Validation Technician

Euro-projects Recruitment Ltd; Newark on Trent; On-site; GBP 25,000 - 35,000; Full time

Job summary

A recruitment agency is seeking a Validation Technician in Newark on Trent. This role offers flexible working hours and full training in validation and machinery compliance. You will support validation processes in medical and pharmaceutical manufacturing, ensuring compliance with quality systems. Ideal candidates display attention to detail and a willingness to learn. Experience in regulated sectors is beneficial. The position provides opportunities for growth within a stable environment.

Benefits

Flexible hours

Full training provided

Qualifications

• Some experience with documentation in an engineering or manufacturing setting.
• Willingness to learn and develop skills.
• Exposure to highly regulated sectors is beneficial.

Responsibilities

• Support validation activities and machinery compliance.
• Collaborate on validation processes for new products.
• Engage with teams in regulated sectors.

Skills

Attention to detail

Cross-business validation

Job description

Overview

Validation Technician – Flexi time. Finish at 12:00 on Friday. Role is validation, machinery compliance, and technical documentation with full training provided.

Location and hours

Based near Southwell with commutable options from Southwell, Newark, Lincoln, Tuxford, Nottingham, Mansfield, Hucknall, Heanor. The role includes flexible hours with early finish on Friday (e.g., 7:00 to 15:30 or similar Monday to Thursday and Friday 12:00 finish).

Role context

Mechanical precision components into Medical and pharma manufacturing / engineering (plus aerospace, semiconductor and highly regulated industries). Opportunities for growth and stability within the company.

Responsibilities

• Support validation activities, machinery compliance, and maintenance of technical documentation (full training provided).
• Collaborate across the business on validation processes for new products and quality systems.
• Engage with teams in regulated sectors and contribute to process conformance and FAT/validation activities as appropriate.
• Act as a capable contributor in a 150–200 headcount SME environment with a hands-on, doer mentality.

Essential Experience

• Full training provided.
• Some experience with documentation in an engineering or manufacturing setting (quality systems, compliance, SOPs, FAT, validation).
• You do NOT need to be an engineer; attention to detail and cross-business validation work are key.
• Demonstrated willingness to learn and develop skills.
• Exposure to highly regulated sectors (aerospace, oil and gas, nuclear, medical, pharmaceutical, automotive) would be beneficial.
• Experience in a mid-size SME environment with a practical, hands-on approach.

Please note that if you are not contacted within the next ten days then your application has not been successful on this occasion. We thank you for taking the time to apply.