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Job Title - Mechanical Engineer

Location - St Helens

Are you a Mechanical Engineer with experience of maintenance engineering who would like to join a new company at the beginning of it's ambitious journey to commercial manufacturing ?

Salary Range - Open

Details/Brief - This is a full-time on-site role as a Mechanical Engineer. The Mechanical Engineer will be responsible for tasks such as mechanical and electrical engineering and maintenance, machine improvements, project management, PLC programming and research and development (R&D)

Qualifications

Mechanical Engineering and Machine Design skillsProficiency in PLC programmingExperience in Project Management and Research and Development (R&D)Strong analytical and problem-solving skillsAbility to work well in a team environmentQualified to level 3 in Mechanical EngineeringPrevious experience in the glass industry is a plus

Please contact Simon Fowler on 01925239725

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Manufacturing & Quality Manager - North Wales (Mold)

Maximum salary of £55k with a £5k increase after a successful probation.

4 days on site & 1 day working remotely.

NEW URGENT VACANCY for a Manufacturing Quality Manager - growing Medical Device organisation who make unique critical feeding systems for infants ... supplying hospitals worldwide.

North Wales with a registered office in Liverpool and plans to build a production facility in a more central Cheshire or Merseyside location with 6-12 months.

Products registered in UK, Italy & Europe (CE & CA Marked & regulated under ISO 13485)

Must have experience in the Manufacture of Medical Devices

Please contact Simon Fowler at NGAGE Smart4Sciences

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Smart4Sciences are currently working with a global analytical research and testing provider to recruit a Quality Manager GMP their MHRA, FDA AND UKAS regulated facility in Kent.

As a Quality Manager you will be a key part of the site leadership team and responsible for all QA functions including processes, systems and staff - liaising with other Quality Managers across the group to ensure a unified approach to quality across all global sites.

Key responsibilities

Oversee the site QA function, ensuring compliance with GMP, ISO 17025, FDA 21 CFR 820, and other regulatory standards.Lead a team of Quality Specialists, promoting a positive culture of quality compliance and upskilling staff members through regular coaching/trainingLead investigations, audits, non-conformances, and supplier quality to drive continuous improvement

Key Requirements

Significant experience in GMP Quality Assurance from the Pharmaceutical and/or Medical Device industries including management and leading of teamsA demonstrable background in continuous improvement with a proficiency in Six Sigma and Lean MethodologiesPrior experience in a CRO/CDMO environment with the ability to manage multiple priorities in busy project based environments.

Interviews for this Quality Manager position are imminent so please apply today or contact Gareth Gooley at Smart4Sciences for more information

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