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| Job Title |
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Pharmaceutical Engineering Quality and Validation |
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| Job number |
120142336 |
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| Posted |
15/07/2008 (14:11) |
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| Agency/Employer |
Quality Start |
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| Description |
Are you currently working in quality and validation? Have you defined and implemented a validation policy? Have you defined a validation life cycle of new and in-production products? Looking for your next career move? Yes, then you do not want to miss out on this one off fantastic opportunity.
Your role as a Quality and Validation Manager will involve managing my client’s validation function. You will draft and implement a validation policy and associated documentation design, maintenance and delivery. You will define a validation life cycle of new and in-production products in conjunction with my client’s business units. You will be liaising with suppliers and customers in the development of validation documents as well as managing the life cycles for development and customer contracts.
You will be working closely with the design team where you will contribute to product development relative to validation as well as attend and present my clients events and international seminars and conferences relating to pharmaceutical validation.
To apply for this role you will be educated to a degree level or equivalent within science or engineering. You will have excellent knowledge of, and experience in, pharmaceutical validation and ideally you will have managed people.
If this sounds like the role for you or a colleague then please don’t hesitate to contact us. Quality Start will offer £200 to anyone who successfully recommends a candidate who is subsequently employed by our client.
To apply for this one of opportunity, please send your CV to me now or call for a confidential chat.
If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role.
Quality Start are acting as a specialist recruitment consultancy for this role.
Skills:
Quality Systems Management, GMP, ISO 9001, ISO 13485, Internal Audit, Pharmaceutical Industry, Medical Devices Industry, Biotechnology Industry, Clinical Research Industry, Compliance, Regulatory Affairs, Quality Engineer, QA Engineer, FDA, MHRA, Six Sigma, External Audit, Internal Audit, QA, Quality Assurance, QP, Qualified Person, Documentation Control, CAPA, Change Control, Standard Operating Procedures, GLP, GxP, GCP, Orange Guide, FDA Part:21, Process Improvement, Manufacturing, Production, QMS, Corrective and Preventative Actions, Validation, Customer Complaints, Deviations, Supplier Audits, CRO, Project Management, Training, QMS.
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| Location |
North West , North West |
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| Job type |
Permanent |
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| Contract length |
N/A |
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| Salary/rate |
£34000 - £37000/annum Hols, pension, flexi hours, canteen |
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| Start date |
ASAP |
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| Contact name |
Selina Thompson |
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| Telephone |
0113 225 1547 |
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| Ref no |
QS0025 |
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| Apply |
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