risk manager jobs in Grangemouth

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.

About Us Scottish Canals are the custodians of the nation’s canal network and surrounding estates. Our vision is to care for and 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...

Connect Appointments have a fantastic permanent opportunity for a Logistics Administrator to join our Grangemouth based client (FK3)! What's on offer? - Full-time permanent position - Annual salary dependent on experience - Shifts starting from 7am - Great opportunities for career growth Working as a Logistics Administrator, your duties will include: - Accurately inputting and processing...

Overview Join to apply for the Corporate Tax Manager role at EQ Accountants, part of the Sumer Group . Location: Grangemouth | Department: Corporate Tax At EQ Accountants, part of the Sumer Group, we know our people are at the heart of everything we do. We're not just colleagues – we're a community. Our ethos, With You, means when our team thrives, our clients do too. We're committed to...

You must be eligible to work in the UK to apply for this vacancy. Cancer Research UK is not able to offer visa sponsorship. At Cancer Research UK, we exist to beat cancer. We are professionals with purpose, beating cancer every day. But we need to go much further and much faster.

5 days ago Be among the first 25 applicants This range is provided by FT Recruitment Group. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range FT Recruitment Group are recruiting on behalf of our client for a Commercial Manager based in either of their offices in Grangemouth, Warrington or Reading, on a Permanent, Full Time...

Technical Technologist 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: Monday-Friday 8:00-16:00 Contract Type: Permanent Why Greencore? Following the combination with Bakkavor in January 2026, we're one of the UK's leading creators of convenience food,...

You will support and implement the HS&E strategy and systems to ensure that the delivery of our operations meets exemplary safety, health and environmental standards. This role supports improvement and consistency in performance, ensuring compliance with management systems and implementing continual improvement initiatives across the framework.

Job Title: Principal Engineer – Technical Specialist – HVAC/Auxiliary Location: Scotstoun/Portsmouth/Filton. We offer a range of hybrid and flexible working arrangements. Please speak to your recruiter about the options for this particular role Salary: Up to £60,000 depending on skills and experience What you’ll be doing: - Support the Platform TA in requirements, acceptance, architecture and...

Support WorkerLocation: FalkirkContract Type: Permanent – Part time and Full time day shift positions availableSalary: £12.84 per hourAre you passionate about making a difference in people’s lives? Apply to be part of a dedicated team providing safe, secure, and supported accommodation for people experiencing homelessness. You’ll help individuals build independence, access opportunities, and take...

Connect Appointments have an exciting opportunity for an experienced Supervisor to join our Grangemouth-based client on a full-time, permanent 12-month contract. What's on offer? - Permanent role working 39 hours per week, Monday to Friday, 8am to 4:30pm (with an early Friday finish) - Competitive pay of 17.35 per hour, plus shift allowances, project bonuses, and enhanced overtime rates -...

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 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 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 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.