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.
- Professional and compliance-driven work environment.
Work Location: In person
