quality lead jobs in Grangemouth

You will be at the heart of our analytical development efforts, playing a key role in supporting new drug development, scale-up, and commercial manufacturing. You’ll lead and contribute to technical projects that directly impact quality, efficiency, and regulatory compliance.

Job Title: Group Supplier Quality Engineer Location: Larbert, Scotland Our Vision & Why It Matters At Alexander Dennis, our vision is to lead the evolution of sustainable on-road mass transportation and mobility. We design, deliver, and support market-leading buses and coaches that help reduce emissions, improve air quality, and keep communities connected. Every role contributes to that...

Lead Engineer Job ID 247423 Posted 10-Nov-2025 Role type Full-time Areas of Interest Building Management, Engineering/Maintenance, Facilities Management Location(s) Grangemouth - Scotland - United Kingdom of Great Britain and Northern Ireland CBRE Global Workplace Solutions is a leading global provider of integrated facilities and corporate real estate management. We are recruiting a Lead...

A leading engineering and maintenance provider in the UK is seeking an Insulation Superintendent to oversee the planning and execution of all insulation activities on-site. The role demands a proven track record in a similar position with strong leadership skills, and the ability to manage teams while enforcing safety and quality standards. Essential qualifications include trade certification in...

Lead Fitter - Alloa Is your CV ready If so, and you are confident this is the role for you, make sure to apply asap. Our client, who are based in Alloa, and are a global leader in flow control solutions, is seeking an experienced Lead Fitter to work closely with department Team Leaders and Supervisors to ensure all work is carried out in a timely manner and to the required quality...

You will have a working knowledge in commercial or financial controls and be comfortable with managing financial performance, KPI’s and budgets. A qualification or relevant experience in business management would also be desirable. - Experience of managing remote field-based teams is essential to this role alongside having the ability to deal with the full spectrum of people management.

You will lead the verification, attributes and engineering quality function, owning the RHS of the Engineering System V. This includes digital and physical validation of vehicle requirements, homologation activities for new and ongoing projects, and delivery of engineering solutions to meet annual quality targets.

Scottish Canals are the custodians of the nation’s canal network and surrounding estates. Our vision is to invest in the canal network to generate lasting benefit for people and communities; celebrating their industrial heritage, ensuring they offer quality green and blue spaces for people and communities and contribute to Scotland’s resilience in tackling climate change. Our success is rooted...

A leading care home provider in Falkirk is seeking a dedicated Registered Nurse to join their team. This role involves ensuring high standards of person-centred care, conducting assessments, and mentoring junior staff. Candidates must hold a valid NMC License and have at least one year of nursing practice. Competitive pay rates, flexible pay, and professional training opportunities are offered....

You will be responsible for delivering your teams performance and driving quality assurance in line with company and the Financial Conduct Authority processes and standards. Your role will also focus on coaching, motivation and team productivity while providing feedback and insight on complaints root cause and recommending solutions to help reduce complaints volumes to all stakeholders.

Job Title: Group Supplier Quality Engineer Location: Larbert, Scotland Our Vision & Why It Matters At Alexander Dennis, our vision is to lead the evolution of sustainable on-road mass transportation and mobility. We design, deliver, and support market-leading buses and coaches that help reduce emissions, improve air quality, and keep communities connected. Every role contributes to that...

You will generate all required technical and process documentation and work within the Piramal Quality Management System (QMS) to ensure adherence to company and regulatory standards.

You will also lead and manage the implementation of improvements identified through CAPA actions and end-of-campaign reviews.

You will provide quality oversight for Antibody–Drug Conjugate (ADC) and other bioconjugate drug substances/products in clinical activities, ensuring regulatory readiness while partnering with site functions to embed quality into day-to-day operations. This role is ideal for a QA leader who thrives in collaboration, governance, and proactive quality improvement.

You will be at the heart of our analytical development efforts, playing a key role in supporting new drug development, scale-up, and commercial manufacturing. You’ll lead and contribute to technical projects that directly impact quality, efficiency, and regulatory compliance.

You will generate all required technical and process documentation and work within the Piramal Quality Management System (QMS) to ensure adherence to company and regulatory standards.

You will also lead and manage the implementation of improvements identified through CAPA actions and end-of-campaign reviews.

You will generate all required technical and process documentation and work within the Piramal Quality Management System (QMS) to ensure adherence to company and regulatory standards.

You will also lead and manage the implementation of improvements identified through CAPA actions and end-of-campaign reviews.

You will be at the heart of our analytical development efforts, playing a key role in supporting new drug development, scale-up, and commercial manufacturing. You’ll lead and contribute to technical projects that directly impact quality, efficiency, and regulatory compliance.

You will be at the heart of our analytical development efforts, playing a key role in supporting new drug development, scale-up, and commercial manufacturing. You’ll lead and contribute to technical projects that directly impact quality, efficiency, and regulatory compliance.

You will generate all required technical and process documentation and work within the Piramal Quality Management System (QMS) to ensure adherence to company and regulatory standards.

You will also lead and manage the implementation of improvements identified through CAPA actions and end-of-campaign reviews.

You will generate all required technical and process documentation and work within the Piramal Quality Management System (QMS) to ensure adherence to company and regulatory standards.

You will also lead and manage the implementation of improvements identified through CAPA actions and end-of-campaign reviews.