pharmaceutical granulation operator 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,...

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...

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: 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...

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...

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.

Bilfinger UK is a leading engineering and maintenance provider, supporting customers across the chemical & petrochemical, nuclear, oil & gas, pharmaceuticals & biopharma, power & energy, utilities, renewables and food & beverage markets. We enhance the efficiency of assets, ensuring a high level of availability and reducing maintenance costs. We have extensive experience in offshore and onshore...

Job Description 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...

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 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 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 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 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.