VQ Life Sciences are recruiting for a Permanent Quality Manager with experience of the pharmaceutical industry and regulations for a client based in London.
1. The Company
Our client is a company that provides temperature validation and monitoring solutions to the Pharmaceutical & Biotech Industries. We operate in a heavily regulated environment working with a wide range of companies from Labs, Hospitals, Wholesalers and Pharmaceutical manufacturers.
2. The Role
Responsible for managing and maintaining the ISO9001:2015 Quality Management System Accreditation, promoting compliance and quality assurance throughout the company. Manage all quality related activities. To include Quality Document Control, ensuring that processes and procedures support the quality management system.
3. General Role Responsibilities:
Translating the Quality Policy into an effective Quality Management System
Verify that approved quality system procedures are implemented, and where necessary, complementary procedures are raised, updated, and controlled.
Support the Operations Director to ensure that all administrative tasks linked to all technical aspects - methods, capabilities and competencies and carried out effectively and to a high standard.
Assist in implementing other ISO standards (ISO17025 UKAS)
Complete & archive all necessary QMS & QA forms.
Check and approve certificates and reports.
Ensure that the appropriate personnel are familiar with quality documents.
Manage and participate in internal and on-site audits.
Ensure the monitoring of customer feedback and satisfaction.
Conduct audit of approved suppliers.
Ensure that only approved procedures and documents are adopted and highlight any need for change.
Report the principal causes of quality deficiencies, operational non-conformances, and complaints.
Manage customer and supplier quality issues within the QMS.
4. The Ideal applicant must:
Be Process orientated
Have a High level of attention to detail
Have Excellent communication skills and an ability to build strong working relationships
Ability to translate technical concepts
Analytical mindset and the ability to process data
Experience of service delivery in a QMS environment
Excellent understanding of the UKAS standard and methodology
Comprehensive understanding of measurement and instrumentation.
Excellent knowledge of systems, software, technologies, communications, and suppliers to support the delivery of quality management system
Position Type: Full Time. POSSIBILITY TO START PART TIME FOR THE FIRST YEAR.
If you are a permanent Quality Manager based in London, with experience of the pharmaceutical industry and regulations then get in touch with Alex Prew at VQ Life Sciences
Document Management Systems
Quality Management Systems
Product Quality Assurance