Technical Administrator

QCS Staffing; Swindon; On-site; GBP 32,000 - 42,000; Full time

Job summary

QCS Staffing is seeking a Technical Administrator for a 12-month contract in Swindon within the Life Sciences sector. The role supports validation and requalification activities, with emphasis on document preparation and review of GMP paperwork in a regulated environment.

The position involves handling requalification documentation, assisting with validation tasks, and contributing to the full project lifecycle.

Qualifications

• Extensive experience within validation, laboratory systems or technical documentation.
• Experience supporting validation activities in a regulated environment.
• Knowledge of GMP documentation practices.
• Strong attention to detail and document review experience.

Responsibilities

• Support requalification activities through document preparation and updates.
• Review technical paperwork and validation documentation.
• Complete first-pass reviews prior to facilitator review.
• Assist with junior validation activities across the team.
• Prepare requalification documentation and associated records.

Skills

Validation experience

Lab systems

Technical documentation

Documentation review

Job description

Technical Administrator - UK, Swindon - Initial 12-Month Contract - Life Sciences

Would you like to support one of the largest CMO's in the world? Well look no further as we may have the opportunity for you!

Our client is seeking a Technical Administrator to support their project located in Swindon for an initial 12 month duration.

It is a fast paced and exciting environment which is seeing a lot of internal investment.

With several exciting refurbishment projects in the pipeline this is a great chance to be involved in the full project lifecycle with the opportunity to move into other projects and areas of the business.

What You'll Deliver

• Support requalification activities through document preparation and updates.
• Review technical paperwork and validation documentation.
• Complete first-pass reviews prior to facilitator review.
• Assist with junior validation activities across the team.
• Prepare requalification documentation and associated records.

Experience required:

• Extensive experience within validation, laboratory systems or technical documentation.
• Experience supporting validation activities in a regulated environment.
• Knowledge of GMP documentation practices.
• Strong attention to detail and document review experience.