pharmaceutical procurement manager 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,...

A leading transportation company located in Larbert is seeking an experienced Commodity Manager to develop procurement strategies for key components. The ideal candidate will have extensive experience in strategic sourcing and supplier relationship management, ideally within the automotive sector. This role offers a competitive salary and a range of benefits aimed at supporting employee...

A leading sustainable transportation company in Scotland is seeking a Commodity Manager to develop procurement strategies for key components. The ideal candidate will have significant experience in strategic sourcing and supplier relationship management in the automotive sector, with strong negotiation and decision-making skills. This role offers competitive salary and benefits in a supportive...

Job Overview At 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...

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,...

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 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 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 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 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 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.