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

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Technical Assistant-Packing (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-Packing (OSD)
  • Qualification: BPharm (Bachelor Of Pharmacy)
  • Location: Aurobindo Pharma Limited - Jadcherla, Telangana
  • Work Experience: 0 to 5 Years

Job Description

  • Responsible for packing finished products as per approved packing standards and SOPs.
  • Ensure correct labeling, coding, and sealing of packed materials.
  • Perform visual inspection to identify defects or damages before packing.
  • Maintain cleanliness and hygiene in the packing area as per GMP guidelines.
  • Operate packing machines and tools safely and efficiently.
  • Follow batch records, packing instructions, and quality requirements.

Take this opportunity to join Aurobindo Pharma Limited - Jadcherla, Telangana as a Technical Assistant-Packing (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

Pharma Labeling & Packaging

Preferred Education

BPharm (Bachelor Of Pharmacy)

Key Skills

Good CommunicationTeam working SkillsAttention to DetailDecision Making

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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