RoslinCT

QC Incoming Goods Receipt Associate

RoslinCT  •  Livingston, GB (Onsite)  •  1 hour ago
Apply
AI can make mistakes so check important info. Chat history is never stored.

Job Description

QC Incoming Goods Receipt Associate

Location: Biostore, Livingston.

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 QC Incoming Goods Receipt Associate to join our team.

  • You will perform QC release and inspection activities in compliance with cGMP requirements.

  • Conduct sampling of raw materials and components, coordinate shipments to test houses and manage storage.

  • Maintain accurate documentation and records in line with Good Documentation Practice (GDP).

  • Review and update SOPs and documentation related to QC incoming goods, release, and inspection processes.

  • Collaborate with QC and Supply Chain colleagues to prioritise material processing activities.

  • Contribute to investigations and root cause analyses in support of QMS records.

  • Liaise with suppliers to obtain manufacturing certificates (e.g., COC/COA).

About you

· Prior experience in a QC incoming goods receipt / release area role.

  • Strong understanding of GMP and GDP requirements.

  • Solid knowledge of health and safety practices within a warehouse environment.

  • Physically capable of lifting and moving bulk raw materials between areas multiple times per day.

  • Excellent administrative and record-keeping skills, with the ability to communicate clearly and accurately in written English.

  • Highly flexible and organised, with the ability to adapt effectively to short-term demands.

  • Strong communication and interpersonal skills, fostering effective relationships with colleagues and suppliers.

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.

RoslinCT

About RoslinCT

RoslinCT is a leading global contract development and manufacturing services organization (CDMO) focused on Advanced Cell Therapies.

Established in 2005 and built upon the groundbreaking technology cloning of Dolly the Sheep at the Roslin Institute in 1997, RoslinCT has harnessed cutting-edge science to advance the development of human medicines. With a remarkable heritage in the field, the company has achieved significant milestones, including being among the first in the world to produce clinical-grade human pluripotent stem cells and advancing the first CRISPR-edited stem cell-based therapy for a major disease to marketing authorization.

Equipped with 22 purpose-built cGMP cell therapy processing suites in Edinburgh, Scotland, and Hopkinton, Massachusetts, RoslinCT provides innovative process and analytical development, cGMP clinical and commercial manufacturing for a range of cell types for both autologous and allogeneic processes, and cGMP iPSC cell line development, gene editing, and differentiation.

With tailored CDMO solutions, RoslinCT enables partners to efficiently progress from development to commercialization and deliver life-saving Cell and Gene Therapies worldwide. Discover more about our services at www.roslinct.com.

Industry
Biotech & Life Sciences
Company Size
201-500 employees
Headquarters
Edinburgh, GB
Year Founded
2015
Social Media