Technical Supervisor-QC (FP) Jobs in Cadila Pharmaceuticals Ltd - Ahmedabad, Gujarat

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Technical Supervisor-QC (FP) Jobs in Cadila Pharmaceuticals Ltd - Ahmedabad, Gujarat

work outline icon0 - 2 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Cadila Pharmaceuticals Ltd

time outline iconAhmedabad, Gujarat, India

Posted on 25-06-2026

1 Vacancy

Description

  • Job Title: Technical Supervisor-QC (FP)
  • Qualification: BSc Chemistry
  • Location: Cadila Pharmaceuticals Ltd - Ahmedabad, Gujarat
  • Work Experience: 0 to 2 Years

Job Description

  • Supervise daily maintenance activities of plant machinery, equipment, and utility systems.
  • Ensure preventive and corrective maintenance of mechanical, electrical, and instrumentation systems.
  • Monitor machine performance and identify faults to reduce breakdowns and downtime.
  • Coordinate with production team to ensure smooth workflow without interruptions.
  • Maintain maintenance logs, service reports, and equipment history records.
  • Manage spare parts inventory and coordinate procurement when required.

Take this opportunity to join Cadila Pharmaceuticals Ltd - Ahmedabad, Gujarat as a Technical Supervisor-QC (FP) in Ahmedabad, Gujarat and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.

Category

Engineering / Maintenance

Preferred Education

BSc Chemistry

Key Skills

Time Management SkillTroubleshootingProblem SolvingTeam Supervision

About Organization

Cadila Pharmaceuticals Ltd is a leading pharmaceutical company engaged in the manufacturing, research, and development of high-quality medicines and healthcare products. The company operates advanced production facilities and follows strict regulatory and quality standards. The role involves supporting production activities and ensuring smooth manufacturing operations in the plant. Responsibilities include operating equipment, monitoring processes, and maintaining batch records while following SOP and GMP guidelines. The position focuses on efficient production, product quality, and adherence to pharmaceutical manufacturing standards

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