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PACKAGING COORDINATOR

Employment Type Permanent
Location Hampshire , Hampshire
Industry Sector Manufacturing
Start Date asap
Salary/Rate ŁNeg + Benefits
Reference TP575
Date Advertised 04-09-2008 - 12:26

This vacancy is out of date and no longer accepting applications.

Description

Our Client manufactures, packages and redistributes a range of OTC pharmaceuticals, distributed world-wide. They have the requirement for a Packaging Coordinator to ensure efficient project coordination and change implementation regarding new packaging introduction and changes to current packaging, according to Customer requirements. This role will encompass Quality Control, Quality Assurance, and Customer / Department liaison.

Our Client manufactures, packages and redistributes a range of OTC pharmaceuticals, distributed world-wide. They have the requirement for a Packaging Coordinator to ensure efficient project coordination and change implementation regarding new packaging introduction and changes to current packaging, according to Customer requirements. This role will encompass Quality Control, Quality Assurance, and Customer / Department liaison. Candidates should have project coordination experience, with knowledge of Quality Assurance and Quality activities surrounding new packaging introduction.

Job Summary

To Control and Coordinate Packaging Change activities across all areas of the business, and support site initiatives
To ensure that relevant quality systems operate effectively across the organisation, suggesting and facilitating opportunities for improvement
To generate and or review documentation as appropriate
To ensure that all associated investigations are performed effectively and efficiently, true root cause is identified and that all corrective actions are tracked to completion
To provide Technical Support across the organisation and where appropriate, inspection management & audit support
Where appropriate to provide sampling and testing of incoming materials

Training, Education and Experience

Educated to HNC or equivalent, preferably in Pharmaceutical / Scientific discipline
Knowledge of cGMP and its implementation by Regulatory Authorities
Knowledge of corporate quality systems
Excellent written and oral communication skills, able to liaise with and influence people on all levels of the organisation