Junior Team Member - QC
Company: Pharmaceutical Organization
Location: Rangpo
Job Type: Full-Time
Experience: 1–3 Years
Qualification: M.Sc. / B.Pharm
Job Overview
This role focuses on quality control documentation and compliance within a pharmaceutical environment. The position involves preparing, reviewing, and maintaining SOPs, specifications, and regulatory documents to ensure alignment with pharmacopoeial standards and cGMP requirements.
Key Responsibilities
Documentation & SOP Management
Prepare, update, and review SOPs, specifications, and analytical documents
Ensure documents are aligned with pharmacopoeia and regulatory standards
Support QC/QA teams with required documentation
Regulatory & Pharmacopoeia Compliance
Review pharmacopoeial updates and implement required changes
Ensure compliance with latest guidelines and standards
Coordinate with regulatory teams for approvals and updates
Data & Record Management
Maintain accurate and compliant documentation records
Ensure proper entries in systems like CipDox
Handle deviations and ensure data integrity
Document Control & Distribution
Issue and track controlled documents and bound books
Maintain logs and ensure latest versions are available
Ensure proper documentation flow across departments
Process Improvement
Support harmonization and simplification of documents
Collaborate with cross-functional teams to improve processes
Suggest improvements for efficiency and standardization
Required Skills
Knowledge of cGMP and pharmacopoeial standards
Strong documentation and compliance understanding
Attention to detail and accuracy
Coordination with cross-functional teams
Time management and ability to meet deadlines
Why This Role Matters
This position ensures that all QC documentation and processes meet strict regulatory and quality standards, directly impacting product quality and compliance in pharmaceutical manufacturing.
Uttar Pradesh :
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Canada |Quebec :
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Japan | Saitama |Tokyo :
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