Analyst Regulatory Affair at Dr Reddy's Laboratories Limited

Bachupalle, Andhra Pradesh, India -

Full Time

Start Date

Immediate

Expiry Date

25 Jan, 26

Salary

0.0

Posted On

27 Oct, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Regulatory Requirements, Product Development, Manufacturing Processes, Intellectual Property, Quality, GxP Documentation, Communication Skills, Interpersonal Skills, Collaboration, Planning, Performance Orientation, Analytical Skills, Problem-Solving Skills

Industry

Pharmaceutical Manufacturing

Description

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. Job Description Job Summary We are seeking a detail-oriented Analyst in Regulatory Affairs to oversee Emerging Markets procedures - ANZ , handle Marketing Authorization Application, and ensure compliance with regulatory guidelines. Responsibilities include managing chemistry, manufacturing, and controls (CMC) documentation, addressing deficiency letters, contributing to regulatory strategy development, and facilitating effective communication with stakeholders for successful product launches and regulatory compliance. Roles & Responsibilities • You will be responsible for handling the end-to-end various Registration in ANZ and EM • You will be responsible for preparation, review and submission of Dossier in ANZ and Emerging Markets as per the applicable regulatory guidance in Emerging Markets. • You will be responsible authoring high-quality chemistry, manufacturing, and controls (CMC) documentation for health authorities’ submissions, applying agreed CMC global regulatory strategies, assuring technical congruency and regulatory compliance throughout the project lifecycle. • You will be responsible to review of critical quality/regulatory documents like specifications, stability protocols, stability data, development report, justification reports etc. • You will be responsible for on time Response to deficiency letters. • You will be responsible for preparing Regulatory strategy notes, regulatory due diligence and gap analysis for leverage products. Evaluating and sharing the Regulatory Affair requirements with product development teams at the product introduction stage, performing regulatory due diligence and consolidated gap analysis for leveraging. • You will be responsible for identifying all open issues and anticipated questions on regulatory submission at respective stage of product development, Dossier filing and deficiency responses in consultation with team leads. • You will be responsible to review and closure of change control notifications (CRNs) for under development, under review and launch products in consultation with team lead. • You will be providing launch support w.r.t key regulatory decisions. • You will be responsible to interact with Internal and External stakeholders/customers and provide timely regulatory guidance on various issues. Qualifications Educational qualification: M Pharm Minimum work experience: 4-6 years of experience in ANZ Regulatory affairs Skills & attributes: Technical Skills Knowledge on Regulatory requirements. Understanding of product development, manufacturing processes, Intellectual Property and quality. Experience in GxP documentation Behavioral Skills Excellent communication and interpersonal skills. Efficient and a good collaborator. Effective planning and high level of performance orientation. Strong analytical and problem-solving abilities. 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/#!/

Responsibilities

The Analyst in Regulatory Affairs will manage the end-to-end registration processes in ANZ and Emerging Markets, ensuring compliance with regulatory guidelines. Responsibilities include preparing and submitting high-quality CMC documentation and addressing deficiency letters to facilitate successful product launches.