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Project Details

Consultant - Process Improvement (In-process team)

An Indian biopharmaceutical company

 Kuala Lumpur, Singapore, Mumbai / Navi Mumbai, Delhi / NCR, Kolkata, Chennai, Bangalore, Pune, Hyderabad

Posted on:  11/09/2019

Cinque Terre

Starts on:  23/09/2019

BROAD CATEGORY

Strategy and Business Development

SUB CATEGORY

Business planning processes, Data analytics,

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 an Analytical consultant to support their team.

Key responsibilities include:
1. Adherence to cGMP (Current Good Manufacturing Practice) and Good Laboratory Practice.
2. Production process control in coordination with production for receipt of Inprocess samples.
3. In process, finished product and stability samples inspection, testing and review of Audit trails for Inprocess analysis.
4. Identification recording and evaluation of all Nonconforming products. Corrective and preventive actions as and where applicable. Preparation, Review and maintenance of Quality Records and Review of product specifications and Analytical reports.
5. Issue and review of log sheets/Annexures/Raw data books/Checklist/log sheets for record times.
6. Handling and Investigation of OOS, OOT, Deviations and Incidents and ensuring effective implementation of EHS management system in the organization.
7. Coordinating with the cross functional teams to address regulatory queries. Maintaining team co-ordination and communicate relevant EHS issues to concerned personnel.

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

Skills Required

Work Experience in Analytical OOS, OOT
Experience in working and implementation of EHS management
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: 12+ years

Qualification: Post Graduate or Higher

fleXpertise required

AnalyticalOOS OOTcGMPInprocess

ESTIMATED BUDGET (Monthly)

-

 

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