Technical Administrator

Quanta Consultancy Services Ltd; Swindon; On-site; GBP 28,000 - 40,000; Full time

Job summary

Quanta Consultancy Services Ltd in Swindon seeks a Technical Administrator for a 12-month initial contract. The role involves supporting validation activities, reviewing GMP documentation, and preparing requalification records as part of a fast-paced life sciences project lifecycle.

You will assist with technical paperwork and validation deliverables, conducting first-pass reviews before the facilitator review and helping with junior validation tasks across the team.

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.

Skills

Validation experience

Document review

GMP knowledge

Attention to detail

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. This is the chance to get involved with a global client who is going from strength to strength. 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.