Quality Control Supervisor

**Quality Control Supervisor - Analytical**

**Location**: NINE, 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

**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 us as part of our continued growth and success.
- The Quality Control Supervisor will be responsible for coordinating the efforts of the analytical and microbiology teams to deliver the testing/monitoring requirements within the company and manage the resources/personnel available most effectively.
- The main objectives of this role are:

- Lead, manage, and motivate QC personnel to ensure delivery of required work as a team to the highest of standards.
- Ensure that ATMPs and stem cell lines produced by RCT are quality controlled to a standard meeting GMP requirements.
- Co-ordinate and oversee the management of documentation and data required for the activities performed by QC including method validation/transfer, GMP material testing, ATMP batch release and stability testing and environmental monitoring.
- Oversee the conduct of actions associated with quality events in the QMS (Deviations, CAPA, change controls and OOS/OOT events) and ensure timely closure. Participate and/or lead lean initiatives to improve the operations within QC.

**About you**
- You will have significant experience working in a QC laboratory.
- Demonstrate leadership qualities, communication, interpersonal, and motivational skills.
- Able to take decisions, analyse information in a logical manner, and prepare coherent investigative and/or technical reports.
- A clear understanding of GMP and Quality Control.
- Demonstrate competence in reporting and presenting internally/externally.
- A good working knowledge of Good Engineering Practice and process improvement tools such as Six Sigma, Lean processes, and FMEA.
- Demonstrate proficiency with computer software, especially the Microsoft-365 suite.
- You will take responsibility for setting high standards and looking at the bigger picture to recognise the impact of actions.
- You will have excellent written and verbal communication skills with the ability to partner with colleagues across all departments.
- Excellent organisational skills with the ability to multi-task in a fast-paced and dynamic environment.

**Qualifications**

**Next Steps**
- 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._