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:

- Competitive salary package.
- Career growth opportunities.
- Qualified and compliance-driven work environment.

Work Location: In person

📌 Officer / Sr. Officer – QMS Documentation (India)
🏢 Yeble Accelarate your placement
📍 India