Master Scheduler

Description

• The management, and operation, of all aspects of new and current research and development
• To ensure the regulatory compliance of the company and the products
• To maintain close working relationships with operational personnel to enable effective, timely resolutions of technical and quality issues and promote continual improvements.
• To oversee the development of, and continuously improve the company's QMS, with the target of maintaining accreditations to standards, including Medical Devices (ISO 13485), Cosmetics GMP (ISO 22716) and ISO 9001.

• Product development through the implementation of a product development process, by managing internal and external resources, from consumer insights through to launch of products
• Plan and deliver product designs which meet specified performance and cost criteria within development budget and timetable
• Technical and quality support - both internally to sales and production, and externally to assisting and potential customers including legal/mandatory as well as technical guidance
• Chemicals laboratory in support of operations.
• Ensuring technical compliance to ISO standards and regulatory standards. Ensure the business is compliant with all Regulations with regard to CHIPS, REACH,ATEX, and EEC directives on Cosmetics, Biocides and Detergents
• To monitor and improve the quality of manufactured finished goods, including effective complaint management, investigation and resolution.
• To assist the factory in adhering to GMP that conforms to ISO standards, and to audit this
• To manage product specifications relating to set-up of new products and changes to existing products.
• To assist procurement/supply chain in ensuring that suppliers provide raw materials and components that meet the agreed and required standards.
• To support Sales in managing customer audits and assisting with other customer visits
• Maintain relationships with customers whilst offering a professional service