Executive/Sr. Executive-QA (QMS) Jobs in Verve Human Care Laboratories - Ahmedabad, Gujarat

Executive/Sr. Executive-QA (QMS) Jobs in Verve Human Care Laboratories - Ahmedabad, Gujarat

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

Verve Human Care Laboratories

time outline iconAhmedabad, Gujarat, India

Posted on 03-07-2026

1 Vacancy

Description

  • Job Title: Executive/Sr. Executive-QA (QMS)
  • Qualification: BPharm
  • Location: Verve Human Care Laboratories - Ahmedabad, Gujarat
  • Work Experience: 10 to 15 Years

Job Description

  • Plan, execute, and document validation activities including IQ, OQ, and PQ.
  • Perform process validation, cleaning validation, and equipment qualification.
  • Prepare and review validation protocols, reports, and SOPs.
  • Ensure compliance with GMP, GLP, and regulatory requirements.
  • Coordinate with production, QC, and engineering teams for validation activities.
  • Handle revalidation, change control, and risk assessment (QRM).
  • Monitor validation schedules and ensure timely completion.

Take this opportunity to join Verve Human Care Laboratories - Ahmedabad, Gujarat as a Executive/Sr. Executive-QA (QMS) in Ahmedabad, Gujarat 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

Attention to DetailProblem SolvingRisk AssessmentDocumentation

About Organization

Verve Human Care Laboratories is a pharmaceutical company focused on developing, manufacturing, and marketing high-quality pharmaceutical formulations and healthcare products with an emphasis on innovation, regulatory compliance, and quality standards. The role involves working in a professional pharmaceutical environment to support production, quality assurance, quality control, 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 smooth business operations. The role also requires strong analytical skills, teamwork, adherence to regulatory guidelines, and commitment to delivering safe, effective, and high-quality pharmaceutical products and healthcare solutions.

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