70 Patent Search Jobs - Page 3

Patent Analyst Polymer Science/Polymer Engineering Position Summary: The Patent Analyst will be responsible for conducting thorough patent searches, analyzing patent landscapes, and providing detailed technical insights related to Polymer innovations The ideal candidate will have a strong technical background in Polymer Science, combined with excellent analytical and research skills, Key Responsibilities: Patent Search and Analysis: ? Conduct comprehensive patent searches using various databases and tools, ? Analyze patent documents to identify relevant patents and assess their impact on current and future projects, ? Prepare detailed reports summarizing findings and providing strategic insights, Patent Landscape Analysis: ? Create and maintain patent landscapes to identify trends, white spaces, and potential opportunities, ? Monitor competitors' patent activities and provide competitive intelligence, ? Assist in drafting and reviewing patent applications, ensuring technical accuracy and completeness, Qualifications: ? Bachelor's Degree in Polymer Science/Polymer Engineering ? Master's degree in Polymer Science/Polymer Engineering ? 1 to 3 years of experience in patent analysis, preferably within the Polymer Science/Engineering sector, ? Strong understanding of patent laws, procedures, and databases (e-g , USPTO, EPO, WIPO), ? Excellent research and analytical skills, with attention to detail, ? Proficiency in using patent search tools and databases, ? Strong written and verbal communication skills, ? Ability to work independently and collaboratively in a team environment,

We are seeking a Senior Specialist, Intellectual Property for our North America Group (NAG). The incumbent will be based in India, and report to the Lead, Intellectual Property Counsel - North America. As a Senior Specialist in the IP department, you will collaborate with US Counsel and internal stakeholders to design and implement IP strategies to advance Dr. Reddy’s interest in providing affordable health care solutions. Roles & Responsibilities Work with US Counsel in managing ANDA, 505(b)(2), BPCIA, and PM(NOC) patent litigations, including post-grant patent office proceedings by developing and implementing claims and defenses. Assist in discovery, witness preparations, and competitive landscape analysis. Identify strategies related to Paragraph IV certifications and Section viii carve-outs. Work with US Counsel and DRL R&D in securing freedom-to-operate for Dr. Reddy’s products, including clearance of Orange Book and unlisted patents for the bulk API, route of synthesis, finished dosage form and polymorphs. Conduct prior art, patentability, landscape and freedom-to-operate searches. Examine patents, file histories, prior art, ongoing litigations, and citizen’s petitions for possible Paragraph IV and related strategies for ANDA and 505(b)(2) products. Develop and provide IP inputs as part of product selection. Provide IP prosecution strategy, including by collaborating with R&D on innovation and drafting patent applications. Conduct IP due diligence and provide IP support towards business development activities. Qualification Educational qualification: Advanced Degree in pharmaceutics, pharmacology, pharmaceutical chemistry, or similar discipline required (MS or PhD); LLB preferred. Minimum work Experience: 14+ years of experience working with life science, biotechnology, and/or pharmaceutical companies in Intellectual Property is required, wherein 6+ years were spent assisting on complex intellectual property issues for the United States litigations. Skills & attributes: Technical Skills Experience in Intellectual Property (IP) domain Experience developing strategies for and assisting in the management of ANDA litigations in the US Skilled in infringement/invalidity analysis, freedom to operate, filing and prosecution, Market launch analysis. Experience leading product Identification and selection in perspective of complex Injectable, inhalation, OSDs in different geographies. Sound knowledge of technologies used in various dosage forms. Due diligence experience for North America region. Experience with both small molecules and biologics, not required, but preferred Behavioural Skills Excellent communication and interpersonal skills. Strong analytical and problem-solving abilities. Good Negotiation and Influencing skills. Ability to work collaboratively with Regulatory and cross-functional teams across US - India time zones. People management skills Additional Information Benefits Offered At Dr. Reddy’s we actively help to catalyze your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Role: Contractual We are seeking a contract-based employee for a duration of 3 months. 3-5 years of experience in patent analysis, IP strategy, or patent portfolio management. • Hands-on experience with patent databases, with strong proficiency in Orbit and/or Derwent Innovation. Strong grasp of patent law, claim interpretation, and international filing practices (USPTO, EPO, CNIPA, etc.). Excellent written and verbal communication skills with the ability to present complex findings clearly. Experience working with multidisciplinary teams across legal, technical, and business functions. Responsibilities : Lead and execute in-depth patentability, freedom-to-operate (FTO), and infringement analyses across multiple jurisdictions. Perform landscape and white-space analyses to guide R&D investments and product development. Analyze competitor IP portfolios, patent trends, and emerging technologies to inform strategic decisions. Mentor junior analysts and contribute to the development of best practices in patent research and documentation. Present IP insights and strategy recommendations to stakeholders, including leadership, legal, and product teams. Maintain current knowledge of international patent laws, classification systems, and relevant industry standards. Preferred candidate profile : Bachelors or Masters degree in a technical field . We are seeking a contract-based employee for a duration of 3 months.

