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Head- CDMO

Mumbai Permanent View Job Description
Lead CDMO strategy by identifying, evaluating, and managing contract manufacturers to ensure quality, compliance, and timely production of generics. Collaborate across regulatory, R&D, and logistics teams to optimize the supply chain, ensure regulatory adherence, and mitigate outsourcing risks.
  • Opportunity to join the founding team of the pharma arm of a renowned company
  • Opportunity to work with a rapidly growing life science company in India

About Our Client

Our client is leading business and investment house, actively investing in a diverse range of ventures across multiple industries.

Job Description

The key responsibilities include:

1. CDMO Strategy and Vendor Management:

  • Identify and evaluate potential CDMOs: Research and establish partnerships with contract manufacturers capable of meeting production requirements for generics.
  • Evaluate performance: Regularly assess the CDMO's performance to ensure they meet quality standards, timelines, and cost targets.



2. Regulatory Compliance and Quality Assurance:

  • Work with regulatory affairs: Collaborate with the regulatory team to ensure that the product manufactured by the CDMO complies with national and international regulations (e.g., CDSCO, USFDA, EMA).
  • Compliance audits: Conduct regular audits and inspections at the CDMO sites to ensure manufacturing practices align with regulatory and company standards.
  • Ensure product registration: Support the regulatory team in product filings and ensuring that manufacturing sites are registered with the relevant authorities.



3. Supply Chain and Logistics Management:

  • Supply chain optimization: Identify opportunities to improve supply chain efficiency, reduce lead times, and ensure timely deliveries from CDMOs.
  • Cross-department collaboration: Work closely with R&D, regulatory, marketing, and logistics teams to ensure smooth coordination and timely delivery of products.
  • Identify and mitigate risks: Proactively manage potential risks related to outsourcing production, including regulatory risks, quality risks, and supply chain disruptions.

The Successful Applicant

The ideal candidate would have:

  • Bachelor's/ Master's degree or MBA in Operations Management, Pharmaceutical Management, or Supply Chain (preferred).
  • Minimum 15 years of experience in the pharmaceutical industry, with a proven track record of working with CDMOs and managing outsourced manufacturing operations.
  • Hands-on experience with GMP, regulatory compliance, and quality control in pharma manufacturing.
  • Ability to lead cross-functional teams and manage multiple stakeholders and build systems and processes from the ground up.
  • High attention to detail and a commitment to ensuring compliance and quality at all stages of the production process.

What's on Offer

This role offers an exciting opportunity to be a founding member of a high-growth pharma startup with a collaborative, fast-paced culture and attractive rewards.

Quote job ref
JN-052025-6738745

Job summary

Function
Healthcare & Life Sciences
Sub Sector
Manufacturing / Quality
What is your area of specialisation?
Healthcare / Pharmaceutical
Location
Mumbai
Job Type
Permanent
Job Reference
JN-052025-6738745

Diversity & Inclusion at Michael Page

We don't just accept difference - we celebrate it. We encourage applicants from all backgrounds to apply for this role and are committed to building inclusive, diverse workplaces where everyone can thrive. If you require any support or reasonable adjustments during the recruitment process, please let us know.