mysore manufacturing site, spread over 69 acres, is USFDA approved and focuses on Lifestyle driven Therapeutic Areas like CVS and CNS. It is a market leader in four APIs and among the top three players for three others. The Roorkee facility is state-of-the-art, approved by multiple regulatory bodies, and works on a B2B model for EU, Canada, and emerging markets. Both manufacturing units are supported by around 500 research and development professionals based at Noida and Mysore. The R&D focuses on developing new products in API, Solid Dosage Formulations, Sterile Injectable, Semi-Solids, Ointments, Creams, and Liquids. All BA/BE studies are conducted in-house at an 80 Bed facility with global regulatory accreditations. JGL's Regulatory Affairs & IPR professionals ensure a unique portfolio of patents and product filings in regulatory and non-regulatory markets. The revenue of Jubilant Pharma has been increasing, with INR 53,240 Million in the Financial Year 2018 -19 compared to INR 39,950 Million in 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 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, has Research & Development units in Noida and Mysore, India. JGL operates two manufacturing facilities in Mysore, Karnataka, and Roorkee, Uttarakhand, specializing in APIs and Dosage manufacturing. The Mysore manufacturing location, spread over 69 acres, is a USFDA approved site focusing on Lifestyle driven Therapeutic Areas such as CVS and CNS. It is a market leader in four APIs and amongst the top three players for three others. The Roorkee facility is a state-of-the-art site approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO, and Brazil ANVISA, following a B2B model for EU, Canada, and emerging markets. Both manufacturing units are supported by around 500 research and development professionals based in 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. In-house BA/BE studies are conducted at an 80 Bed facility with multiple global regulatory accreditations. JGL's Regulatory Affairs & IPR professionals maintain a unique portfolio of patents and product filings in regulatory and non-regulatory markets. The revenue of Jubilant Pharma has been on a consistent rise, reaching INR 53,240 Million during the Financial Year 2018-19 compared to INR 39,950 Million in 2017-18. For more information about the organization, please visit www.jubilantpharma.com.,

Hi, We are having an opening for Senior Executive IP (prosecution) at our Mumbai/ Baroda location. Job Summary : Management of the branded portfolio from IP perspective Areas Of Responsibility : Life Cycle management of branded portfolio from IP perspective including competition tracking Preparation of landscape and infringement analysis Identifying and tracking competition Patentability evaluation, patent filing and prosecution Preparation for enforcement of IP Search and analysis- in API, NCE, formulation, technology, Devices related Inventions IP due diligence for technologies and products for in-licensing IP support for out-licensing projects Freedom to operate for in-house branded portfolio Performing validity analysis of blocking patents Identifying new opportunities for in-licensing Educational Qualification : M.Pharm /Ph.D in Pharmacy Specific Certification : Certification on patent law- preferred Skill (Functional & Behavioural): Patent drafting and Prosecution Experience : 5 to 7 years

As a Legal Lead based in Mumbai, you will be responsible for reviewing and drafting various software business contracts, which include RFPs, tender documents, Pos, MSAs, Service Agreements, and Vendor Agreements. You will also be involved in contract negotiations with internal teams, customers, vendors, and service providers. Ensuring contractual and regulatory compliance will be a key aspect of your role. Your expertise in Intellectual Property Rights (IPR) related to Trademarks, Copyrights, Patents, and Domain Names will be essential. You will be driving the contract lifecycle from drafting to completion of the negotiation process and contract execution. Knowledge of Data Protection Laws, GDPR, and Cyber laws will be advantageous. Maintaining the Contracts Repository and conducting legal research by reviewing case laws, Acts, Rules, Notifications, etc., will be part of your responsibilities. You should have excellent drafting, negotiation, and communication skills. Experience with Contract management systems and defining the Contract lifecycle process will be beneficial. To qualify for this position, you must have completed LL.B / LLM from reputed Universities/Institutions and possess 4 - 6 years of relevant non-litigation experience. Strong communication skills, global exposure, and corporate experience are required. If you meet the qualifications and are available to join within 15 days, we encourage you to send your resume to sayanti.roy1@learningmate.com.,