The Intellectual Property Search Analyst will be responsible for performing prior-art searches and evaluating third-party patent rights with IP Managers. Main Responsibilities & Tasks: Perform prior-art searches for patentability, FTO and invalidity studies in external and internal patent databases Facilitate patent mapping and patent landscaping in cooperation with IP Managers, Product Development and Corporate Research to explore emerging technologies and to identify future IP trends Evaluate 3rd-party patent rights in close cooperation with IP Managers and Product Development and Corporate Research colleagues Evaluate new IP search and analysis tools and test their performance (benchmarking) in comparison with IP tools already in use at Sartorius Qualification & Skills: Master degree in biochemistry, biotechnology, life sciences, biology, chemistry, data analytics or engineering Qualification as an patent or IP search specialist would be an asset Minimum 3 years of professional experience as an IP search expert for a multinational corporation or commercial IP search service provider Expertise in designing and implementing IP search strategies in Derwent Innovation, Total Patents, PatSnap, STN, Questel or other commercially available patent search tools Robust understanding of the basics of patent laws with regard to patentability, FTO analyses, invalidity procedures Excellent analytical skills, attention to detail, excellent interdisciplinary communication skills, intercultural competence for working in a multinational team Team player, ultrafast learner, personal resilience, perseverance, quick understanding of complex technical problems, meticulousness Fluent in English About Sartorius Sartorius is part of the solution in the fight against cancer, dementia, and many other diseases. Our technologies help translate scientific discoveries into real-world medicine faster, so that new therapeutics can reach patients worldwide. We look for ambitious team players and creative minds, who want to contribute to this goal and advance their careers in a dynamic global environment. Join our global team and become part of the solution. We are looking forward to receiving your application. www.sartorius.com/careers

We are looking for a Patent Search Analyst to join our IP Search Team in Noida for fixed term. This is a great opportunity to work with Fortune 100 clients to support them on various phases in IP Life cycle management. The team member will work on various projects such as Prior-art Searching (Patentability / Validity / Invalidity) , Evidence-of-Use, Freedom-to-Operate searches etc. in chem/Pharma domain. We would love to speak with you if you have skills in any of the above-mentioned services and/or have the aptitude to work on emerging technologies. About You - experience, education, skills, and accomplishments Bachelor s Degree or equivalent in Life Sciences, Biotechnology or related domain 5 Years of IP service experience intermediate knowledge of US, European, and/or other jurisdiction patent law Expert in utilizing patent and non-patent literature search databases Proficient in working with MS Word MS Excel It would be great if you also have - M. Sc/ M. Tech/Ph. D degree in Life Sciences, Biotechnology or related domain Proficiency in Microsoft Excel, including chart/graph generation, and data handling. What will you be doing in this role Execute searches of low, medium, and high complexity for technical information to support our customers in making patent related decisions including patentability (novelty), State of the Art (SoA), Freedom-to-Operate, (In)validity, and Patent Analytics services. Perform qualitative analysis of patents and non-patent literature from a technical perspective. Quickly understand and discern the technical nuances of a patent or non-patent literature disclosure and what may distinguish it from the prior art. Ensure that a thorough search of the prior art is performed based on project scope and the most relevant prior art is identified through demonstration of a complete search strategy. Contribute to customer satisfaction through construction of high-quality deliverables that are self-reviewed, striving for first time right. Communicate and collaborate with customers on individual projects and ensure their expectations and requirements are met. Meet internal deadlines with deliverables that meet project objectives and customer expectations. Build IP patent and non-patent literature database knowledge and skills by participating in trainings and knowledge sharing sessions. Proactively update technical skill set and hands-on subject matter expertise in the technologies that are being deployed and/or used widely in industry. Contribute towards achieving team Key performance Indicators (KPIs). Participate in continuous improvement initiatives to drive measured improvements in processes and deliverables through the CI framework. Ensure all own Project Insight tasks are completed in an accurate and timely manner. Adherence to organizational policies and procedures. Hours of Work This is a full-time role requiring 40 working hours per week based out of Noida, India (IST). Work Mode-Hybrid

