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Our client is looking to engage with a consultant who has experience in pharma QC experience with good documentation skills.
1. Adherence to Quality Policies, EHS policies, cGMP (Current Good Manufacturing
Practice), cGLP (Current Good Laboratory Practice)
2. Evaluation of all raw material, Packaging material and Consumable specifications,
Identify the gaps in specifications and address the same through appropriate justification
and impact assessment in co-ordination with CFTs.
3. Training on the updated procedures as and when required.
4. Preparation / Review of documents
5. Evaluation of Pharmacopeia and In-House test methods and their alignment with testing
specification / standard Testing Procedures.
6. Preparation and Review of specifications and worksheets
Please note: onsite - Bangalore
Work Experience in RMPM would be preferred
Experience in working and implementation of WMS -ERP systems necessary
Experience and working in mechanized and sophisticated material handling preferred
High proficiency in Microsoft Office
Excellent Communication and interpersonal skills required
An Indian biopharmaceutical company manufacturing generic active pharmaceutical ingredients that are sold in over 120 countries across the globe
Pharmaceuticals
8+ years
1
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