Overview

Hiaan Pharma Pvt. Ltd. embarked on a significant greenfield project—a state-of-the-art GMP manufacturing facility designed to produce sterile products for global markets. The project included a complete technology transfer from an existing facility and the construction of a new GMP-compliant filling line. This high-stakes initiative demanded a specialized workforce with deep expertise in pharmaceutical startups and the adaptability to thrive in a fast-paced, ever-evolving environment.

Recognizing Baker Finn’s reputation for delivering high-caliber talent with greenfield and startup experience, the client partnered with us to source a multidisciplinary team to guide the project from the planning phase through to commercial production.

Project Objectives

  • Deliver a fully operational EU-GMP facility on time and within budget, aligned with regulatory requirements.
  • Transfer technology, processes, and knowledge from the existing UK facility to the new site seamlessly.
  • Build and validate a new sterile filling line to support commercial-scale production.
  • Recruit a dynamic workforce capable of thriving in a greenfield startup environment.

The Importance of Greenfield Experience

Greenfield projects present unique challenges that demand more than technical expertise. The fast-paced, high-pressure environment requires individuals who can adapt to fluid roles, embrace hands-on responsibilities, and collaborate across functions to overcome unforeseen obstacles. Professionals with prior startup experience bring an invaluable “roll-up-your-sleeves” mentality, making them critical to the success of such projects.

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Our Role

Hiaan Pharma became the client’s trusted partner for sourcing specialized talent. Our team’s deep understanding of pharmaceutical capex greenfield builds and track record of finding professionals with startup experience allowed us to deliver exceptional value.

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Key Roles Provided

Hiaan Pharma became the client’s trusted partner for sourcing specialized talent. Our team’s deep understanding of pharmaceutical capex greenfield builds and track record of finding professionals with startup experience allowed us to deliver exceptional value.

Commissioning, Qualification, and Validation (CQV) Experts

1. Commisining one

  • Executed qualification protocols (IQ, OQ, PQ) for utilities, equipment, and systems.
  • Ensured the facility met all regulatory standards and readiness for GMP production.

2. Tech Transfer Specialists

  • Facilitated seamless technology transfer from the UK site, ensuring knowledge retention and minimizing disruption.
  • Adapted existing processes to align with the new facility’s design and capabilities.

3. Project Managers with Greenfield Expertise

  • Oversaw construction timelines, resource allocation, and stakeholder communication.
  • Addressed challenges inherent to startup projects, including evolving scope and tight deadlines.

4. Process Engineers

  • Supported sterile filling line design, installation, and optimization.
  • Worked cross-functionally to troubleshoot and refine production workflows.

5. Construction and Startup Generalists

  • Professionals with the ability to take on multiple roles in a fast-paced startup environment.
  • Provided flexibility and problem-solving skills essential for the project’s dynamic needs.