Experience from major pharma industries in Non-oral Products: Topical product and transdermal product. Experience in end-to-end topical product development activities for generic product development ANDA (Cream, ointment, gel, solution, lotion, foam, patch etc.) as well as NDA 505(b)(2), 505(b)(1). Experience in execution of lab scale manufacturing, reverse engineering, analytical know-how, plant level manufacturing activities; scale-up and exhibit batches based on quality principles QbD, QTPP, CQA, CMA, CPP, RA, FMEA. Experienced scientist to perform experiments for development of optimum prototypes (generic, non-infringing composition and robust manufacturing process) with diverse class of drugs & prodrugs (sensitive to pH, acid, base, temperature, oxygen, humidity). Experience in regulatory documentation CMC, MF, BMR, PDR, controlled correspondence for CMC, Biowaiver & Dossier preparation for US-FDA, EU-EMA, AU-TGA & DCGI through successful filing. Experience in working with cross-functional teams (ADD, MSTG, production, QC, QA, RA, IPC, PMO, BD, Microbiology, Pharmacology etc.) to achieve project goals - Filings and subsequent approvals. Knowledge and develop continuous understanding on competitive intelligence, due diligence, US-FDA quality concepts, statistics and global pharma trend analysis to support new product evaluation & introduction. Job Responsibilities: To design, conduct and verify/review experiments to develop a robust formulation . To do literature search, patent search, prepare summary report and review. To prepare product development reports and protocols. To do product scale-up, exhibit batches and prepare reports for product filing and regulatory queries including post filling and post approval market queries. To prepare documents (i.e. PDR, CPD etc.) for regulatory submission Group work co-ordination. Project status report preparation. Experimental result review, interpretation and conclusion. To prepare technology transfer documents. To procure raw materials (API / excipients), packaging materials, innovator samples in consultation with packaging/purchase department. To do product validation, site transfer/change activities of products. To write Laboratory Notebook to enter details related to drug product manufacturing. To prepare test request for analysis of raw materials (API/Excipients) and Drug product.

Support matters involving patent related information, mining, collation, analysis and transformation of complimentary pieces of information. You are expected to work collaboratively with engineering and attorneys in researching, analyzing and presenting key observations using analytics and presentation tools. You are expected to work on freedom to market, validity and landscape projects with a high level of diligence. You will apply significant product and technology knowledge of aligned business domain, and use the same to draft and prosecute patent applications. Key Responsibilities Design project scope (SOW) Deliver targets W.R.T quality Search and classify practices US, EP, India patent process Prosecute and draft portfolio Connect with customers Patent applications Product/technology knowledge Mining, collation, analysis WE VALUE Juggle many priorities and competing demands Some professional experience consisting of research, development and engineering (RDE) Some hands-on experience on IP matters like patent search, analytics, prosecution, drafting, patent portfolio management Connect information to transform into enabling insights Clear and thoughtful communication skills Interpersonal skills and ability to handle pressure Accurately identify a variety of problems and issues Influence and collaborate effectively with diverse audience Exceptional written, oral and presentation skills

Job Location: Bangalore We are looking for Patent Analyst to join our team in Bangalore Job Description: Hands-on experience in technology landscapes, patentability, freedom to operate, invalidity search, and infringement reports Strong knowledge of Intellectual Property & Patent Law Familiarity with patent databases and tools Detail report summarization of patent search and analysis Analytical skills to analyze and interpret the invention disclosure on its novelty Conduct patent and non-patent literature searches Desired Candidate Profile: Immediate joiners located in Bangalore or willing to relocate preferred Excellent communication skills Qualification: Electronics, Electrical, Mechanical, Telecommunication, Computer Science, or any engineering discipline with expertise in the mentioned IP skills Work experience: 1-2yrs

1. Lead patent search projects, conduct FTO, patentability, and portfolio analyses. 2. Utilize technical expertise in ECE, Mechanical, or CS domains. 3. Manage team, engage in technology scouting, and deliver strategic IP insights.

