QA QMS Document Reviewer – Quality Assurance | Ceph Lifesciences | Baddi, Himachal Pradesh, India
Ceph Lifesciences is hiring a QA QMS Document Reviewer in Baddi for its pharmaceutical operations. This role is suitable for candidates with 8–10 years of experience in QMS documentation, QA systems, and compliance.
Location
Baddi, Himachal Pradesh, India
Employment Type
Full-time
Experience Required
8–10 Years
Compensation & Benefits
Not Disclosed
About Ceph Lifesciences
Ceph Lifesciences is a pharmaceutical company focused on high-quality manufacturing and regulatory compliance.
Position Overview
The QA QMS Document Reviewer will manage and review quality documents and ensure compliance with QMS systems.
Key Responsibilities
- Review QMS documentation
- Ensure GMP compliance
- Handle document control processes
- Support audits and inspections
- Maintain QA documentation
- Coordinate with departments
- Monitor quality systems
- Handle deviations and CAPA
- Ensure documentation accuracy
- Follow SOPs
Required Skills & Competencies
- QMS knowledge
- Documentation expertise
- GMP compliance understanding
- Attention to detail
- Communication skills
- Problem-solving ability
- Analytical thinking
- Team coordination
- Compliance knowledge
- Technical aptitude
Educational Qualification
BPharm / MPharm
About the Project & Industry
Quality assurance and QMS systems in pharmaceutical manufacturing.
Why Join Ceph Lifesciences?
Opportunity to work in QA systems and compliance with career growth.
How to Apply
Send your resume to hr.u6@cephlife.com
Check our website — www.ackjobs.com — regularly for the latest updates in the job market. Join our WhatsApp and social media groups from the website.