Overview
We are searching for the best talent for the Quality Control Scientist position to be in Blackpool, UK.
Purpose
To carry out QC testing to ensure the ongoing quality of product and to interface with other Departments to ensure the timely approval of products. To ensure that the principles of cGMP are applied and that all documentation, in the form of procedures and specifications, is followed to guarantee compliance with ISO 13485, FDA QMSRs and the global Medical Device regulations and standards.
Responsibilities
* Ensure that all routine QC testing is performed in a timely manner in line with agreed schedules.
* Perform physical testing of raw material, in process and finished product.
* Perform analytical testing of raw material, in process and finished goods.
* Perform chemical testing of raw material, in process and finished goods.
* Perform maintenance of standards and reagents.
* Be responsible for management of consumables and materials used in testing.
* Ensure all lab equipment is working/calibrated/validation and to arrange for repairs/call out engineers as required to coordinate safety issues within the laboratory environment.
* Ensure all documentation and testing is completed on time to ensure timely release to customers both internal and external.
* Liaise with external testing organizations or test houses to ensure product data is retrieved and available in a timely manner.
* Ensure purchase orders are raised in a timely manner to limit stock outs.
Qualifications / Requirements
* BSc or in a relevant Scientific discipline or equivalent; typically 5 year experience within a Quality/Laboratory role in the Food, Medical or Health Care industry.
* Minimum of 3 year Quality laboratory experience within a senior role.
* Good understanding of Quality testing, Analytical instruments and Validation.
Required Knowledge And Skills
* Implement improvements to working practices.
* Ability to communicate & present (in all its forms) and cooperate effectively at all levels across the organisation.
* An attention to detail.
* Ability to prioritise own work and to work to deadlines.
* Ability to cope under pressure and to react to changing requirements.
* Ability to work effectively as part of a team to achieve results.
* Ability to manage their own time and workload and to work independently using own initiative (Excellent time-management).
* Computer literacy – specifically use of E-mail and MS Office software.
* To ensure that the principles of cGMP are applied and that all documentation, in the form of procedures and specifications, is followed to guarantee compliance with ISO 13485, FDA QMSRs and global Medical Device regulations and standards.
* Customer Focus: Results & Performance Driven & Sense of Urgency.
* Innovative Solutions: Big Picture Orientation with Attention to Detail & Intellectual Curiosity.
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