Qa Technician

Srg; Grangemouth; On-site; GBP 26,000 - 38,000; Full time

Job summary

Pharmaceutical QA Technician role at Grangemouth requires a BSc in a relevant science and at least 3 years of cGMP API manufacturing experience. You will support QA, review batch paperwork and QC docs, and ensure compliance across manufacturing and analytical activities.

SAP familiarity and strong communication are essential. The position is shift-based, with weekend work, offering visibility across QA, Compliance and Production teams, and opportunities to impact patient safety and product

Qualifications

• A BSc in a relevant scientific discipline (or equivalent).
• A minimum of 3 years' experience in a cGMP environment manufacturing APIs.
• Experience working with QA, analytical chemistry, development and manufacturing teams (beneficial).
• Excellent attention to detail, strong written and verbal communication, and good organisation.

Responsibilities

• Supporting the QA Officer in reviewing procedures and batch paperwork across manufacturing and analytical documentation.
• Reviewing manufacturing, laboratory and related documentation ahead of QP review and final product disposition.
• 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 clearance, escalating issues as needed.
• Identifying and escalating any cGMP issues that could affect batch quality.
• Checking QMS records for closure and keeping departmental systems up to date.
• Collaborating with QC, Compliance, Production, customers and suppliers on a site-wide QA basis.

Skills

Attention to detail

Communication skills

Organisation

Data analysis

Team player

Education

BSc in a relevant scientific discipline

Tools

SAP

Job description

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 escal… 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