Quality Technician – GMP & Microbiology (Day Shift)

MTrec Ltd; Ashington; On-site; GBP 28,000 - 38,000; Full time

Benefits offered by this job

Annual bonus

OT opportunity

Company benefits

Job summary

MTrec Ltd, a specialist manufacturing client, seeks a Quality Technician for a permanent day shift at Ashington. You will support the Senior Quality Technician and carry out QC tests on raw materials, liquids, and finished products ensuring compliance with approved specs.

You will perform environmental monitoring, maintain records, and coordinate sampling with production. Strong GMP/QMS experience and auditing ability are required, alongside good IT skills.

Qualifications

• Experience of working in quality assurance roles, ideally in a GMP environment.
• Ability to perform QMS activities across site (e.g., Deviation management, CAPA, Change control).
• Experience of review and approval of validation and qualification documents essential.
• Microbiology experience beneficial.

Responsibilities

• Perform QC tests on raw materials, blended product, and finished products according to approved specifications.
• Carry out routine environmental monitoring of cleanrooms and sampling from the purified water system.
• Maintain accurate records and ensure all monitoring equipment is operated per procedures.
• Investigate deviations and out-of-spec results and help implement corrective actions.
• Work with production to drive site improvements and ensure GMP compliance.
• Order QC reagents and assist day-to-day QA activities.

Skills

Quality Assurance

GMP Experience

QMS

Auditing

Microbiology

Documentation

Communication

IT Skills

Tools

Microsoft Word

Excel

Outlook

Job description

MTrec Ltd, a specialist manufacturing client, seeks a Quality Technician for a permanent day shift at Ashington. You will support the Senior Quality Technician and carry out QC tests on raw materials, liquids, and finished products ensuring compliance with approved specs.

You will perform environmental monitoring, maintain records, and coordinate sampling with production. Strong GMP/QMS experience and auditing ability are required, alongside good IT skills.