Asst. Manager-QA Jobs in Naari Pharma Private Limited - Rudrapur, Uttrakhand

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Asst. Manager-QA Jobs in Naari Pharma Private Limited - Rudrapur, Uttrakhand

work outline icon3 - 10 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Naari Pharma Private Limited

time outline iconRudrapur, Uttarakhand, India

Posted on 02-02-2026

1 Vacancy

Description

Job Requirements

  1. Job Title: Asst. Manager-QA
  2. Location: Naari Pharma Private Limited - Rudrapur, Uttrakhand
  3. Qualification: Master of Science
  4. Work Experience: 3 to 10 Years

Job Description

  1. Ensure compliance with cGMP, ISO, and regulatory standards in all QA operations.
  2. Review and approve batch records, SOPs, protocols, and quality documentation.
  3. Investigate deviations, complaints, and non-conformances; implement corrective and preventive actions (CAPA).
  4. Conduct internal audits and support external inspections by regulatory authorities.
  5. Coordinate with Production, R&D, QC, and Regulatory teams for quality compliance.

Take this opportunity to join Naari Pharma Private Limited - Rudrapur, Uttrakhand as a Asst. Manager-QA in Rudrapur, Uttrakhand 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

MSc (Master of Science)

Key Skills

Analytical SkillsTeam ManagementInterpersonal skillsProblem Solving

About Organization

Naari Pharma Private Limited is an Indian pharmaceutical manufacturing company engaged in the production of Active Pharmaceutical Ingredients (APIs), bulk drugs, and intermediates. The company focuses on supplying high-quality pharmaceutical raw materials to formulation manufacturers in India and international markets. Operates within a SIDCUL-approved industrial area with regulatory approvals from the Uttarakhand State Pollution Control Board. Manufacturing facilities are designed for large-scale production of intermediates and bulk drugs. Emphasis on quality compliance, regulated manufacturing processes, and export-oriented production.

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