Join a growing, dynamic, and innovative team that has established itself as the market leader in Intellectual Property management solutions. ANAQUA provides Intellectual Asset. Management Software and Services to help companies and law firms improve the management of their IP portfolios to gain a competitive advantage. With a combination of adaptive software, great people, and a proven implementation methodology, Anaqua partners with its clients to build global capabilities that integrate workflows and web-based collaboration across the IP lifecycle and is committed to 100% client satisfaction. Position Overview: Anaqua is looking for a highly motivated and proactive Docketing expert with Patent knowledge who is eager to help us to attain our continuing growth goals. Youll Love This Job if You Like To: • Ensuring correct Patent Docketing & De-Docketing of deadlines in IPMS along with uploading & linking of relevant documents in the respective matter • Ensuring correct bibliographic information is updated, generating correct reminders so that the paralegals/attorneys are informed timely of the actions due • Identify key information in the client-provided instructions and verify/audit it in the IPMS correctly, as per the clients instructions • Review patent prosecution-related documents (US & Non-US) received via shared mailbox as per the standard operating procedures (SOP) • Perform Quality Audits on the allocated documents as per client requirements within the allocated time • Responsible for all aspects of Patent internal quality audit for US and Non-US Jurisdictions • Report and describe docketing-related queries to the manager or client (if needed) • Assist in training and ramp up of new joiners • Ensuring the correct internal process is followed and reporting in case of any deviation observed Skills and Experience Required: • Minimum 2 years of experience in the related role • Knowledge of filing and prosecution practices in the USPTO, PCT and other major jurisdictions • Prior experience of working on Anaqua/Pattsy Wave platform would be an added advantage • Ability to prioritize and multi-task to perform role smoothly without missing deadlines • Good written and verbal communication skills (English) • Law graduates with relevant experience will be preferred

Roles & Responsibilities: Conduct novelty/patentability, invalidity, and landscape searches Prepare and file patent applications with support from external counsels Draft responses to office actions and support prosecution activities for patents, designs, and trademarks Interact with inventors and R&D teams to extract technical details and develop invention disclosures Support Freedom to Operate (FTO) analysis and competitive IP intelligence study Manage deadlines for filings, renewals, and prosecution timelines Maintain and update internal IP databases and records Provide support in IP due diligence, risk assessment, and litigation assistance as required. Preferred candidate profile Work Location : Bangalore Education: B.E/B. Tech in Mechanical, Electrical & Electronics, Automotive Domain Experience: 6 - 8 Years of Relevant Experience in an IP Law Firm or In-House IP Team Preferred: Registered Indian Patent Agent Any Certification in IP or Innovation Understanding of IP laws and filing procedures (Indian, PCT, Madrid, Hague System) Exposure to IP tools such as Derwent, PatSnap, Orbit, or similar As an IP Engineer, you will play a key role in supporting the companys intellectual property strategy. You will be involved in conducting patent searches, drafting patent applications, assisting with prosecution, and coordinating with inventors and legal teams to protect innovative ideas and technologies.

Roles & Responsibilities: Conduct novelty/patentability, invalidity, and landscape searches Prepare and file patent applications with support from external counsels Draft responses to office actions and support prosecution activities for patents, designs, and trademarks Interact with inventors and R&D teams to extract technical details and develop invention disclosures Support Freedom to Operate (FTO) analysis and competitive IP intelligence study Manage deadlines for filings, renewals, and prosecution timelines Maintain and update internal IP databases and records Provide support in IP due diligence, risk assessment, and litigation assistance as required. Preferred candidate profile Work Location : Bangalore Education: B.E/B. Tech in Mechanical, Electrical & Electronics, Automotive Domain Experience: 6 - 8 Years of Relevant Experience in an IP Law Firm or In-House IP Team Preferred: Registered Indian Patent Agent Any Certification in IP or Innovation Understanding of IP laws and filing procedures (Indian, PCT, Madrid, Hague System) Exposure to IP tools such as Derwent, PatSnap, Orbit, or similar As an IP Engineer, you will play a key role in supporting the companys intellectual property strategy. You will be involved in conducting patent searches, drafting patent applications, assisting with prosecution, and coordinating with inventors and legal teams to protect innovative ideas and technologies.

