Apply now »

About Intas

Recruitment Fraud Disclaimer:

Intas Pharmaceuticals does not request or accept any fees during recruitment. If someone asks for payment on our behalf, it is a scam. Please report the incident to the local police or cybercrime unit. Your trust and safety are important to us.

Intas is a leading global pharmaceutical company specializing in the development, manufacturing, and marketing of pharmaceutical formulations. The mission of the company is to address unmet medical and societal needs through a fully integrated pharmaceutical value chain spanning across the world.

Through its subsidiaries, the International presence of Intas includes the following countries: over 85 worldwide, with some of the more important global markets like North America, Europe, Latin America, and the Asia-Pacific under the well-known brand name Accord Healthcare. The rapid expansion has been due to organic growth and strategic acquisitions alone, vindicating its position in some of the important major pharmaceutical markets across the world.

Intas follows high standards of quality, as reflected by products approved for leading global regulatory agencies including USFDA, MHRA, and EMA. Substantial in-house R&D capability, along with the beginning of a focus on highly advanced areas like Biosimilars and New Chemical Entities-Intas continues to push the frontiers of excellence in healthcare.

At Intas, our success is fundamentally built on the strength of our people. Our ongoing commitment is to attract and retain the best talent in the industry while fostering an empowering environment that encourages innovation and excellence. This approach ensures that every employee plays a meaningful role in driving both the company’s growth and advancements in global healthcare.

Job Title:  Assistant Manager - SCM

Job Requisitions No.:  19008
Job Description: 

Purpose of Job

  • On-time product launch rate (OTIF)
  • Cycle time reduction from product approval to commercialization
  • Cross-functional adherence to project timelines
  • Successful entry into target markets

Roles and Responsibilites

1. New Product Launch Project Planning & Execution

  • Manage detailed project plans for new product launches across export markets
  • Define timelines, milestones, and deliverables aligned with business goals
  • Track progress and ensure adherence to launch timelines

2. Cross-Functional Coordination

  • Act as a central point of coordination between:
  1. Regulatory Affairs
  2. Artwork / Studio Team
  3. Sourcing and Procurement
  4. IT and Technical assistance team
  5. R&D / Formulation Development
  6. Manufacturing / Supply Chain
  7. Quality Assurance and Quality Control
  8. International Marketing / Business Development
  • Drive accountability and timely completion of deliverables

3. Regulatory & Dossier Management

  • Collaborate with Regulatory Affairs to track progress of dossier review at Agency
  • Maintain awareness of country-specific regulatory requirements (USFDA, MHRA, EU, ROW markets, etc.)

 

Other Requirements

1. Product Development Oversight

  • Monitor development activities including:
  1. Tech transfer
  2. Exhibit / validation batches
  3. Stability studies
  • Ensure alignment with filing and launch timelines

2. Launch Readiness

  • Ensure commercial readiness including:
  1. Packaging development (multi-country compliance)
  2. Artwork approvals
  • Support go-to-market strategies in coordination with business teams

3. Risk Management

  • Identify project risks and bottlenecks proactively
  • Develop mitigation strategies to avoid delays in launch timelines

4. Stakeholder Communication

  • Provide regular status updates to reporting manager
  • Prepare dashboards and reports on project progress, risks, and critical milestones

5. Portfolio & Pipeline Management

  • Support prioritization of pipeline products based on market potential and feasibility
  • Maintain visibility of the entire launch pipeline across geographies

Qualification Required

  • Bachelor’s/master’s in pharmacy (MBA preferred)

Skill Required

  • Strong project management skills (PMP® from PMI certification preferred)
  • Exposure to regulated markets (US, EU, UK, Canada) is highly preferred
  • In-depth knowledge of pharmaceutical production and regulatory pathways
  • Excellent stakeholder management and communication skills
  • Ability to manage multiple projects simultaneously
  • Problem-solving and risk mitigation capabilities
  • Proficiency in project management tools preferred (MS Project, Smartsheet, Excel dashboards)
  • Proficiency in SAP IBP, MS Power BI preferred
  • Strong analytical and planning skills
Location: 

Head Office, Ahmedabad, GJ, IN, 380054

Travel:  0% - 25%

Life at Intas Pharmaceuticals

For over three decades, Intas has thrived due to the exceptional talent of its people. Our growth is fueled by a dynamic environment that nurtures individual potential while fostering collaboration and collective success. We believe that when diverse skills and perspectives unite under a shared purpose and value system, we can achieve remarkable outcomes, driving innovation and excellence across the pharmaceutical landscape.
Date:  17 Oct 2026

Apply now »