Sr. Executive-IPQA (Injection) Jobs in Beta Drugs Ltd - Baddi, Himachal Pradesh

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Sr. Executive-IPQA (Injection) Jobs in Beta Drugs Ltd - Baddi, Himachal Pradesh

work outline icon6 - 8 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Beta Drugs Ltd

time outline iconBaddi, Himachal Pradesh, India

Posted on 19-06-2026

1 Vacancy

Description

  • Job Title: Sr. Executive-IPQA (Injection)
  • Qualification: BPharm
  • Location: Beta Drugs Ltd - Baddi, Himachal Pradesh
  • Work Experience: 6 to 8 Years

Job Description

  • Perform in-process quality checks during manufacturing and packing operations.
  • Ensure compliance with GMP, SOPs, and quality standards on the shop floor.
  • Monitor critical process parameters and ensure adherence to validated processes.
  • Review batch manufacturing and packing records for accuracy and completeness.
  • Report deviations, non-conformances, and support root cause investigations.
  • Verify line clearance activities before and after each batch/shift.
  • Ensure proper documentation and real-time recording of in-process activities.

Take this opportunity to join Beta Drugs Ltd - Baddi, Himachal Pradesh as a Sr. Executive-IPQA (Injection) in Baddi, Himachal Pradesh 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 IPQA

Preferred Education

BPharm (Bachelor Of Pharmacy)

Key Skills

Time Management SkillAttention to DetailTeam working SkillsProblem Solving Skills

About Organization

Beta Drugs Ltd is a pharmaceutical manufacturing company focused on developing, manufacturing, and marketing high-quality oncology formulations and 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, documentation, and operational activities. Responsibilities include maintaining GMP compliance, handling manufacturing and quality records, coordinating with cross-functional teams, monitoring production 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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