Quality Assurance Officer II – 9-Month Fixed Term Contract at RoslinCT

Danderhall, Scotland, United Kingdom -

Full Time

Start Date

Immediate

Expiry Date

24 Jun, 26

Salary

0.0

Posted On

26 Mar, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

cGMP Principles, Data Review, Internal Audits, Supplier Evaluation, Customer Audits, Regulatory Inspections, Training Delivery, Quality Metrics Compilation, SOP Writing, Documentation Review, Risk Assessment, Decision Making, Continuous Improvement, Self-Motivation, Adaptability

Industry

Biotechnology Research

Description

Quality Assurance Officer II – 9-Month Fixed Term Contract Location: Shawfair 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! 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 Assurance Officer II to join our Quality team. This is a temporary contract. It is anticipated that the role will be effective from Apr 2026 till Jan 2027. You’ll be responsible for writing, reviewing and updating Standard Operating Procedures (SOPs) to ensure ensure alignment with company policies, current practices, and applicable regulatory standards and guidelines. Administer, assess and approve quality documentation, including Incident Reports, Change Controls and Risk Assessments. Conduct data review and internal audits to verify GMP compliance and identify areas for improvement. Evaluate and approve suppliers and service providers, supporting audits of critical suppliers when necessary. Assist QA management with customer audits and regulatory inspections. Deliver training on quality related topics to employees across RoslinCT. Compile quality metrics to facilitate monitoring of the RoslinCT Quality Management System (QMS). About you Comprehensive understanding of cGMP principles. Proficient in computer systems, including Microsoft Office and electronic quality management systems. Strong verbal communication skills, demonstrating confidence when engaging with team members, RoslinCT employees and clients. Excellent written communication skills, with the capability of recording and reporting data clearly, concisely and in compliance with documented procedures. Sound decision-making skills, balancing customer needs with compliance requirements and exercising sound judgement in challenging situations. Proactive in driving continuous improvement, contributing to the enhancement of quality systems and practices. Flexible and adaptable, able to respond positively to both immediate priorities and longer-term planned workloads. Self-motivated and reliable, demonstrating the ability to work effectively with minimal supervision. Qualifications Degree in a Life Science, or related subject or at least 2 years’ minimum industry experience. Next Steps If this sounds like you, then please hit ‘Apply’ now. We will ask you to upload your CV and complete a short application form detailing why you are interested and why we should hire you. 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 jobs@roslinct.com. We’re here to assist and make things as smooth as possible for you.

Responsibilities

The Quality Assurance Officer II will be responsible for writing, reviewing, and updating Standard Operating Procedures (SOPs) to ensure alignment with regulatory standards and company policies. Key duties include administering and approving quality documentation, conducting data reviews and internal audits to verify GMP compliance, and assisting with customer audits and regulatory inspections.