JOB DETAILS

Delivery Manager – API (Process R&D)

CompanyDr Reddy's Laboratories Limited
LocationBachupalle
Work ModeOn Site
PostedJune 3, 2026
About The Company
Established in 1984, we are a global pharmaceutical company headquartered in Hyderabad, India. Driven by our purpose of ‘Good Health Can’t Wait’, we work to provide access to affordable and innovative medicines. We offer a portfolio of products and services including APIs, generics, branded generics, biosimilars and OTC. Our major markets include USA, India, Russia & CIS countries, China, Brazil and Europe. As a company with a history of deep science that has led to several industry firsts, we continue to plan ahead and invest in future growth drivers such as access to novel molecules, digital therapeutics and consumer healthcare. As an early adopter of sustainability and ESG actions, we released our first Sustainability Report in 2004. Our current ESG goals aim to set the bar high in environmental stewardship; access and affordability for patients; diversity; and governance. For more information, log on to: www.drreddys.com. Caution Notice: Dr. Reddy's has been made aware of candidates receiving fraudulent job opportunities from unauthorised recruiting agencies or people impersonating Dr. Reddy's leaders. These fraudulent jobs may be advertised on employment sites or mimic our careers site and company email addresses. Please know that Dr. Reddy's Laboratories has no affiliation or connection to these situations. Dr. Reddy's (and its associated/group companies) follows a formal recruitment process through its own HR department. Please report immediately in case you suspect a fraudulent job. You may raise your concern by: Accessing https://drreddys.ethicspoint.com.  Calling on the hotline number. List of hotline numbers are available in https://drreddys.ethicspoint.com. The hotline is available 24x7 in multiple languages.  Writing to complianceofficer@drreddys.com or chiefombudsperson@drreddys.com. For our community guidelines on LinkedIn, please visit: https://shorturl.at/LTvNZ
About the Role

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.

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Job Description

About the Role


As Delivery Manager – API, you will lead the full spectrum of drug development, overseeing the design, development, scale-up, and approval of APIs including complex molecules like peptides, Oligonucleotides and ADC. This role demands deep expertise in Upstream viz. Solid-phase, Liquid and hybrid peptide synthesis and downstream viz. purification and isolation techniques viz. Lyophilization, spray drying, Characterization, and regulatory aspects.
You will collaborate cross-functionally to deliver IP-driven, globally compliant, and commercially viable peptide products — accelerating development timelines while ensuring safety, scalability, and sustainability.

Role expectations:
• API Process Development: Drive the design and optimization of peptide synthesis (SPPS, LPPS, hybrid), conjugation chemistry, Oligonucleotide synthesis, ADCs and downstream purification (HPLC, Ultrafiltration, lyophilization).
• Early-to-Late-stage Development: Lead the molecule’s journey from preclinical stage through clinical scale-up to tech transfer and commercial manufacturing.
• Quality by Design (QbD): Implement QbD principles, risk assessments, and DoE strategies to build robust, reproducible processes.
• CMC Strategy & Regulatory Alignment: Provide strategic input and documentation for DMF, and ANDA submissions in major regulatory markets (US, EU, ROW).
• Analytical Support: Collaborate with analytical development teams to establish validated, peptide-specific analytical methods (purity, identity, aggregation, and stability).
• Scale-up and Technology Transfer: Drive the scale up of the designed process by deploying suitable technology and guide the CFTs for seamless execution
• Peptide-Specific Challenges: Tackle technical complexities like peptide solubility, aggregation, stereoisomerism, sequence-specific stability, and scale-up of long-chain peptides or cyclic analogues.
• Technology Scouting & Innovation: Identify and deploy emerging peptide technologies (microwave-assisted SPPS, flow synthesis, peptide–drug conjugates).
• Lifecycle & Cost Management: Optimize synthetic routes for cost, purity, and process yield across the lifecycle.

Qualifications

• PhD in Organic/Medicinal Chemistry, Peptide Chemistry, or related field
• 15+ years of experience in API development, with significant focus on peptides, Oligonucleotide and ADC development
• Proven expertise in solid-phase synthesis, downstream processing, analytical method development, and scale-up
• Familiarity with GMP manufacturing, global regulatory guidelines (ICH, USFDA, EMA), and CMC dossier preparation
• Demonstrated leadership in cross-functional environments, tech transfer, and regulatory interactions

Additional Information

About the Department - IPDO

At the core of our R&D prowess is the Integrated Product Development Organisation (IPDO) at
Bachupally, Hyderabad, India. The expansive campus of IPDO houses several laboratories powered by
a diverse talent pool of scientists from leading institutions around the world. Our product development
efforts drive a portfolio of more than 1,000 products, enabled by our robust R&D team consisting of
more than 190 doctorates. We integrate our deep science capabilities and cutting-edge technology to
develop innovative, accessible, and affordable therapies for patients worldwide. We are a sciencedriven,
innovation-focused pharmaceutical company committed to accelerating access to healthcare
solutions globally. We have end-to-end capabilities in API, Formulations, Clinical, Intellectual Property,
and Regulatory Affairs. We serve 55+ markets, including the USA, Canada, Europe, China, LATAM,
ASEAN, and all Emerging Markets, with innovative and generic products ranging from APIs, Oral
formulations, Parenteral (Injectables, Ophthalmics), and other dosages.
Future Focus on Pharmaceutical Innovation

" Benefits Offered

At Dr. Reddy's, we actively help to catalyze your career growth and professional development through personalized 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/#!/.

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  • Job Family: Research & Development
  • Sub Job Family: Process R&D - API
  • Preferred type of working: On-Premise
  • Years of Experience: 20 +
  • Business unit: IPDO
  • Key Skills
    API Process DevelopmentPeptide SynthesisOligonucleotide SynthesisADC DevelopmentDownstream PurificationQuality By DesignCMC StrategyTechnology TransferScale-upRegulatory ComplianceOrganic ChemistryMedicinal ChemistryHPLCLyophilizationDoE StrategiesAnalytical Method Development
    Categories
    Science & ResearchHealthcareManufacturingEngineeringManagement & Leadership
    Benefits
    Joining & Relocation SupportMaternity & Paternity BenefitsLearning And Development OpportunitiesMedical CoverageLife Coverage
    Job Information
    📋Core Responsibilities
    Lead the full spectrum of drug development for APIs, focusing on the design, scale-up, and approval of complex molecules like peptides and ADCs. Collaborate cross-functionally to deliver globally compliant, commercially viable products while optimizing synthetic routes for cost and yield.
    📋Job Type
    full time
    📊Experience Level
    10+
    💼Company Size
    32398
    📊Visa Sponsorship
    No
    💼Language
    English
    🏢Working Hours
    40 hours
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