QC Executive (GLP) Jobs in Helios Pharmaceuticals - Baddi, Himachal Pradesh

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QC Executive (GLP) Jobs in Helios Pharmaceuticals - Baddi, Himachal Pradesh

work outline icon3 - 5 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Helios Pharmaceuticals

time outline iconBaddi, Himachal Pradesh, India

Posted on 27-04-2026

1 Vacancy

Description

  • Job Title: QC Executive (GLP)
  • Qualification: BPharm (Bachelor Of Pharmacy)
  • Location: Helios Pharmaceuticals - Baddi, Himachal Pradesh
  • Work Experience: 3 to 5 Years

Job Description

  • Perform routine analysis of raw materials, packaging materials, in-process, and finished products as per specifications.
  • Conduct testing using instruments such as HPLC, UV Spectrophotometer, FTIR, Dissolution apparatus, and other QC equipment.
  • Record and maintain analytical data accurately in laboratory notebooks and electronic systems.
  • Ensure compliance with GMP, GLP, and data integrity guidelines during all QC activities.

Take this opportunity to join Helios Pharmaceuticals - Baddi, Himachal Pradesh as a QC Executive (GLP) 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 Quality Control (QC)

Preferred Education

BPharm (Bachelor Of Pharmacy)

Key Skills

Communication SkillsAttention to DetailDocumentationTeam Coordination

About Organization

Helios Pharmaceuticals is a pharmaceutical manufacturing organization focused on delivering high-quality healthcare products with a strong emphasis on quality assurance, regulatory compliance, and efficient production processes. The role involves working in a pharmaceutical manufacturing setup to support production activities and ensure smooth functioning of operations. Responsibilities include assisting in manufacturing processes, coordinating with quality control and quality assurance teams, maintaining accurate batch records and documentation, and following standard operating procedures (SOPs). The role focuses on maintaining product quality, ensuring compliance, and supporting seamless manufacturing operations while upholding high standards of pharmaceutical production.

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