QC Analyst Jobs in Helios Pharmaceuticals - Baddi, Himachal Pradesh

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QC Analyst Jobs in Helios Pharmaceuticals - Baddi, Himachal Pradesh

work outline icon2 - 4 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Helios Pharmaceuticals

time outline iconBaddi, Himachal Pradesh, India

Posted on 27-04-2026

2 Vacancies

Description

  • Job Title: QC Analyst
  • Qualification: BPharm/MPharm
  • Location: Helios Pharmaceuticals - Baddi, Himachal Pradesh
  • Work Experience: 2 to 4 Years

Job Description

  • Perform analysis of raw materials, in-process samples, and finished products.
  • Operate analytical instruments such as HPLC, GC, UV, and dissolution apparatus.
  • Prepare reagents, solutions, and standardize volumetric solutions.
  • Record and maintain analytical data, test reports, and documentation.
  • Follow GLP, GMP, and laboratory safety guidelines.
  • Conduct calibration and routine maintenance of laboratory instruments.
  • Handle OOS (Out of Specification) and OOT (Out of Trend) investigations.

Take this opportunity to join Helios Pharmaceuticals - Baddi, Himachal Pradesh as a QC Analyst 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

MPharm (Master Of Pharmacy)BPharm (Bachelor Of Pharmacy)

Key Skills

Problem Solving SkillsAnalytical SkillsDocumentationAttention to Detail

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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