SagaciousElevate is looking candidates for Senior Patent Analyst role for Gurugram location. Job Requirement: Skills: Patentability, Invalidity, FTO, Landscape Education: B.E/B.Tech/M.E/M.Tech (Electrical, Electronics, Electronics & Telecommunications, Instrumentation); B.E/B.Tech/M.E/M.Tech/B.Sc/M.Sc(Biochemistry or Biotechnology) Job Location: Gurugram Experience: 2-6 Years Interested candidates can share their updated CV on suchi.rahangdale@elevate.law

Lead and manage the legal department across multiple jurisdictions, including the US, India, the EU, and China. Strategic IP Management is Crucial with several other factors

Job Role: Business Development Executive – Intellectual Property Rights Company: Law firm Qualification: Any Graduate/MBA Experience: Min.1year Salary: upto 40k Location: Banjarahills Interested contact 8247381453 share CV laxmi@hireiton.com Required Candidate profile Qualification: Any Graduate/MBA Experience: Min. 1years Skills: Strong understanding of intellectual property concepts (trademarks, patents, copyrights, designs) communication and presentation skills

Greetings from Kashiv Biosciences !!! We are looking for an experienced IP professional with 4-8 years of dedicated experience in patent drafting, prosecution, and analytics in the biotechnology. The ideal candidate should have a strong life science background.(Biotechnology/Microbiology/Biochemistry) and a proven track record of working on patent applications related to biologics, biosimilars, or pharmaceutical technologies . This role will focus on managing patent drafting, global prosecution, freedom-to-operate (FTO) analyses, and supporting IP strategy across the biosimilar pipeline. Key Responsibilities: Patent Drafting & Prosecution: Independently draft and review patent specifications, claims, and responses to office actions (US, EP, IN, and other major jurisdictions). Coordinate with inventors, R&D scientists, and external counsel for t echnical data collection and application filings . Manage timelines and filings for patent applications and ensure procedural compliance. Patent Analytics: Conduct prior art searches, invalidity and opposition searches using databases such as Derwent, Orbit, PatSnap, and Google Patents . Perform patentability assessments, competitive intelligence, and white-space analysis. Freedom-to-Operate (FTO): Perform FTO analysis to identify third-party risks and provide mitigation strategies. Assist in developing IP risk profiles and clearance strategies for biosimilar programs. Portfolio & Docket Management: Maintain and update internal IP records, invention disclosures, and portfolio tracking sheets. Support IP audits and manage annuity tracking in collaboration with the legal and compliance teams. Cross-Functional Collaboration: Liaise with scientific, regulatory, and legal teams to align IP activities with project goals. Summarize complex IP and technical issues clearly for stakeholders across functions. Candidate Details: The Candidate should possess Masters degree in Biotechnology, Microbiology, Biochemistry, or a related life science field. The candidate should have 4-6 years of hands-on experience in patent drafting, prosecution, and analysis preferably i n-house or with a reputed IP law firm . Solid understanding of global patent laws (especially Indian, US, and EP patent practices). Strong scientific and analytical skills with attention to detail. Excellent communication and documentation skills. The candidate should have Passed Indian Patent Agent Examination. The candidate should have Experience with BPCIA framework, EPO opposition, or Indian pre-grant/post-grant opposition. Familiarity with SPCs, PTEs, and exclusivity timelines. Interested candidates please share the resume at manan.hathi@kashivindia.com