Supply Chain Associate at RoslinCT

Livingston, Scotland, United Kingdom -

Full Time

Start Date

Immediate

Expiry Date

20 May, 26

Salary

0.0

Posted On

19 Feb, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

GMP experience, Inventory management, Materials handling, Temperature sensitive materials, IT Proficient, Microsoft Office, Organisational skills, Time management, Communication skills, Supplier liaison, FIFO policy, FEFO policy, GDP compliance

Industry

Biotechnology Research

Description

Supply Chain Associate Location: This role is primarily based in our Edinburgh BioQuarter site however there may be a requirement to travel to our BioStore site in 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! 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 Supply Chain Associate to join Supply Chain team. Receiving inbound deliveries of materials, including ambient, 2-8c and frozen material and move to appropriate holding location awaiting release. Informing QC of material that is required to be released and ensure they are released within a timely manner. Building kits for use within our GMP areas in line with production schedules Liaising with Suppliers to ensure all required documentation/certificates for receipted materials are available when required. Operating first in first out (FIFO) policy and first expired (FEFO) for raw materials and consumables. Replenish materials as required via the inventory management process, ensuring stock is available for production areas. Assisting with shipping temperature sensitive products to clinical trial sites in accordance with GDP. About you Prior GMP experience, preferably within a pharmaceutical environment. Experience with inventory/materials management and handling temperature sensitive materials. IT Proficient, particularly with Microsoft Office. Exceptional organisational and time management skills. Excellent communication skills, with the ability to effectively liaise 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.

Responsibilities

The role involves managing inbound deliveries of various temperature-controlled materials, ensuring timely QC release, and building kits for GMP areas according to production schedules. Responsibilities also include liaising with suppliers, maintaining inventory using FIFO/FEFO, and assisting with shipping temperature-sensitive products to clinical sites.