GMP Quality Assurance Technician | Process & Compliance

Piramal Pharma Ltd; Grangemouth; On-site; GBP 24,000 - 34,000; Full time

Job summary

Piramal Pharma Solutions is seeking a QA Technician to support QA activities across GMP manufacturing, testing and documentation. The role involves reviewing procedures, batch records, change controls and deviations, and acting as QA representative for campaigns to ensure cGMP compliance.

You will collaborate with Operations, QC, MSAT, Supply Chain and Regulatory functions to resolve quality issues efficiently, prepare QA documentation for audits, and promote a culture of continuous improvement

Qualifications

• Assist QA officer in review of procedures and batch paperwork, ensuring accuracy and compliance.
• Act as QA representative for campaigns involving change control, deviation, validation and audits.
• Identify and elevate cGMP issues with potential impact on batch quality.

Responsibilities

• Provide QA support to GMP manufacturing, testing, and related activities.
• Review and approve master/executed batch records, validation and GMP documentation to ensure accuracy and completeness.
• Support deviation management from initiation, investigation to closure.
• Review and approve QMS records, including deviations, change controls, CAPAs, and risk assessments.
• Support material status control and batch lifecycle activities, including readiness for batch disposition.
• Ensure adherence to data integrity principles and GMP requirements across all activities.
• Support regulatory inspections, client audits, and internal audits through QA documentation.
• Collaborate with Operations, QC, MSAT, Supply Chain, and Regulatory to resolve quality issues efficiently and compliantly.
• Promote a strong quality culture and continuous improvement mindset on site.

Skills

QA knowledge

GMP

Documentation

Audit support

Collaboration

Job description

Piramal Pharma Solutions is seeking a QA Technician to support QA activities across GMP manufacturing, testing and documentation. The role involves reviewing procedures, batch records, change controls and deviations, and acting as QA representative for campaigns to ensure cGMP compliance.

You will collaborate with Operations, QC, MSAT, Supply Chain and Regulatory functions to resolve quality issues efficiently, prepare QA documentation for audits, and promote a culture of continuous improvement