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Raw Material Reviewer

Eurocrit Labs International

Baddi, Solan, Himachal Pradesh

Department: Quality Control

Experience: 2-7 Years

Industry: Pharmaceutical

Education: BSc

Job Description

4692 – Raw Material Reviewer – Quality Control | Eurocrit Labs International | Baddi, Solan, Himachal Pradesh, India

Eurocrit Labs International is hiring a Raw Material Reviewer in Baddi, Solan, Himachal Pradesh, India within the pharmaceutical industry. This role is ideal for professionals with 2–7 years of experience in quality control, raw material analysis, and documentation review. The position involves ensuring that all incoming raw materials meet quality standards and regulatory requirements. Candidates will be responsible for reviewing analytical reports, maintaining compliance with GMP guidelines, and supporting audit readiness. This opportunity provides exposure to pharmaceutical quality systems and regulatory processes, making it suitable for candidates looking to grow in quality control functions.

Location

Baddi, Solan, Himachal Pradesh, India

Employment Type

Full-time (Direct Hiring)

Experience Required

2–7 Years

Compensation & Benefits

Not Disclosed

About Eurocrit Labs International

Eurocrit Labs International is a pharmaceutical company focused on quality testing, analytical services, and regulatory compliance.

Position Overview

The Raw Material Reviewer will be responsible for reviewing raw material test reports and ensuring compliance with quality standards.

Key Responsibilities

  • Review analytical data of raw materials
  • Ensure compliance with GMP and regulatory standards
  • Approve or reject raw materials based on specifications
  • Maintain documentation and audit records
  • Coordinate with QC and QA teams
  • Support regulatory inspections and audits
  • Identify deviations and assist in investigations
  • Ensure adherence to SOPs
  • Maintain data integrity and accuracy
  • Assist in continuous improvement initiatives

Required Skills & Competencies

  • Strong knowledge of QC and raw material analysis
  • Understanding of GMP guidelines
  • Experience in documentation review
  • Analytical and problem-solving skills
  • Attention to detail
  • Regulatory compliance knowledge
  • Team coordination skills
  • Time management
  • Audit readiness experience
  • Communication skills

Educational Qualification

B.Sc

About the Project & Industry

This role operates within the pharmaceutical quality control domain focusing on raw material compliance and testing.

Why Join Eurocrit Labs International?

  • Work in a regulated pharma environment
  • Exposure to quality systems and audits
  • Career growth in QC roles
  • Professional work culture

How to Apply

Send your resume to: hr@eurocrit.com

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