Pharmaceuticals 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 OverviewAt Piramal Pharma Solutions, we’re looking for a skilled and motivated Engineering professional to help maintain and improve our HPS plant and equipment. You’ll play a key role in ensuring assets operate safely, efficiently, and in line with qualified status, business needs, and design intent.You’ll report directly to the Engineering Manager and work as part of a collaborative,...

Join a dynamic pharmaceutical company where your supply chain expertise will directly impact the delivery of life-changing treatments. Supply Chain Administrator (Temp work, week to week) £12.50 per hour Grangemouth FK3 TaskMaster Grangemouth & Falkirk are excited to be working on behalf of one of our clients in Grangemouth who is seeking a highly skilled and detail-oriented Supply Chain...

Job Title: Pharmacist Manager Branch Address: 5 South Street, Bo'ness, EH51 0EA Hourly Rate: From 28.70 per hour Working Hours: 40.25 hours Week 1: Monday to Friday 42.5 hour week Week 2: Monday, Tuesday, Thursday and Friday PLUS Saturday (4 hour shift Saturday) 38 hour week Are you a dedicated and patient-focused Pharmacist looking for an exciting opportunity to lead a dedicated team and...

Senior System Integration Engineer BGEN Ltd, Grangemouth, Scotland, United Kingdom Job Details Seniority level: Mid‐Senior level. Employment type: Full‐time. Where will you be working? At M Group Water we help our clients safeguard the water supply, improve environmental performance and manage demand for future generations. We enhance and extend asset life, ensuring compliance with water...

Right across infrastructure, there's a requirement to not only maintain, but also renew and reimagine. Whatever stage you're at in your career, with us you'll have an opportunity to grow and develop. Delivering essential infrastructure services for life, while being safety first, and client and customer centric in a friendly, fun and respectful environment where you are encouraged to...

The Quality Technician will assist the QA officer in the review of procedures, completed batch paperwork including manufacturing and analytical documentation. Be the QA representative for new campaigns dealing with aspects including process instruction sheets, change control, deviation, validation, customer audits, raw material and final product disposition. The QA Technician is expected to...

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 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 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 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 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 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.