Project Details

Consultant - Manufacturing & Quality

An Indian biopharmaceutical company

 Kuala Lumpur

Posted on:  17/12/2021

Cinque Terre

Starts on:  24/12/2021




Manufacturing oversight, Quality assurance, Manufacturing/Operations head, Maintenance,



Company Details

An Indian biopharmaceutical company

Assignment Details

1) Adherence to cGMP (Current Good Manufacturing Practice) and cGLP (Current Good Laboratory Practice). Inspection and testing of incoming material (RM/PM/Consumables) samples
2) Preparation and review of packaging materials specifications, art works, shade cards and generation and maintenance of Quality records.
3) Coordinate with all interphasing departments for Packaging material queries. Preparation of standard operating procedures, instrument/equipment operating procedures, general analytical methods, packaging material specifications.
4) Review of TTD documents, identification and investigation of nonconforming materials. Investigation of OOS results.
5) Maintenance and calibration of measuring and testing equipment belonging to the quality control laboratory in coordination with maintenance department.
6) Issuance of Checklists/log sheets for record entries and nsuring effective implementation of EHS management system in the organization.
7) Reporting of laboratory Incidents, review and Approval of Incoming materials test reports and in SAP.

This is a 6 months project full time onsite in Malaysia.

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


Nature of Work


Profile Requirements

Experience: 10+ years

Qualification : Graduate

fleXpertise required

cGMPPacking materialRaw materialRMPM


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