Quality Engineer x 3 - CONTRACT

Midlands  ‐ Onsite
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Description

Quality Engineer x 3 - Pharmaceutical/Medical Device - CONTRACT

Location: East Midlands, UK

Duration: Initially 6 months - Very likely long term extensions beyond

My exclusive global client urgently requires the services of 3 x Contract Quality Engineers to join a new project team taking responsibility of supporting internal customer complaint data acquisition, root cause analysis and draft complaint responses. These roles will also support the Quality Manager in the provision of support for product and process improvements by collecting, compiling and analysing data. Furthermore, these roles will support continuous improvement projects relating to both sustaining engineering and product development activities.

Main Duties:
* Ensuring effective investigations related to site discrepancies and customer complaints.
* Ensuring interface with corporate complaints group for execution of customer complaints.
* Provide trend analysis reports related to customer complaints and CAPA.
* Work independently with project teams to develop control deliverables including quality plans, manufacturing & inspection documentation, test methods, and any necessary records for compiling history file.
* Participate in the development and maintenance of product risk hazard analysis.
* Meet company and departmental goals in the continuous improvement of all products, services and processes.
* Support quality assurance improvement activities by evaluating products, processes or materials in order to develop control or improvement strategies intended to improve the customer's experience.
* Work with management and technical staff in performing root cause failure analysis and implementing corrective and preventative actions to preclude recurrence.
* Support both corporate and facility driven initiatives intended to meet defined objectives.

Qualifications and Person Specification:
* Minimum BS/BA in engineering or Science.
* Minimum of 2 years experience in pharmaceutical or medical device manufacturing environment
* Knowledge of ISO 9001:2008, ISO 13485, 21 CFR 820, 21 CFR 210 & 211, cGMP, cGLP
* Ability to work independently and in a team environment
* Demonstrate innovativeness in tactical matters relating to proposing alternate solutions for process improvement
* Must possess or be willing to develop:
* Problem solving skills, preferably experience Lean and Six Sigma
* Effective presentation/communication skills, both oral and written, project/resource management skills
* Ability to manage multiple projects in a fast-paced environment

CPS Group (UK) Ltd is acting as an Employment Business in relation to this vacancy.

Start date
ASAP
Duration
6months +
(extension possible)
From
CPS Group (UK) Ltd
Published at
15.07.2014
Project ID:
742001
Contract type
Freelance
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