Coordinate with internal (i.e. Execution team, API-RA, Plant, SCM, CPPK etc.) as well as external counterparts (i.e. external API manufacturing and testing sites etc.) Trigger request for all the administrative documents like foreign CPP, Indian CoPP/FSC/WHO GMP from respective CFT's and list down the open issues, also provide the document request to plant. To co-ordinate and understand the on-going review status of the product in the lead markets and update the API Plus project simultaneously demanding its review stage and tentative approval timeline. Draft deficiency responses, co-ordinate with CFTs, track the action items and review the documents for deficiency response. Display ability for timely response to deficiencies Demonstrate the ability to communicate the essential requirements to CFTs. Provide all the launch sheets and tech-packs, to facilitate timely launch of products. Support commercial team with tender related documents. Archive the submissions, responses, and other data in product folder. Qualification M Pharm/Masters in science Experience : 10 -15+ years Handing the Customer Audits and MoH Audits at our Manufacturing sites. Technical Skills Understanding of Good Manufacturing practice/Quality Systems. Understanding of product development, manufacturing processes, Intellectual Property and quality. Experience in handling various dosage forms like solid orals and sterile dosage forms. Sound knowledge of International Council for Harmonisation (ICH) / European Medicines Agency (EMA) guidelines on submission requirements and basic understanding of global regulatory affairs including United States Food Drug Approval requirements. Behavioral Skills Excellent communication and interpersonal skills. Efficient Leader and a good collaborator. Effective planning and high level of performance orientation. Strong analytical and problem-solving abilities. Additional Information

Hi, Greetings from Biophore !! We are hiring for Formulation IPM Department . Please go through the JD . Patent landscapes preparation/review for USA, EU, CA, and Row markets. Patent clearance or FTO evaluation on formulation strategies. Patent filing and prosecution for India, US, EU and other countries. Patent invalidations. IP evaluation during product selections for USA, EU, CA & RoW markets. Support to respond to IP queries from cross-functional departments. Tracking concern patents and applications or periodically tracking new supplements. Tracking patent litigations of Zenara drug products. IP support to Regulatory team by providing Patent or exclusivity certifications and PIL evaluations. Preparation of Global launch calendars across globe for critical drug products. IP support during discovery stage of Patent litigations. Preparation of NI and Invalidity notes and Attorney notes.

Dear Respected All, Greeting from Biophore India pharmaceutical Pvt Ltd. We have opening for Formulation IPM/IPR Department. Job Openings: 2 Nos Position : Executive / Sr Executive and Asst Manager Exp 3 - 10 Yrs. Job Location: Pashamylaram - Patancheruv (Telangana) Salary : As Per Company Norms Qualification: M .Pharm JOB DESCRIPTION: Formulation IPM/IPR Patent landscapes preparation/review for USA, EU, CA, and Row markets. Patent clearance or FTO evaluation on formulation strategies. Patent filing and prosecution for India, US, EU and other countries. Patent invalidations. IP evaluation during product selections for USA, EU, CA & RoW markets. Support to respond to IP queries from cross-functional departments. Tracking concern patents and applications or periodically tracking new supplements. Tracking patent litigations of Zenara drug products. IP support to Regulatory team by providing Patent or exclusivity certifications and PIL evaluations. Preparation of Global launch calendars across globe for critical drug products. IP support during discovery stage of Patent litigations. Preparation of NI and Invalidity notes and Attorney notes Ref to Friends or colleagues Please share me update resume: careers@biophore.com Total Exp : Current CTC: Exp CTC: Notice Period: Current Designation:

