Specialist - IPM

Job Summary
We are looking for a dynamic Specialist to join the Biologics IPM (Intellectual Property Management) Team, adept in deriving the LOE dates for pipeline Biological products. The ideal candidate will prepare non-infringement opinions, facilitate development of alternate process and formulations, and drive the filing and prosecution of patent applications, aiming to alert the organization to potential 3rd party IP threats and enable early product launches in regulated and key emerging markets.
Roles & Responsibilities
• You will be responsible for designing and implementing search strategy to identify the patents relevant to a product/process.

• You will be responsible for preparing and maintaining database of all 3rd party patents that might block the launch of product in countries of interest.

• You will prepare detailed landscape and freedom to operate reports on pipeline products/process.

• You will interact closely with the R&D (Research and Development) team in developing an alternate process, to work around the blocking patents.

• You will be responsible for identifying patentable inventions from in-house R&D process development, performing patentability search, and drafting patent applications.

• Your role includes prosecuting the patent application in various patent offices.

• Your responsibilities include performing prior art searches and providing other inputs required for preparation of invalidation grounds for blocking patents.

 • Your responsibilities include tracking patent application prosecution and patent litigation in various jurisdictions, changes in patent/regulatory laws and evaluating their impact on the launch plans of pipeline products.

• Your responsibilities include keeping abreast of evolving patent jurisprudence and actively participating in continued learning initiatives in the team.

Educational qualification: M.Sc./Ph.D. in Biotechnology or allied Life Sciences subjects; a qualified Indian Patent Agent and/or PG Diploma in patents law is preferred
Minimum work experience : 6 to 10 years’ experience in handling biopharmaceutical IP issues
Skills & attributes:
Technical Skills
• Proficiency in devising IP search strategies and conduct comprehensive searches.
• Capability to identify blocking IP and contribute to building an effective IP strategy.
• Experience in preparing various IP reports, such as FTO, patentability, and other relevant analyses.
• Ability to prepare preliminary patent drafts, manage the filing process, and engage in patent prosecution activities to protect IP.
• Skill in tracking the technology and IP space, providing Competitive Intelligence (CI) inputs to support strategic decision-making.
• Ability to support in securing other IPRs (such as Design, Trademark, and Copyright), publication activities, and CI initiatives related to IP.
Behavioural Skills
• Proficiency in addressing complex challenges through analytical thinking and effective problem-solving.
• Effective communication and interpersonal skills, fostering collaboration and understanding.
• Ability to identify opportunities and take prompt action, displaying a proactive approach.
• Ability to think strategically and critically, connecting the dots to innovate for unmet needs.
• Ability to acquire new skills and is a quick learner, excelling in deliverables.
• Ability to connect with people and is result-oriented, achieving outcomes effectively.

About the Department
Biologics
Currently operates in the Global Biosimilars business - a segment that is poised for attractive and sustained growth over the next 10–15-year time horizon.
With a robust portfolio of biosimilar products across key therapeutic areas, covering ~US$80+ Bn in innovator sales – future business pipeline covers a variety of product classes and therapy areas, and new modalities. Fully integrated organization with over two decades of experience in developing, manufacturing and commercializing multiple biosimilar products.
With a Product Development engine that has end-to-end capabilities – in-house clone development, upstream and downstream process development, bioanalytical development and proprietary formulation.
Supported by a Clinical and Regulatory team with experience in executing complex biosimilar programs with innovative global trial designs.
We have a proven experience in commercial-scale manufacturing across a variety of technology platforms with global quality standards and a highly competitive cost structure
Rich experience of commercializing high-quality biosimilars in multiple markets with over 900,000 patients having benefited from our products till date.
Benefits Offered
At Dr. Reddy’s we actively help to catalyse 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