Sr. Officer-Quality Control Jobs in Meril Life Sciences Private Limited - Vapi, Gujarat

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Sr. Officer-Quality Control Jobs in Meril Life Sciences Private Limited - Vapi, Gujarat

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

Meril Life Sciences Private Limited

time outline iconVapi, Gujarat, India

Posted on 02-02-2026

1 Vacancy

Description

  1. Job Title: Sr. Officer-Quality Control
  2. Qualification: Bsc/Msc
  3. Location: Meril Life Sciences Private Limited - Vapi, Gujarat
  4. Work Experience: 2 to 4 Years

Job Description

  1. Perform QC analysis of raw materials, in-process, and finished products.
  2. Operate and maintain analytical instruments as per SOPs.
  3. Ensure compliance with GMP, GLP, and regulatory guidelines.
  4. Prepare, review, and maintain QC documentation and records.
  5. Investigate OOS/OOT results and support CAPA activities.
  6. Support stability studies and sample analysis.
  7. Participate in method validation/transfer activities.
  8. Ensure proper calibration and maintenance of lab instruments.
  9. Assist during internal, customer, and regulatory audits.
  10. Train junior staff and support continuous improvement initiatives.

Take this opportunity to join Meril Life Sciences Private Limited - Vapi, Gujarat as a Sr. Officer-Quality Control in Vapi, 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 Control (QC)

Preferred Education

BSc ChemistryMSc Chemistry

Key Skills

DocumentationAnalytical SkillsSample ManagementProblem Solving Skills

About Organization

Meril Life Sciences Private Limited, Vapi, Gujarat, is a leading medical device and healthcare company known for its strong quality systems, regulatory compliance, and innovation-driven manufacturing environment. The company invites applications for Sr. Officer – Quality Control positions to perform and oversee quality control testing, review and approval of analytical data, ensure compliance with GMP/ISO standards, support method validation and stability studies, handle OOS/OOT investigations, maintain laboratory documentation, and coordinate with QA, production, and regulatory teams. This role offers exposure to a regulated medical device manufacturing setup, opportunities for technical growth, and long-term career development in a quality-focused organization.

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