Dr Reddy's Laboratories Limited logo
Director / Lead External Manufacturing
full-timePrinceton

Summary

Location

Princeton

Type

full-time

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About this role

Company Description

At Dr Reddy's "Good Health Can't Wait"

By joining Dr Reddy’s, you will contribute to making the breakthroughs of tomorrow a reality today! From making medicines more affordable to discovering innovative treatment options to satisfy unmet medical needs, we are dedicated to helping people lead longer and healthier lives. We are seeking dynamic and energetic individuals ready to inspire, ready to make a difference for their community and every community.

Diversity, Equity & Inclusion
At Dr Reddy’s, we are deeply committed to building a diverse, equitable and inclusive workplace where everyone belongs and is valued for their contributions to the team.  We are most interested in finding the best candidate for the role and are open to exploring candidates with a less traditional background.

Job Description

We are seeking a Director / Lead External Manufacturing to lead operations for North America, to ensure reliable supply of commercial products and support new product launches. The position manages relationships with Contract Manufacturing Organizations (CMOs) and Contract Packaging Organizations (CPOs), driving operational excellence, compliance, and cost efficiency while collaborating with internal stakeholders across Quality, Supply Chain, Regulatory, Technical Services, and Commercial teams.

Responsibilities:

Supply Assurance & Operations

  • Coordinate with CMOs/CPOs to ensure on-time, in-full (OTIF) delivery of cGMP compliant, and quality reviewed and released FG and Bulk drug products to customers and markets
  • Determine supply priorities through interaction with the Global Supply chain and External Manufacturing (EM) team members on a regular basis and communication of these priorities and changes to the relevant CMO/CPO
  • Understand CMO’s capacity constraints, bottlenecks, material shortages etc. in the short medium and long term, aid resolution of these constraints & escalate to the supply chain management as needed
  • Manage the commercial product lifecycle, including raw material changes, artwork updates, process revalidations, packaging changes, and shelf-life extensions
  • Prepare and provide accurate monthly forecasts, purchase orders, and stock-transfer orders to the CMO’s manufacturing sites in-order to meet forecasted demand and target inventory/MOH levels
  • Lead/participate in cross-functional due diligence teams to assess new business opportunities and potential capabilities of a new CMO
  • Review, approve, and submit CMOs invoices for timely payments

Compliance & Documentation

  • Ensure all compliance-related documents, such as batch records, COC/COA, etc., for each order are accurate and available for Quality Assurance review and release
  • Arrange permits, state licenses, quality agreements, and service agreements to maintain GMP/GDP compliance
  • Review of CMO related change controls to understand the supply chain impact. Work closely with QA, regulatory, commercial and packaging teams to facilitate risk assessment & impact, along with approval process for the changes proposed/implemented at the CMO
  • Ensure the complete set of shipping documents is provided by the CMO/CPO including packing list, commercial/custom invoice, certificate of origin, BOL/AWB/HWB, EPICS file and all approved copies of COC’s and COA’s at the time of shipment

Data & Systems

  • Facilitate set up and validate material and vendor master data in SAP and related systems
  • Support the entire order-to-commercial cycle with proactive issue resolution
  • Liaison and support DSCSA compliance and serialization requirements with CMO’s Serialization team, collaborate with internal IT, and 3PL warehouse to ensure complete and timely implementation of GS1 EPCIS process to meet FDA requirements for new product launches and CMO’s on-boarded

Continuous Improvement

  • Lead cost optimization projects with partners to improve throughput and efficiency
  • Drive initiatives to mitigate supply chain risks and enhance operational resilience
  • Participate and drive Alternate Vendor Development (AVD) projects for evaluating and validating new API, excipients and RM vendors for dual-sourcing, cost savings and reliability optimization

Qualifications

Educational qualification: Postgraduate degree with specialization in Operations Management, Supply Chain Management or related field

Minimum work experience: 10+ years of experience in cGMP pharmaceutical manufacturing or supply chain operations

Skills & attributes:

  • Proven experience in contract manufacturing management in an international environment
  • Strong operational expertise in pharmaceutical supply chain and generics business model
  • Proficiency in SAP, MS Office, and MS Project
  • Demonstrated ability to work with urgency, meet timelines, and ensure compliance
  • Excellent leadership and relationship-building skills across multicultural, multilingual environments
  • Strategic thinking with strong execution capability
  • Negotiation and alliance management skills
  • Problem-solving and proactive risk mitigation
  • Ability to influence across functions and geographies

Incumbent must be a U.S. citizen or lawful permanent resident of U.S. or otherwise authorized to work in the U.S. without requiring visa transfer or sponsorship, now or in the future.

Incumbent should be willing to work in person from our Princeton, NJ office

Additional Information

Dr.Reddy's Laboratories offers a competitive total rewards package including base salary determined on the basis of role, experience, skill set and location. Additionally, employees are eligible for an annual discretionary bonus, and benefits including comprehensive health care coverage, retirement savings plan and leave benefits. Additional details about total compensation and benefits will be provided during the hiring process.

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.

Equal Opportunity Employer

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against based on disability.

For more details, please visit our career website at https://careers.drreddys.com/#!/

  • Job Family: Supply Chain Management
  • Sub Job Family: External Manufacturing
  • Preferred type of working: Hybrid
  • Years of Experience: 6 - 12
  • Business unit: NAG
  • Other facts

    Tech stack
    Contract Manufacturing Management,Pharmaceutical Supply Chain,Operational Expertise,SAP,MS Office,MS Project,Leadership Skills,Relationship Building,Strategic Thinking,Negotiation Skills,Problem Solving,Risk Mitigation,Influencing Skills

    About Dr Reddy's Laboratories Limited

    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 [email protected] or [email protected].

    For our community guidelines on LinkedIn, please visit: https://shorturl.at/LTvNZ

    Team size: 10,001+ employees
    LinkedIn: Visit
    Industry: Pharmaceutical Manufacturing
    Founding Year: 1984

    What you'll do

    • The Director / Lead External Manufacturing will coordinate with CMOs/CPOs to ensure timely delivery of compliant products and manage the commercial product lifecycle. The role also involves leading cost optimization projects and driving initiatives to enhance operational resilience.

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    Frequently Asked Questions

    What does a Director / Lead External Manufacturing do at Dr Reddy's Laboratories Limited?

    As a Director / Lead External Manufacturing at Dr Reddy's Laboratories Limited, you will: the Director / Lead External Manufacturing will coordinate with CMOs/CPOs to ensure timely delivery of compliant products and manage the commercial product lifecycle. The role also involves leading cost optimization projects and driving initiatives to enhance operational resilience..

    Why join Dr Reddy's Laboratories Limited as a Director / Lead External Manufacturing?

    Dr Reddy's Laboratories Limited is a leading Pharmaceutical Manufacturing company.

    Is the Director / Lead External Manufacturing position at Dr Reddy's Laboratories Limited remote?

    The Director / Lead External Manufacturing position at Dr Reddy's Laboratories Limited is based in Princeton, New Jersey, United States. Contact the company through Clera for specific work arrangement details.

    How do I apply for the Director / Lead External Manufacturing position at Dr Reddy's Laboratories Limited?

    You can apply for the Director / Lead External Manufacturing position at Dr Reddy's Laboratories Limited directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about Dr Reddy's Laboratories Limited on their website.