company-details

QA Executive

MBA/BBA

9 hours ago

Job Description

Manage documentation, Quality Management Systems (QMS), and validation activities in a pharmaceutical manufacturing setup. Ensure compliance with regulatory standards and support audits and continuous improvement. This is a full-time, in-person role based in Baddi.



Key Responsibilities

Handle documentation related to manufacturing and compliance.

Implement and maintain Quality Management Systems (QMS) as per regulatory requirements.

Coordinate and execute validation activities (process validation, equipment qualification, cleaning validation, etc.).

Ensure adherence to standard operating procedures and maintain proper records for audits and inspections.

Support internal audits and continuous improvement initiatives.

Skill & Experience
  • manufacturing
  • Quality Assurance
  • Quality control
  • Functional testing
Job Overview

Date Posted:

4th Jul, 2025

Expiration date:

24th Jul, 2026

Location:

Baddi , Himachal Pradesh, India

Job Type:

Full-time

Functional Areas:

Documentation Control

Positions:

1

Job Experience:

0 Year

Salary Period:

Monthly Pay Period

Is Freelance:

No

Job Skills
  • manufacturing
  • Quality Assurance
  • Quality control
  • Functional testing
Company Overview
company-details

Nootan Pharmaceuticals

View company profile

Founded in:

2010

Location:

Village Tipra, Barotiwala‑Kalka Road (Barotiwala), Tehsil Baddi, District Solan, HP – 174103

Open Jobs : 1