I. Division / Department: Legal/ IP Department II. Job Title: OSS Compliance and IP Engineer/ Counsel III. Level in the organization: AM/DM/MGR IV. Educational Qualification Essential: BE/ B Tech/M Tech in Computer Science/ Electronics Communication / Electrical Engineering with 2-8 years of experience in relevant Tech Industry - wireless telecom, software, semiconductors with patent analysis and OSS Compliance Desirable/ pref.: In-house experience preferred. V. Work Experience: a) Years of exp. Desired b) Nature of work exp. c) Any industry preference a) 2-9 years of work experience. b) 1. Should have experience in patent search databases such as Derwent Innovation, Orbit, etc. and on various analytics methodologies (novelty search, FTO, invalidation, technology search) and patent classification, related infringement analysis. 2. Candidate should have experience in retrieving legal/ prosecution related information from different Patent office s websites (such as USPTO PAIR and EP Register). 3. Should have experience in open-source software license validations/ Open-Source Compliance and Vulnerability Analysis. Experience in license obligations and compliance discussion of the OSS scans c) Experience in the field of Telecom architectures (WiFi, Bluetooth, 4G, 5G, LTE etc), wireless charging and audio/video technologies. d) Experience in Electric Vehicle hardware/software, Vehicular wireless communication systems, vehicular software architecture, connected cars, Battery system, ADAS, Telematics, Vehicle charging system, etc. VI. Key responsibilities 1. To educate, motivate engineers on creation and protection of intellectual property 2. To conduct ideation workshops and coordinate with various business functions for new idea generation/ submission 3. To work closely with RD engineers to review ideas and enhance the IDF conversion rate to patents 4. To evaluate ideas for patentability and to identify/draft key features for patent protection 5. To perform relevant patent study with respect to patentability, Freedom to operate, Invalidation, State of art search and infringement on different technologies 6. OSS Compliance VII. Competencies: Functional Should have attitude to proactively develop understanding of diverse technology areas apart from his / her technical background and strong interpersonal skills Must be able to possess good verbal and written communication skills, capable of effectively articulate ideas and actively listen to others to facilitate meaningful exchanges. Requires to be a self-starter with strong work ethics, ready to take initiatives, set personal goals, and displays persistence and resilience in the pursuit of organizational objectives. Needs a team player who thrives in collaborative environments and contributes to a positive team dynamic through constructive feedback and shared responsibilities. VIII. Any other specific job requirement: Good understanding of Automobile technology would be an added advantage.

Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies. With over 30 years of GLP compliance and certification, Eurofins Advinus serves diverse industries such as Biotech, Pharmaceutical, Biological, Agrochemical, Nutraceutical and Cosmetic. Eurofins Advinus is the only contract research organization (CRO) in India to have developed data in support of 90+ end-to-end IND enabling packages to be submitted to global regulators such as USFDA, EMA, MHRA, Health Canada and others. Role to manage team size of 1 to 3 scientists (M.Sc.) Good team player, should be able to lead the team of 1-3 scientist (M.Sc.) and monitor their day-to-day activities along with his own to complete the time bound tasks Strong interpersonal skill and managing cross functional teams Sound knowledge in synthetic/Medicinal chemistry Niche area chemistry experience is preferred Performing fundamental literature & patent searches related to project activities and develop alternative strategies Sound knowledge of scientific search engine such as SciFinder, Reaxys etc. Sound knowledge of structural elucidation and interpretation using analytical techniques such as NMR, IR, HPLC, GC, LC-MS etc. Good knowledge of laboratory safety and be a strong promoter of SHE activities in the lab Qualifications For M.Sc, 7-10 years of Discovery/Medicinal Chemistry R&D experience and for PhD, 2-4 years of experience in discovery/medicinal Chemistry CRO. Additional Information Excellent technical, problem-solving, writing, influencing and communication skills Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude. Demonstrative communication skills and confident in conveying information to internal customer

Support matters involving patent related information, mining, collation, analysis and transformation of complimentary pieces of information. You are expected to work collaboratively with engineering and attorneys in researching, analyzing and presenting key observations using analytics and presentation tools. You are expected to work on freedom to market, validity and landscape projects with a high level of diligence. You will apply significant product and technology knowledge of aligned business domain, and use the same to draft and prosecute patent applications. Key Responsibilities Design project scope (SOW) Deliver targets W.R.T quality Search and classify practices US, EP, India patent process Prosecute and draft portfolio Connect with customers Patent applications Product/technology knowledge Mining, collation, analysis WE VALUE Juggle many priorities and competing demands Some professional experience consisting of research, development and engineering (RD&E) Some hands-on experience on IP matters like patent search, analytics, prosecution, drafting, patent portfolio management Connect information to transform into enabling insights Clear and thoughtful communication skills Interpersonal skills and ability to handle pressure Accurately identify a variety of problems and issues Influence and collaborate effectively with diverse audience Exceptional written, oral and presentation skills

Hiring for leading chemical based research & manufacturing company!! Position: Patent Analyst / Specialist Location: Chennai 5 days working Only Work from office Must be qualified patent agent or certified IPR or patent related certification Role & responsibilities: Preparing IP opinions (patentability, FTO, invalidity) Providing insightful analysis of search results from various sources Keep an eye on technology, competition and geography through patent watches and disseminating the insights from patent watches to R&D and Business Assisting in patent oppositions and providing technical support to the enforcement activities through research and analysis of recent cases etc. Interested candidate can share updated resume to yogeswarisugumar@bdo.in along with below details. Total yrs of experience: Current location: Current CTC: Expected CTC: Notice Period:

