IPM Specialist

Good Health Can’t Wait

We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.

For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets).

‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency

Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.

Job Summary

• You will be responsible to perform search in various patent databases, screening of relevant patents/applications and prepare patent landscapes.
• You will be responsible to prepare the product reports including the Patent landscapes by exploring relevant regulatory databases.
• You will be responsible for Freedom to Operate Analysis to help in identifying any potential infringement on the intellectual property (IP) rights of another party.
• You will responsible to Non infringement analysis, Patentability analysis for different geographies like India, United State, Europe, Canada, Japan, China, South Korea with respect to product, polymorph, impurity, process screening and various exclusivities.
• You will be assisting Research and Development team in building polymorph, process, particle size, impurities and contamination for In-house development projects.
• You will be responsible for Supporting the Product Selection & Portfolio teams with necessary IP diligences 
• You will be responsible for Identification of prior arts to support building invalidation grounds for blocking patents/applications. 
• You will be responsible to provide technical support to legal teams during litigation/patent oppositions. 
  

Qualifications

Educational qualification:

• Experience in Intellectual Property (IP) domain
• Skilled in infringement/invalidity analysis, freedom to operate, filing and prosecution, Market launch analysis.
• Experience in product Identification and selection in perspective of complex Injectable, inhalation, OSDs in different geographies.
• Sound knowledge of technologies used in various dosage forms.
• Experience in due diligence in different geographies US, Europe, Australia, Canada, Japan, India etc

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.
• People management skills.
  

Additional Information

About the Department

Integrated Product Development Organization

Benefits Offered