Pharma Manufacturing Technician – GMP & High-Potency

Piramal Pharma Limited; Grangemouth; A distancia; GBP 26.000 - 36.000; Jornada completa

Descripción de la vacante

Piramal Pharma Solutions in Grangemouth, UK, is seeking a Manufacturing Technician to support the production of high-potency pharmaceuticals in a cGMP environment. You will prepare and monitor manufacturing suites, maintain batch records, and ensure audit readiness.

The role requires 1–3 years of pharmaceutical manufacturing experience, GMP awareness, and the ability to work within a team across shifts, including evenings, weekends, and holidays.

Formación

• High school diploma or equivalent required; associate degree or technical certification preferred in manufacturing, biotech, or related field.
• 1–3 years of experience in a pharmaceutical, biotech, or medical device manufacturing environment.
• Familiarity with GMP/Regulatory requirements and SOPs; strong documentation discipline.

Responsabilidades

• Operate and maintain manufacturing equipment (mixers, blenders, tablet presses, encapsulation lines, packaging lines).
• Perform in-process checks and record data according to batch records and SOPs.
• Execute cleaning and sanitization of equipment and production areas.
• Prepare and stage raw materials and components for production runs.
• Troubleshoot minor equipment issues; escalate complex problems to maintenance or supervisors.
• Adhere to safety, quality, and GMP standards; ensure audit readiness.
• Complete batch records, logbooks, and incident reports accurately and timely.
• Participate in continuous improvement initiatives to enhance efficiency and throughput.
• Assist with calibration and preventative maintenance activities as required.
• Communicate effectively with team members, supervisors, and other departments.

Educación

High school diploma or equivalent

Associate's degree or technical certification

Descripción del empleo

Piramal Pharma Solutions in Grangemouth, UK, is seeking a Manufacturing Technician to support the production of high-potency pharmaceuticals in a cGMP environment. You will prepare and monitor manufacturing suites, maintain batch records, and ensure audit readiness.

The role requires 1–3 years of pharmaceutical manufacturing experience, GMP awareness, and the ability to work within a team across shifts, including evenings, weekends, and holidays.