Qualification: B.Sc. / B.Pharma

Location: Dehradun, Roorkee, Haridwar

Job Description:

We are seeking a proactive and organized QMS Documentation Officer / Sr. Officer to support and maintain Quality Management System documentation in a pharmaceutical manufacturing environment. The candidate will be responsible for controlling quality documents, ensuring regulatory compliance, and supporting continuous quality improvement initiatives.

Key Responsibilities:
Prepare, review, issue, and archive controlled quality documents.
Maintain SOPs, specifications, formats, protocols, and records as per QMS requirements.
Coordinate document revisions and ensure timely implementation.
Track document lifecycle activities and maintain document control logs.
Support internal audits and regulatory inspections by providing required documentation.
Ensure compliance with GMP,



GDP, and company quality standards.
Assist in handling deviations, CAPA, change controls, and risk assessment documentation.
Maintain proper filing and retrieval systems for quality records.

Required Skills:
Strong knowledge of pharmaceutical documentation practices.
Familiarity with GMP, GDP, and QMS requirements.
Good attention to detail and organizational skills.
Proficiency in MS Office applications.

Eligibility:
B.Sc. or B.Pharma qualification.

Benefits:
Market-competitive salary package.
Growth opportunities opportunities.
Professional and compliance-driven work workplace.

Work Location: In person

📌 Officer / Sr Officer – Qms Documentation Selakui
🏢 Yeble Accelarate your placement
📍 Selakui