Quality Control Supervisor

3 weeks ago

Edinburgh, United Kingdom RoslinCT Full time

**Quality Control Supervisor - Analytical**

**Location**: Edinburgh BioQuarter, Little France

**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 Control Supervisor - Analytical** to join our team.
- Lead and co-ordinate efforts of our QC Analytical Team in the delivery of QC programmes to the highest standards.
- Lead your team, being responsible for fostering a professional, inclusive, and supportive team environment.
- Schedule analytical activities within the department and ensure all sampling and testing is performed against set specifications.
- Develop and continually improve the awareness of your team in GMP and best analytical practices.
- Review QC procedures to ensure compliance with regulatory standards and identify areas of improvement.
- Review, approval, and co-ordination of QC documentation within the Quality Management System.
- Ensure incidents and changes are documented and approved in accordance with procedures.
- Partner with QC management, MSAT, Development, and Project Management teams in technical and operational discussions, playing an active role in shaping our growing company.
- Co-ordinate outsourced testing and liaise with external testing providers.

**About you**
- Extensive experience in a QC Analytical laboratory.
- A clear understanding of GMP and Quality Control.
- Significant experience in GMP QC analytical assays and testing, primarily flow cytometry and/or qPCR.
- Demonstrable leadership, communication, interpersonal, and motivation skills.
- Excellent decision-making skills and the ability to analyse information in a logical manner and to prepare coherent investigative and/or technical reports.
- A passion for people and teamwork.
- A keenness to learn, educate, and promote best practices in QC.
- Competent in reporting and presenting internally and externally.
- Good IT skills with experience of using Microsoft Office and an electronic quality management system.

**Qualifications**

**Next Steps

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