Performing prior-art searches, including novelty search, freedom-to- operate/clearance search, validity/invalidity search, state-of the art search, patent landscaping, patent to product search, Infringement analysis/Evidence of Use Interacting with inventors & attorneys to comprehend and discuss invention disclosures or other IP related requirements Preparing invention disclosure forms (IDFs) Preparing deliverables based on custom templates

Roles and Responsibilities Job Description: Patent Searching Understand the technology of and conduct searches on various databases to ascertain the novelty/uniqueness of the idea/technology Patent Analytics and Landscaping Analyze patents in a particular domain to highlight the R&D trends, evolutions, alternatives and competitive intelligence in various technology domains Techno-commercial Analysis Research based on patents, scientific literature and products in a particular technology domain to generate insights into the value of the technology, IP protection and overlap between the products and patents Patent abstract skill is preferable Desired Candidate Profile BE with ECE/ Mechanical / EEE/ Biotechnology / Chemical / Mechatronics etc Job Benefits & Perks Salary with statutory benefits like ESI, EPF,Bonus, Insurance etc. You can refer friends for great opportunities

Job Description: Making of Landscape preparation and patent monitoring of drug products for the proposed Active Pharmaceutical Ingredients (API). Hand on experience in making Risk assessment for Genotoxic & Nitrosamine impurities in the APIs Preferably Hands on experience in Computational Toxicology with DEREK Nexus & SARAH Nexus software to prepare the report Knowledge in Regulatory guidelines on Impurities to fulfil DMF filing requirements Good experience in FTO analysis, Literature search , patents search to make the non-infringement report Drafting provisional and complete specification for patent application, filing in India and PCT based on R & D inputs .Making of patent evaluation & clearances reports for the proposed API for world wide. Taking of attorney opinions for proposed invalidity or non-infringement study wrt the proposed route of synthesis or products etc. Provide relevant inputs to CRD in development of patent non-infringing API process/polymorphs. Prepare responses for Customer queries relating to API for cross-functional departments such as RAD/ Marketing/BD and also for queries of external customers.. Maintaining the granted patents and patent applications filed in India and abroad for the in-house projects towards the payment of renewal fees by coordinating with the management. Preparing patent evaluation report for USA, Europe, Japan, and India markets for final API. For more details and to apply, please reach out at srinidhi@bvrpc.com

Identify, document, and develop know-how, inventions, and trade secrets generated across the company s functions. Manage and assist IP counsel in preparing and filing patent applications. Manage the technical responses to office actions during patent prosecution. Conduct prior art searches to assess patentability, freedom-to-operate, and patent landscapes. Build and improve internal systems to manage and streamline IP processes. Review draft contracts and RD agreements to ensure IP is protected. Work with the Head of IP to execute strategies and key actions to build and strengthen the company s IP portfolio. Educate and advise stakeholders on all IP matters, including preparing and delivering IP training. A degree qualified Chemical Engineer (preferred), Chemist, or Mechanical Engineer. Strong experience working with inventors to capture know-how, inventions, and trade secrets. 3-5 years experience in the preparation, filing, and prosecution of patent applications, especially in addressing office actions. Proven experience in patent searching, patentability and freedom-to-operate assessments, and patent landscaping. Experience with effectively managing external IP counsel. Experience safeguarding IP protection measures in commercial contracts and negotiating IP arrangements. Proactive approach, with the ability to independently manage tasks and contribute to team objectives. Excellent communication and interpersonal skills. Strong organizational skills. The opportunity to continue to develop both personally and professionally, in our rapidly growing company A brilliant company culture that encourages initiative, collaboration, and positivity at work Hybrid working - with the flexibility to work from home for up to 3 days a week 24 days holiday per year plus 10 gazette public holidays Everyone belongs at Carbon Clean We are passionate and committed to our people. Our aim is to build a diverse and inclusive movement: teams of forward-thinking people, with unique talents, skills, passions, and experiences. It s talent that matters to us and we encourage everyone to join us, whatever your gender identity, race, ethnicity, sexual orientation, age, life experience, or background. So please come as you are - we can t wait to meet you. We d be thrilled if you tick off all our boxes yet we also believe it s just as important we tick off all of yours. And if you think you have most of what we re looking for but not every single thing, go ahead and hit apply. We d still love to hear from you!