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Site Head

BDR Pharmaceuticals

Site Head

Skills

RComplianceRegulatory Compliance

2 months ago

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Important information


Contract type:

Permanent

Location:

Vadodara, Gujarat, India

Work mode:

Onsite

Published on:

18 August 2026

What they need


Job Description Site Head / Plant Head – API

Company: BDR Group
Location: Padra, Vadodara, Gujarat
Level: GM / Sr. GM / VP
Experience: 20+ Years
Function: API Manufacturing / Operations
Reporting To: Senior Management

Position Overview

We are looking for an experienced Site Head / Plant Head – API to lead the overall operations of our API manufacturing site at Padra, Vadodara.

The role requires a strong manufacturing leader with extensive experience in USFDA-regulated pharmaceutical manufacturing, particularly in Oncology/Cytotoxic API products and complex manufacturing processes.

Key Responsibilities

  • Lead the complete API manufacturing site, including Production, Quality, Engineering, EHS, Warehouse and other site functions.

  • Ensure achievement of production, quality, cost, productivity and delivery targets.

  • Drive a strong GMP and Quality culture across the site.

  • Lead and manage USFDA inspections/audits, including preparation, inspection handling and closure of observations.

  • Ensure compliance with USFDA, WHO-GMP, EU-GMP, CDSCO and other applicable regulatory requirements.

  • Manage large-scale API manufacturing operations involving:

  • Large-scale reactors

  • Hydrogenation

  • Spray Drying

  • Solvent handling and recovery

  • Complex chemical synthesis processes

  • Drive manufacturing excellence, process optimisation, yield improvement and reduction of batch failures/rejections.

  • Ensure effective CAPA, deviation, change control and investigation systems.

  • Partner with R&D, Quality, Regulatory, Engineering and Commercial teams for smooth technology transfer and scale-up.

  • Develop site manpower, leadership capability and succession planning.

  • Drive EHS, process safety and operational discipline across the plant.

  • Manage site budgets, CAPEX and operating costs.

  • Build a culture of accountability, continuous improvement and operational excellence.

  • Represent the site before regulatory authorities, customers and senior management whenever required.

Mandatory Experience & Qualifications

  • 20+ years of overall experience in API / Pharmaceutical manufacturing.

  • Proven experience as Plant Head / Site Head / Operations Head / senior manufacturing leader.

  • Must have worked in a USFDA-approved / USFDA-inspected pharmaceutical manufacturing facility.

  • Must have personally led or played a significant leadership role in USFDA audits/inspections.

  • Strong experience in Oncology / Cytotoxic API manufacturing.

  • Hands-on exposure to large-scale manufacturing processes involving:

  • Large-scale reactors

  • Hydrogenation

  • Spray Drying

  • Complex API synthesis

  • Strong understanding of GMP, regulatory compliance, quality systems and process safety.

  • Experience in managing large manufacturing teams and multiple site functions.

  • Strong commercial understanding of cost, productivity, yield and CAPEX management.

Preferred Profile

The ideal candidate should be a strong manufacturing and business leader, rather than only a functional production expert.

Preference will be given to candidates who have:

  • Managed a large API manufacturing site.
  • Experience with regulated markets, particularly the US market.
  • Successfully handled USFDA inspections with positive outcomes.
  • Experience in high-potency / oncology / cytotoxic APIs.
  • Managed significant CAPEX and capacity expansion projects.
  • Experience in building and developing second-line leadership.
  • Strong stakeholder management and communication skills.

Candidate Profile

Education: B.E./B.Tech/M.Tech in Chemical Engineering / Pharmacy / relevant technical discipline. MBA/PG qualification will be an advantage.

Experience: 20+ years

Industry: Pharmaceutical / API / Oncology / Specialty Chemicals

Level: GM / Sr. GM / VP

Location: Padra, Vadodara, Gujarat

Critical Requirement:
USFDA plant experience + leadership exposure in USFDA audits + Oncology/Cytotoxic API experience + large-scale reactor/Hydrogenation/Spray Drying exposure.

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