Inspection Technician

Merck; Milton Keynes; On-site; GBP 20,000 - 25,000; Part time

Job summary

A leading healthcare company is seeking a Production Inspection Technician in Milton Keynes. This role involves inspecting finished products for defects while adhering to GMP and SOP. The ideal candidate will have a strong attention to detail and interest in science. Full training will be provided, along with a necessary eye test. Applicants must be ready for flexible duties as needed.

Qualifications

• Interest in a scientific field.
• Understanding of product quality through GMP.
• Excellent attention to detail and ability to follow SOP.

Responsibilities

• Inspect finished product for defects.
• Follow SOP and batch paperwork.
• Support cleaning requirements in the area.

Skills

Accountability

Analytical Problem Solving

Attention to Detail

GMP Operations

Safety Standards

Education

GCSE/ A level (or equivalent)

Job description

Overview

Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork.

We are recruiting a Production Inspection Technician within our manufacturing facility in Milton Keynes. All work must be performed in accordance with current GMP (Good Manufacturing Practice) and local SOPs (Standard Operating Procedures). Attention to detail is critical for this role. Full training will be given on all tasks.

Responsibilities

• Inspecting finished filled product (animal vaccine) for defects
• Follow SOP and Batch paperwork instructions for completion of job tasks
• To be flexible to Business needs, train and work in other areas as required
• Support cleaning requirements in the Area
• To maintain safe working practices at all times

Qualifications

• GCSE/ A level (or equivalent), with an interest in a scientific field
• Understanding of product quality, for example: demonstrated through Good Manufacturing Practice (GMP)
• Evidence of excellent attention to detail and ability to follow Standard Operating Procedures (SOP)
• Good level of written and spoken English
• An up to date eye test (within 12 months) is necessary for this role

You will need to pass a short test identifying various defects for this role

Current Employees apply HERE

Current Contingent Workers apply HERE

Additional Information

Employee Status: Project Temps (Fixed Term)

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements: Not Applicable

Shift:

Valid Driving License:

Hazardous Material(s):

Required Skills: Accountability, Analytical Problem Solving, Biological Manufacturing, Business Management, Cleanroom Gowning, Cognitive Flexibility, Computer Literacy, Documentations, GMP Operations, Good Manufacturing Practices (GMP), Laboratory Processes, Machinery Operation, Management Process, Manufacturing Quality Control, Occupational Health and Safety Management, Packaging Operations, Pharmaceutical Manufacturing, Processing Paperwork, Process Safety, Production Scheduling, Safety Assurance, Safety Standards, Shift Work

Preferred Skills:

Job Posting End Date: 10/3/2025

*A job posting is effective until 11:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the end date.