Pharma QA Technician: Weekend Shift for cGMP Excellence

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 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