Scott McIntee

Managing Consultant
  1. 01384 446180
  3. Linkedin profile
  4. @JonLee_Recruit

Scott is responsible for the day to day operational management of the engineering, manufacturing and commercial team. He has successfully supported specialist SMEs right through to some the world’s leading corporate organisations in their recruitment across both engineering and procurement disciplines.

Scott has been recruiting for over 10 years, after a sucessful career in automotive supply chain and procurement, Scott has a breadth of recruitment experience across various engineering and commercial disciplines to include operations, engineering, supply chain, quality, design and development from graduate level through to senior management.

Scott’s key strength over the last decade has been to develop excellent working relationships with clients; taking the time to really understand their specific needs before going to market.

Scott’s consultative approach and ability to market roles to passive candidates has ensured his clients have access to the most skilled individuals.

Browse Scott's latest jobs

Senior Quality Engineer - Management Systems

My client a well respected international medical device manufacturer are seeking an experienced Senior Quality Engineer Management Systems. The primary responsibility of the role is to organise and lead on a day to day basis the company's quality systems, to the requirements of regulated standards. To maintain certification to these standards as required, by administration of the management system, driving actions and facilitating others to ensure compliance.The job role is best suited to a very motivated, well organised person. The individual will lead and work with various departments in order to develop integrated processes and procedures which work for the business, but comply with the requirements of standards. Core Responsibilities Implement and maintain the company's Business Management Systems ensuring compliance to ISO9001, 14001, OHSAS 1800/ISO 45001 and ISO 13485 and FDA QSR requirements. Support the transition to 45001 in conjunction with the HSE Advisor Implementing ISO 13485 Liaising with external certification bodies (or enforcing agencies such as FDA) to maintain/again certification and approval as required Management and implementation of the internal audit programme for QHSE, including ad hoc process audits as the need demands, including ensuring legal compliance audits are conducted as required. To locally implement and monitor Group QHSE Policies and Processes, ensuring embedding and approval of all QHSE documents Ensuring DMR information is suitably controlled and issued Lead the internal audit program, conduct internal audits and drive associated improvement activity. To be the representative for system and product certification audits and reporting. Experience Required Auditing experience in any of: ISO 9001, ISO 45001, ISO 14001 and ISO 13485 and FDA Part 820 Quality System Regulation - ideally lead auditor trained Medical device regulatory experience or qualification Knowledge of ISO9001 Knowledge of any of: ISO 45001, ISO 14001 and ISO 13485 and FDA Part 820 Quality Systems is desirable not essential Medical Device quality systems, implementation would be beneficial This role would suit an experienced Quality Engineer or Senior Quality Engineer seeking to progress their career in Quality Systems Management. Please apply as soon as possible to be considered for this desirable Quality Engineering position.

Permanent / Dudley, West Midlands

Quality Manager

A leading manufacturer of medical devices is seeking a dynamic Quality Manager in order to develop, organise and manage the company's quality system and quality team. The job role is best suited to a very motivated, well organised person with management experience and excellent communication skills, for both internal and external communication. You will need to be driven to make substantive improvement to the quality department. Quality Manager Responsibilities: Act as a change agent for the rapid evolution from a quality control to a quality assurance structure. The drive and energy to lead transformative change in the way we approach quality building it in to processes and design. To build and develop a new quality team focused on identification of issues and root causes, addressing them and delivering permanent improvement. Coaching them to continually improve themselves and the business. Manage and facilitate corrective and preventive actions required for QHSE, ensuring all product related issues, customer complaints/Accidents, Incidents etc. driving through to closure. Establish automated reporting on performance against KPI's and regulatory reporting for QHSE. Administer and support, including regulatory reporting the established group policy for the FDA and EHS certifications as well as applicable statutory reporting for the KWF site e.g. FDA, HSE, the Environment Agency etc. Take the lead in any complex investigations as appropriate. Ability to analyse data and information, both numerical and anecdotal to determine plan of action and carry it out. As the company representative implement and maintain the company's Business Management Systems ensuring compliance to ISO9001, 14001, OHSAS 180001/ISO 45001 and ISO 13485 and FDA QSR requirements as appropriate. Assist in new product introduction from design stage through to production. Quality Manager experience and abilities required: Experienced Quality Manager ideally with a electro-mechanical medical device industry background. Other electro-mechanical industry backgrounds will be considered. Strong leadership and coaching skills Experience in implementation and maintenance of Business Management Systems ensuring compliance to ISO9001/14001 New product introduction H&S, Environmental and Quality Legal and Regulatory Knowledge Knowledge of quality systems related to medical devices - FDA/ISO 13485 or other highly regulated industry is desirable although not essential Knowledge of EH&S systems and legal requirements Strong IT skills Excellent interpersonal skills at all business levels Good presentation/ communication skills Great prioritising and managing high workload ability Analysing and interpreting data and good reporting skills NEBOSH is desirable Strong engineering (ideally electro-mechanical) background and education Please apply as soon as possible to this highly desirable Quality Manager role with a leading medical device manufacturer.

Permanent / Dudley, West Midlands

Plant Manager

A significant opportunity has arisen for an experienced Plant Manager to take up overall responsibility for a 450 employee heavy industry manufacturing plant in the Northampton area. This is a challenging and demanding role, offering the successful candidate a highly competitive remuneration package, reflective of the responsibilities and status of this senior management level position. The Role As the Plant Manager you will have responsibility for circa 450 employees on a large 24/5 manufacturing site and hold full financial responsibility for the site with a large financial turnover. In this capacity, you will be required to provide direction across all areas, ensuring company objectives are met and enabling new product development. Your key responsibilities and accountability's, will include, but not be limited to the following: To develop and embed a Lean Manufacturing / continuous improvement environment, in a complex culture, dealing with objections and a large work force. To develop relationships with Unions to improve employee engagement, resolve challenging issues and effect positive cultural change. To take overall responsibility for customer delivery, including direct interaction with customers as required. To effectively manage a challenging maintenance schedule To hold accountability for QHSE strategy and ensuring all relevant and legislative standards are met by the operations. The Candidate To be considered for this opportunity, you will require: Significant experience of successfully implementing and managing change in a complex environment Experience of working at Senior Management level within a Unionised environment Experience of holding full budgetary responsibility for a site with a turnover exceeding £100m In depth knowledge of Lean manufacturing/continuous improvement tools & techniques and able to evidence the successful implementation of these Able to evidence the ability to deal with complex challenges with positive results Experience in Heavy Industry Strong Leadership & communication skills Courage in decision making and management, with the ability to influence at all levels NEBOSH or equivalent H&S qualification High levels of energy, drive and resilience Ideally degree-level education in a relevant Engineering or Technical discipline (MBA an advantage) Please apply as soon as possible to be considered for this highly desirable Plant Manager opportunity.

Permanent / Northamptonshire, England


don't take our word for it...

  • The automation team at Jonathan Lee has taken the time to understand our business requirements, developing local relationships with the individual sites via visits to our locations to ensure the quality of candidates is of a high standard. Furthermore, Jonathan Lee has attributed a member of its Client Services team to act as a senior level contact for Knapp. This ensures there is a high-level of pro-active engagement with us as a customer not only in the traditional recruitment process but also in areas that can indirectly contribute to our business relationship. Should anyone be looking for a recruitment partner with in-depth industry knowledge in automation that operates in an ethical, partnership-based manner I can highly recommend the team at Jonathan Lee.

    Alexia English

    Human Resources Manager