QC Documentation Analyst I – Data & Records (GMP)

RoslinCT; City of Edinburgh; On-site; GBP 26,000 - 36,000; Full time

Benefits offered by this job

31 days annual leave + public holidays

Private healthcare

Group Life Cover

Company pension

Cycle2Work

Discounts

Job summary

RoslinCT in Edinburgh invites applications for a Quality Control Analyst I – DADM (Data & Documentation). This desk-based role involves preparing QC records, change controls and deviations, and ensuring GMP/SOP compliance.

You will author and update QC-related documents and compile certificates of analysis to support product release. You will also maintain records, assist with departmental projects, train junior colleagues, and provide after-hours support for critical equipment alarms as

Qualifications

• Prior experience working with scientific GMP documentation in chemicals or biological life sciences laboratory.
• A good standard of written English and the ability to write accurately and clearly.
• A good working knowledge of UK laws and regulations for cell therapy products and tissue donation.
• Proficient in the use of Microsoft Office applications.
• Strong communication and interpersonal skills, with the ability to develop and maintain effective working relationships.
• Skilled in managing and influencing stakeholder and customer expectations.
• Highly organised, with the ability to prioritise and manage multiple tasks in a fast-paced environment.
• Excellent attention to detail, ensuring accuracy and consistency in all work.

Responsibilities

• Prepare and complete quality-related documentation, including QC records, change controls, deviations, and risk assessments, in line with GMP and SOP requirements.
• Author, review, and update SOPs, forms, and other documentation relating to QC activities.
• Compile QC reports and certificates of analysis to support product release and regulatory compliance.
• Conduct general record keeping and maintain document organisation.
• Support with any departmental projects as required.
• Assist in the training and development of junior team members.
• Comply information used to communicate with clients.
• Provide out of hours cover, as required on a rotational basis, for critical equipment alarms.

Skills

GMP documentation

Quality control documentation

Microsoft Office

Communication skills

Education

Degree in Life Sciences

Job description

RoslinCT in Edinburgh invites applications for a Quality Control Analyst I – DADM (Data & Documentation). This desk-based role involves preparing QC records, change controls and deviations, and ensuring GMP/SOP compliance.

You will author and update QC-related documents and compile certificates of analysis to support product release. You will also maintain records, assist with departmental projects, train junior colleagues, and provide after-hours support for critical equipment alarms as