Quality Assurance Technician

Pharmaceutical Manufacturing | Grangemouth | Shift-Based (Weekends Required)

Do you have a sharp eye for detail and a passion for getting things right? This is a chance to play a key part in making sure life-changing medicines are made to the highest standards.

We're recruiting a Quality Assurance Technician for a leading pharmaceutical manufacturer. You'll work at the heart of the QA team. You'll make sure every batch meets cGMP requirements before it reaches the patients who depend on it.

Please note: this is a shift-based role and includes weekend working.

What you'll be doing

• Supporting the QA Officer in reviewing procedures and completed batch paperwork, covering both manufacturing and analytical documentation
• Reviewing manufacturing, laboratory and associated documentation ahead of QP review and final product disposition, and flagging potential issues early
• Reviewing and approving documentation for incoming raw materials and updating SAP
• Generating and checking product and status labels
• Providing line clearance to support manufacturing activities
• Acting as the QA point of contact for SAP and material/component clearance, escalating issues to the QA Team Leader or QA Manager where needed
• Identifying and escalating any cGMP issues that could affect batch quality
• Checking QMS records for closure and keeping departmental systems up to date
• You'll work with colleagues in QC, Compliance and Production, as well as customers and suppliers. This is a varied role with real visibility across the site.

What we're looking for

• A BSc in a relevant scientific discipline (or equivalent)
• A minimum of 3 years' experience in a cGMP environment manufacturing Active Pharmaceutical Ingredients (APIs)
• Experience working with QA, analytical chemistry, development and manufacturing teams (beneficial)
• Excellent attention to detail
• Strong written and verbal communication skills
• Good organisation and the ability to prioritise your workload to meet deadlines
• The ability to analyse data, identify root causes and make considered decisions
• A team player who can also work confidently on your own initiative
• The confidence to follow instructions accurately and escalate issues when needed
• Flexibility to work a shift pattern, including weekends

Why apply?

• Join a global, integrated pharmaceutical network with strong development opportunities
• Work in a role where your attention to detail makes a real difference to patient safety
• Build your career in a growing Quality function

Ready to apply?
Send your CV today, or get in touch with us for a confidential chat about the role.

Guidant, Carbon60, Lorien & SRG - The Vertage Group Portfolio are acting as an Employment Business in relation to this vacancy.