QA Officer Jobs in CEPH Lifesciences Private Limited - Haridwar, Uttarakhand

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QA Officer Jobs in CEPH Lifesciences Private Limited - Haridwar, Uttarakhand

work outline icon0 - 4 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

CEPH Lifesciences Private Limited

time outline iconHaridwar, Uttarakhand, India

Posted on 07-04-2026

1 Vacancy

Description

  • Job Title: QA Officer
  • Qualification: BPharm
  • Location: CEPH Lifesciences Private Limited - Haridwar, Uttarakhand
  • Work Experience: 0 to 4 Years

Job Description

  • Ensure compliance with GMP and quality assurance standards.
  • Review batch manufacturing records and quality documents.
  • Monitor production processes for quality compliance.
  • Handle deviations, CAPA, and change control documentation.
  • Conduct internal audits and quality inspections.
  • Coordinate with QC and production teams for quality issues.
  • Maintain QA documentation and quality records.
  • Support regulatory audits and quality improvement activities.

Take this opportunity to join CEPH Lifesciences Private Limited - Haridwar, Uttarakhand as a QA Officer in Haridwar, Uttarakhand 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 Assurance (QA)

Preferred Education

BPharm (Bachelor Of Pharmacy)

Key Skills

DocumentationProblem Solving SkillsCoordination SkillsAttention to Detail

About Organization

CEPH Lifesciences Private Limited is a pharmaceutical organization engaged in the manufacturing of high-quality formulations with a strong focus on regulatory compliance, product quality, and efficient production processes. The role involves working in a manufacturing or operational environment to support production activities and ensure adherence to industry standards. Responsibilities include assisting in production operations, following Good Manufacturing Practices (GMP), maintaining accurate batch records and documentation, monitoring equipment performance, and ensuring compliance with safety and hygiene protocols. The role also requires coordination with quality assurance and quality control teams, adherence to regulatory guidelines, and maintaining consistency in product quality and operational efficiency.

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