Quality Control Analyst I – DADM (Data & Documentation)

RoslinCT; City of Edinburgh; Presencial; GBP 26.000 - 34.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Salary package

31 days annual leave

Company pension

Group Life Cover

Private healthcare

Cycle2Work scheme

Retail discounts

Descripción de la vacante

RoslinCT is recruiting for a Quality Control Analyst I – DADM (Data & Documentation) to join their Edinburgh team at Edinburgh BioQuarter. This desk-based role focuses on preparing quality documents and maintaining QC records in line with GMP/SOPs.

The ideal candidate has GMP documentation experience in life sciences, strong English writing skills, and proficiency with Microsoft Office. The role offers a competitive package and long-term development opportunities.

Formación

• Experience with scientific GMP documentation in chemicals or biological life sciences.
• Strong written English with clarity and accuracy.
• Knowledge of UK laws and regulations for cell therapy products.
• Proficient in Microsoft Office applications.
• Excellent communication and stakeholder management.
• Highly organized, able to prioritise multiple tasks.
• Degree in Life Sciences or equivalent.

Responsabilidades

• 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.

Conocimientos

GMP documentation

Microsoft Office

Written communication

Attention to detail

Educación

Degree in Life Sciences

Descripción del empleo

Quality Control Analyst I – DADM (Data & Documentation)

Location: Edinburgh BioQuarter

Who are we?

We are RoslinCT, a world-leading cell and gene therapy contract development and manufacturing organisation creating cutting-edge therapies that change people’s lives.

Collaborative, dedicated and talented people are the backbone of our culture, working both autonomously and in driven teams to make life-changing products utilising ground-breaking science.

Find out more about what we do here!

Due to the nature and training requirements of this role, applicants must have the legal right to work in the UK with sufficient permission to meet the needs of the position. We are unable to provide visa sponsorship for this role under the Home Office restrictions.

Why join us?

• The opportunity to join a rapidly expanding company which is changing lives, giving you the skills and experience to develop your career.

• A generous salary package – we reward our people at the level they deserve.

• 31 days of annual leave, plus 4 public holidays which increases with tenure.

• A competitive company pension scheme to help you save for the future.

• Group Life Cover – you are automatically covered for three times your basic salary to give you and your family peace of mind.

• Private healthcare and access to mental health/wellbeing support as your health and wellbeing means a lot to us.

• Flexible benefits such as retail discounts and access to the Cycle2Work scheme.

Your new role

• An exciting opportunity for a Quality Control Analyst I – DADM (Data & Documentation) to join our team.

• Please note: although this role is within QC, this is a desk-based position, so it doesn't involve any testing in the lab.

• 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.

About you

• 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.

Qualifications

A Degree in Life Sciences. An equivalent qualification or relevant experience will be considered.

At RoslinCT, we’re all about inclusivity and creating a fair, welcoming workplace. Our goal is to make sure everyone knows they’re valued and encouraged to be themselves, whether they’re our employees, customers, or partners.

We take pride in being an equal opportunity employer. We treat all applicants fairly and don’t discriminate based on any protected characteristics. So, no matter who you are, we welcome your application with open arms.

If you’ve got any specific needs or concerns regarding accessibility during the recruitment process, don’t hesitate to reach out to us at [e-mail]. We’re here to assist and make things as smooth as possible for you.