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Project Details

Consultant - Manufacturing & Quality

An Indian biopharmaceutical company

 Mumbai / Navi Mumbai, Delhi / NCR, Kolkata, Chennai, Bangalore, Pune, Hyderabad

Posted on:  11/03/2022

Cinque Terre

Starts on:  21/03/2022

BROAD CATEGORY

Manufacturing/Operations

SUB CATEGORY

Manufacturing oversight, Quality assurance, Manufacturing/Operations head, Process Engineering / Process excellence,

INDUSTRY

Pharmaceuticals

Company Details

An Indian biopharmaceutical company manufacturing generic active pharmaceutical ingredients that are sold in over 120 countries across the globe

Assignment Details

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

Skills Required

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

Assignment Duration

6 month(s)

Capacity Required

Full Time

No. of Positions

1

Nature of Work

On-Site

Profile Requirements

Experience: 8+ years

Qualification : Graduate

fleXpertise required

qualitypharma CFTs.documentation Manufacturing

ESTIMATED BUDGET (Total Budget)

-

 

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