A leading pharmaceutical manufacturing facility in Baddi, Himachal Pradesh, is hiring a Junior Team Member – QC (Quality Control). This opportunity is ideal for M.Sc. or B.Pharm graduates with 1–3 years of QC experience and strong knowledge of pharmacopoeial updates, SOP preparation, and cGMP compliance.
Baddi is one of India’s largest pharmaceutical manufacturing hubs, making this QC job in Himachal Pradesh a strategic career move for professionals seeking regulatory exposure and documentation expertise.
🔎 Job Overview
- Position: Junior Team Member – QC
- Location: Baddi, Himachal Pradesh, India
- Experience: 1–3 years in QC department
- Qualification: M.Sc. / B.Pharm
- Department: Quality Control (Documentation & Compliance)
This QC pharmaceutical job in Baddi focuses on documentation management, pharmacopoeial compliance, and harmonization of analytical procedures across units.
📌 Key Responsibilities
1️⃣ SOP & Documentation Management
- Prepare and revise SOPs, specifications, and analytical methods
- Update corporate QC documents in coordination with QA/QC
- Review instrument calibration data as per operating documents
- Ensure GMP-compliant documentation on digital systems (e.g., CipDox)
2️⃣ Pharmacopoeial Compliance & Updates
- Review latest pharmacopoeial amendments and monographs
- Monitor timely implementation before effective dates
- Escalate non-conformances to avoid regulatory risk
- Coordinate with regulatory teams for compliance alignment
3️⃣ Digital & System Documentation
- Maintain accurate online entries using approved formats
- Ensure deviation documentation and system integrity
- Update and issue controlled documents & bound books
4️⃣ Process Harmonization
- Standardize documentation across multiple units
- Work with Cross Functional Teams (CFTs)
- Identify simplification opportunities to improve workflow efficiency
🎯 Key Performance Indicators (KPIs)
- Support 4 units for documentation updates
- Handle ~10 documentation reviews/preparations per month
- Finalize ≥80% documents within timeline
- Ensure 100% pharmacopoeial update implementation
🎓 Eligibility Criteria
- Educational Qualification: M.Sc. or B.Pharm
- Experience: 1–3 years in pharmaceutical QC
- Strong knowledge of:
- cGMP & regulatory standards
- Pharmacopoeia (IP, USP, BP, EP updates)
- SOP drafting & document control systems
- Quality compliance norms
💼 Why This QC Job in Baddi is a Good Career Move
- Exposure to regulatory documentation & compliance
- Hands-on involvement in pharmacopoeial implementation
- Opportunity to work across multiple units
- Strong foundation for future roles in:
- QA Documentation
- Regulatory Affairs
- Quality Systems Management
📍 Location Advantage – Baddi Pharma Hub
Baddi, Himachal Pradesh, is home to major pharmaceutical manufacturing plants and offers long-term career growth in QC, QA, and Regulatory Affairs roles.
📩 How to Apply
