Quality Control Supervisor

2 weeks ago


Edinburgh, 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 coordinate 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 coordination 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.
  • Coordinate 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 decisionmaking 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
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