manufacturing bom engineer jobs in Grangemouth

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 adhering to defined cGMP procedures to manufacture high potency ADC/APIs in support of launched products and clinical trial programmes. Proactive approach to suite readiness, structured monitoring, line clearance, BOM/stock levels, sample control and SAP inventory.

Job Title: Manufacturing Engineer Location: Larbert 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 mission whether you’re...

A leader in sustainable transportation seeks a Manufacturing Engineer to enhance production efficiency and quality. The ideal candidate has strong mechanical or electrical expertise, experience with NPI, and a proactive approach to problem-solving. Join a team dedicated to reducing emissions and improving air quality through innovative transportation solutions. Competitive salary and...

FINTEC Recruit are recruiting Electrical Engineers for their well established manufacturing client based in the Stirling area. If the following job requirements and experience match your skills, please ensure you apply promptly. These are permanent positions working shifts based on a 5-shift rota (average 38 hours/week, 18 shifts over a 35-day cycle) Role & Responsibilities: - Electrical...

Join a market-leading confectionery manufacturer with 18 years of proven success in creating premium sweet treats in a dynamic production environment. Join an award-winning confectionery manufacturer with 18 years of sweet success, producing high-quality fudge and tablet in a fast-paced production environment. Hours: Monday to Friday, 7:00am 3:00pm Pay Rate: £18.29 per hour TM Scotland...

Job Title: Electrical Engineer Location: Grangemouth Contract Type: Permanent*UK RIGHT TO WORK REQUIRED* About the Role: Reporting to the Electrical Engineering Team Leader, the post holder will provide Electrical Engineering support to various assets. Role Responsibilities:Electrical Engineering focal point for the DHP site, day to day operations, breakdowns, Turnaround (TAR) and site Outage...

Maintenance Engineer Salary: Competitive salary Benefits: Company share save scheme, Pension up to 8% matched, Life insurance up to 4x salary Location : Bo'ness Ways of Working: Site based Hours of work :4 on 4 off 5:30-17:30/17:30-5:30 Contract Type - Permanent Why Greencore? Following the combination with Bakkavor in January 2026, we're one of the UK's leading creators of convenience...

You will be adhering to defined cGMP procedures to manufacture high potency ADC/APIs in support of launched products and clinical trial programmes. Proactive approach to suite readiness, structured monitoring, line clearance, BOM/stock levels, sample control and SAP inventory.

Job Title: Manufacturing Engineer3> Location: Larbert 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 mission whether you're...

Job Description Join a market-leading confectionery manufacturer with 18 years of proven success in creating premium sweet treats in a dynamic production environment. Join an award-winning confectionery manufacturer with 18 years of sweet success, producing high-quality fudge and tablet in a fast-paced production environment. Hours: Monday to Friday, 7:00am 3:00pm Pay Rate: £18.29 per...

You will be adhering to defined cGMP procedures to manufacture high potency ADC/APIs in support of launched products and clinical trial programmes. Proactive approach to suite readiness, structured monitoring, line clearance, BOM/stock levels, sample control and SAP inventory.

You will be adhering to defined cGMP procedures to manufacture high potency ADC/APIs in support of launched products and clinical trial programmes. Proactive approach to suite readiness, structured monitoring, line clearance, BOM/stock levels, sample control and SAP inventory.

You will be adhering to defined cGMP procedures to manufacture high potency ADC/APIs in support of launched products and clinical trial programmes. Proactive approach to suite readiness, structured monitoring, line clearance, BOM/stock levels, sample control and SAP inventory.

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 adhering to defined cGMP procedures to manufacture high potency ADC/APIs in support of launched products and clinical trial programmes. Proactive approach to suite readiness, structured monitoring, line clearance, BOM/stock levels, sample control and SAP inventory.

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 adhering to defined cGMP procedures to manufacture high potency ADC/APIs in support of launched products and clinical trial programmes. Proactive approach to suite readiness, structured monitoring, line clearance, BOM/stock levels, sample control and SAP inventory.