Process Quality Specialist, NPI
|Job Title:||Process Quality Specialist, NPI|
|Contact Name:||Larry O’Leary|
|Job Published:||about 3 years ago|
Our client, a blue-chip multinational company, now seek an experienced Process Quality Specialist to project manage the transition of new products from R&D sister site into commercial manufacture. This is a permanent role based in Cork.
The successful candidate will overseeing all issues within manufacturing on existing products & new product from development and associated tech transfers, within an FDA regulated environment.
Responsibilities of Process Quality Specialist, NPI:
Manage customer complaints, process validations, regulatory documentation, perform internal quality audits.
Lead transfer and implement product and processes from development or from another manufacturing facility.
Project manages a number of QA projects in line with the implementation of Lean Manufacturing programme across the site.
Implement and drive process improvements to ensure predictable processes across all product lines.
Provide effective and responsive QA support to Operations to meet their KPIs.
Implement and drive and implement plant wide quality system improvements.
Identification and implementation of appropriate statistical techniques to monitor process performance.
Approval of change requests for product, process and quality system changes.
Ensure Regulatory compliance in area of responsibility to cGMP's.
Requirements for Process Quality Specialist, NPI:
Honours Bachelor's Degree in Science, Engineering, or equivalent.
4+ years Quality experience in GMP environment, of which at least 2+ years' experience in FDA / ISO 9000 regulated environment.
Proven experience in the management of QA systems.
Ideally candidates will be experienced in product verification & process validations.
Strong Project Management skills required.
Please phone Larry on +353 1-2302400 / email@example.com
The RFT Group: Biopharmaceutical Division specialise exclusively in the recruitment of scientists, engineers and executives for the biotechnology, pharmaceutical and medical device sectors. www.rftgroup.ie / www.meddevicejobs.ie
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Key words; FDA, GMP, Quality Assurance, Quality Management, Compliance, Six Sigma, Process Validation, CAPA, DOE, New Product Introduction, Pharmaceutical, Medical Devices, Limerick, Cork, Tipperary, Waterford, Munster.