10 - 20 years

1 Lacs

Posted:2 days ago| Platform: Naukri logo

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Full Time

Job Description


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Role Summary

We are looking for an experienced and strategic Production Head to lead our manufacturing

operations in the medical device domain. The ideal candidate will have deep knowledge of

regulated production environments, strong people management skills, and a passion for driving

quality, safety, and efficiency. This role is critical to ensuring that our products meet global

standards and are delivered on time and within budget.

Key Responsibilities

  • Lead and oversee all daily manufacturing activities, ensuring production targets, timelines, and quality standards are met.
  • Develop and implement effective production strategies aligned with company goals.
  • Ensure full compliance with regulatory and quality standards, including ISO 13485, FDA21 CFR Part 820, and EU MDR.
  • Manage cleanroom operations and ensure adherence to safety and hygiene protocols.
  • Plan and optimize resource allocation including manpower, materials, and machines.
  • Implement and promote Lean Manufacturing, 5S, Six Sigma, and other process improvement techniques.
  • Coordinate with cross-functional teams such as Quality, R&D, Regulatory Affairs, SCM, and Maintenance.
  • Oversee preventive and corrective maintenance of production equipment and ensure minimal downtime.
  • Ensure documentation practices meet Good Manufacturing Practices (GMP), including DMR, DHR, CAPA, NCR, etc.
  • Train, mentor, and lead the production team to drive productivity and accountability.
  • Participate in internal, external, and regulatory audits.

Qualifications

  • Bachelors/Masters degree in Mechanical / Industrial / Biomedical Engineering or related field.
  • Certifications in Lean, Six Sigma (Green/Black Belt), or ISO 13485 are an advantage.

Experience

  • 12-20 years of experience in manufacturing, with at least 5 years in the medical device or pharma industry.
  • Prior leadership role in managing large-scale, regulated production lines.

Key Competencies

  • In-depth knowledge of regulatory standards (ISO 13485, GMP, FDA, EU MDR).
  • Excellent team leadership, communication, and conflict-resolution skills.
  • Proven track record in implementing continuous improvement and cost-saving initiatives.
  • Hands-on experience with ERP/MES systems.
  • Strong analytical and decision-making abilities.

Why Join Us?

  • Opportunity to lead in a fast-growing, innovation-driven organization
  • Work on cutting-edge medical technologies that impact lives
  • A culture that values quality, teamwork, and continuous learning

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