Regulatory Affairs Analyst

Company Description Dr Reddy s Laboratories Ltd is a leading multinational pharmaceutical company based across global locations Each of our 24 000 plus employees comes to work every day for one collective purpose to accelerate access to affordable and innovative medicines because 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 We are seeking a detail-oriented Regulatory Affairs professional to join our team in Hyderabad India In this role you will play a crucial part in ensuring our organization s compliance with regulatory requirements and supporting the development and maintenance of regulatory strategies Preparing the NDA Registration application for submission to Emerging Markets communicating with regulatory agencies and managing the regulatory review process Ensuring that the drug is approved for marketing in a timely manner and that it meets the regulatory requirements for commercialization Timely update and preparation of dossier and documents as well as responses to the queries raised by regulatory agencies Registration application preparation including administrative documents and GMP audit support for global markets Preparation of gap analysis for the registration in Emerging Markets Review assessment and establishing tracking effective change control management coming for regulatory review and approval Work with a team of regulatory affairs experts of various countries to ensure that the NDA is submitted correctly and meets respective regulatory agencies requirements Participate in due diligence activities for innovative pipeline assets identify necessary clinical and regulatory requirements needed for regulatory approval in Emerging Markets Work closely with Cross-functional teams for review of Normative Document ND and ensure timely submission of samples for PQC testing Identify and assess regulatory risks mitigations opportunities and contingencies Liaise closely with the CMC and clinical teams to ensure all regulatory requirements are met and all information needed for ongoing documentation and registration is produced Review Clinical trial protocols Clinical study report contents and approval requirements to facilitate CT NOCs and marketing authorization approval by regulatory agencies Ensure effective planning preparation and timely submission of INDs CTAs NDAs and other regulatory documents and applications as required Provide strategic direction and content input on product labelling Ensure adherence to and continuous improvement of standards processes and guidelines for regulatory submissions of innovative products End to End RA function support for allocated asset country Guide by providing regulatory strategy for complex molecules asset Provide functional support to RA and CFT members to meet the current regulatory requirements and guidelines in order to secure the acceptances approvals and launches of innovative assets Accountable for decisions and appropriateness of submission documentation to support successful NDAs MAAs Dossiers and other submissions to various agencies Deficiency Management Coordinates and Collaborates with multi-disciplinary matrixed teams in relation to pending deficiencies to meet timelines with appropriate prioritization Guides RA and CFT members by providing appropriate regulatory strategies to ensure the accuracy and adequacy of the response Support the Launch team - Supports the launch team by providing necessary regulatory strategies inputs and decisions for the proposed changes if any within the regulatory framework thus safeguarding the regulatory compliance and the launch of the product Ensures the smooth transition of the approved and launched products to the Life-cycle Management LCM Process along with the history of approval process Qualifications Masters in Pharmacy Well-versed with the new drug development process and understanding of scientific content and complexities related to NCEs Thorough understanding of the regulatory agencies requirements of various countries for NDAs MAAs including the required format and content of the application Around 5 years of experience in regulatory domain with knowledge of NDAs MAAs submission to various Health Authorities HAs and associated processes Proficient in eCTD requirements and Hands-on experience of submitting registration application in eCTD format to the HAs Fundamentals on the following is necessary Understanding of Good Manufacturing practice Quality Systems Experience in incoming outgoing and product quality Knowledge of Intellectual Property Rights Additional Information About the Department Integrated Product Development Organisation We integrate our deep science capabilities and cutting-edge technology to develop innovative accessible and affordable therapies for patients worldwide We are a science-driven innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world We have End to end capabilities in API Formulations Clinical Intellectual Property and Regulatory Affairs We are serving 55 markets including USA Canada Europe China LATAM ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients API Oral formulations Parenteral Injectables Opthalmics Other dosages Our product development efforts drive a portfolio of more than 1 000 products Enabled by our robust R D team consisting of more 200 scientists and functional experts and more than 150 doctorates we have filed 1 071 patents and also published over 1 000 papers for peer review over the years 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 https careers drreddys com