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Salary
≈ $15k – $41k per year (Estimated)
Location
In office (Mumbai)
Seniority
Senior · 14+ years exp

Confirmed on the employer's own hiring board on Sep 30, 2026. First seen by Alion on Aug 29, 2026.

Overview
Company
Impact
Profile match
Headquartered in Mumbai, India, Sun Pharmaceutical Industries Limited (Sun Pharma) is a global specialty generic pharmaceutical enterprise and the largest pharmaceutical company in India. The company manufactures and markets a broad portfolio of generic and branded generic pharmaceuticals, complex drug formulations, over-the-counter (OTC) products, and active pharmaceutical ingredients (APIs) across key therapeutic areas such as dermatology, ophthalmology, psychiatry, cardiology, and oncology. Supported by an extensive global manufacturing footprint and robust R&D capabilities, it delivers high-barrier-to-entry and affordable medicines to healthcare systems in more than 100 countries worldwide.

Job Title:

Manager / Sr.Manager CMO

Business Unit:

Global Quality & Compliance

Job Grade

G10 -Manager-1 / G9B (SM-2)

Location :

Mumbai

At Sun Pharma, we commit to helping you “Create your own sunshine”- by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.

Are You Ready to Create Your Own Sunshine?

As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”

Job Summary :

To ensure that SUN Pharma Quality and Compliance Standards, and applicable global regulatory authorities’ requirements are met and that all CMOs achieve, maintain and improve the adequate level of compliance, through “Quality Oversight” for USA Markets.

Key responsibilities:

  • Participate in the initial evaluation of Contract Manufacturing Organizations (CMOs).
  • Should have experience in managing manufacturing operations at External contract manufacturing sites.
  • Lead, oversee, approve & monitor Quality Management System (QMS) elements reported by CMOs, including change control, deviations, incidents, out of Specification (OOS)/out of Trend (OOT) results, and complaint investigations targeting for injectable & OSD products manufactured for emerging markets.
  • Ensure that the CMO operations are in compliance with global regulatory standards (FDA, EMA, WHO, ICH) and SUN internal quality systems.
  • Review and maintain quality agreements with CMOs to ensure compliance and quality standards.
  • Review the batch records, validation protocols, and analytical reports for sterile injectable formulation for USA Market.
  • Support for the project management team during the execution of exhibit/scale-up batches at the CMO site.
  • Collaborate with cross-functional teams including Regulatory Affairs, Manufacturing, and Supply Chain to ensure product quality and compliance.
  • Drive continuous improvement initiatives and inspection readiness at CMOs
  • Minimum 13 years of pharmaceutical QA experience, with strong exposure to injectable manufacturing operations for Regulated markets.

Travel Estimate

Job Requirements

Educational Qualification

M.Sc / B.Pharm / M.Pharm

Experience

Tenure: 14+ years of Industry experience and working knowledge in regulatory environments. Experience in handling quality managements systems.

Your Success Matters to Us

At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!

Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).

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