1 years

14 - 16 Lacs

Posted:2 days ago| Platform: GlassDoor logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Key Responsibilities :- Male Candidate Required From Maharashtra Location

  • Strategy & Systems: Develop and implement quality systems (QMS) aligned with GMP, GLP, and regulatory norms (FDA, CDSCO).
  • Leadership: Lead, train, and mentor QA/QC teams, setting department objectives and managing budgets.
  • Operations Oversight: Supervise testing of raw materials, in-process, and finished products; manage documentation, validations, and change controls.
  • Compliance & Audits: Ensure adherence to regulations, prepare for audits, and manage internal/external inspection readiness.
  • Problem Solving: Investigate quality issues, implement Corrective & Preventive Actions (CAPAs), and drive continuous improvement.
  • Cross-functional Collaboration: Work with R&D, Production, and Regulatory teams to integrate quality into all processes.
  • Reporting: Prepare quality reports and present quality performance to senior management.
  • Revised schedule M :- Need to implement inline in factory departments within 1 year
  • Smart and excellent skill person required who tackle all difficult situations

Essential Skills & Qualifications

  • Education: B.Pharm/M.Pharm, Life Sciences/M.Sc. B.Sc.Chemistry background.
  • Experience: 17 to 20 years of experience
  • Technical: Deep knowledge of GMP, GLP, validation, analytical techniques (HPLC, GC).
  • Soft Skills: Strong leadership, problem-solving, analytical, communication, and attention to detail.

Job Types: Full-time, Permanent

Pay: ₹1,400,000.00 - ₹1,600,000.00 per year

Benefits:

  • Health insurance
  • Leave encashment
  • Provident Fund

Work Location: In person

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