Technical Assistant-Production (OSD) Jobs in Aurobindo Pharma Limited - Jadcherla, Telangana

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Technical Assistant-Production (OSD) Jobs in Aurobindo Pharma Limited - Jadcherla, Telangana

work outline icon0 - 5 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Aurobindo Pharma Limited

time outline iconJadcherla, Telangana, India

Posted on 01-06-2026

1 Vacancy

Description

  • Job Title: Technical Assistant-Production (OSD)
  • Qualification: Diploma
  • Location: Aurobindo Pharma Limited - Jadcherla, Telangana
  • Work Experience: 0 to 5 Years

Job Description

  • Oversee production activities to ensure timely completion of batches as per plan.
  • Monitor machine operations and ensure adherence to SOPs and GMP guidelines.
  • Supervise operators, allocate work, and ensure target output and quality.
  • Review batch manufacturing records and maintain production documentation.
  • Conduct in-process checks to ensure product quality and process consistency.
  • Coordinate with QA, QC, maintenance, and warehouse teams for smooth operations.
  • Ensure proper handling of raw materials, equipment, and production lines.Diploma

Take this opportunity to join Aurobindo Pharma Limited - Jadcherla, Telangana as a Technical Assistant-Production (OSD) in Jadcherla, Telangana and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.

Category

Pharmaceuticals

Functional Area

Production / Manufacturing

Preferred Education

Diploma

Key Skills

Good Communication SkillsProblem Solving SkillsDecision-Making SkillsAttention to Detail

About Organization

Aurobindo Pharma Limited is a leading pharmaceutical manufacturing company focused on developing, manufacturing, and marketing high-quality generic medicines, active pharmaceutical ingredients (APIs), and specialty healthcare products with an emphasis on innovation, regulatory compliance, and global quality standards. The role involves working in a professional pharmaceutical manufacturing environment to support production, quality assurance, quality control, research and development, regulatory affairs, supply chain, and operational activities. Responsibilities include maintaining GMP compliance, handling technical and quality documentation, coordinating with cross-functional teams, monitoring manufacturing and quality processes, and supporting efficient plant operations. The role also requires strong analytical skills, teamwork, adherence to regulatory guidelines, and commitment to delivering safe, effective, and high-quality pharmaceutical products.

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