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Supply Chain Associate

TN United Kingdom

Livingston

On-site

GBP 25,000 - 35,000

Full time

12 days ago

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Job summary

Join a pioneering organization in cell and gene therapy as a Supply Chain Associate. This exciting role involves managing raw materials for GMP manufacture, ensuring compliance with industry standards, and supporting logistics operations. You will play a key role in a collaborative team dedicated to creating life-changing therapies. With a focus on professional growth, the company offers a supportive environment and a competitive salary package. If you're passionate about making a difference in healthcare and have the required skills, this opportunity is perfect for you.

Benefits

31 days annual leave
Competitive pension scheme
Private healthcare
Flexible benefits
Group Life Cover

Qualifications

  • Experience in handling temperature sensitive materials.
  • Competency in inventory management within a GMP environment.

Responsibilities

  • Support Supply Chain and Manufacturing teams with raw material management.
  • Drive a Luton van for material transfer between sites.
  • Ensure compliance with GMP and standard operating procedures.

Skills

GMP experience
Inventory management
Interpersonal skills
Time management
Microsoft Office

Job description

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RoslinCT is a global CDMO focused on Advanced Cell and Gene Therapies. It was established in 2006, built upon the ground-breaking cloning technology of Dolly the Sheep. RoslinCT is one of the first to produce clinical-grade human pluripotent stem cells and developed the first CRISPR-edited cell therapy product for a major inherited disorder, taking it from early development to commercialization.

Supply Chain Associate

Location:This role is primarily based in our BioStore site in Livingstonhowever there may be a requirement to travel to some of our Edinburgh sites.

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!

  • 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.
  • An exciting opportunity for a Supply Chain Associate to join our growing Supply Chain & Logistics function!
  • This position will be responsible for providing support to the Supply Chain, Manufacturing, Cell and Gene Therapy Development and Quality Control teams regarding the management of raw materials procured in support of GMP manufacture and suppliers, planning, and logistics and distribution.
  • You will be required to drive a Luton van to transfer materials between sites, therefore a full clean UK driving licence is required.
  • Assist with material procurement from approved GMP suppliers.
  • Receive inbound deliveries of materials, including ambient, 2-8c and frozen material and move to appropriate holding location awaiting release.
  • Ensure that receipted materials conform to that specified on the purchase order and internal specifications.
  • Inform Quality Control of material that is required to be released and ensure they are released within a timely manner.
  • Liaise with Suppliers to ensure all required documentation/certificates for receipted materials are available when required.
  • Operate first in first out (FIFO) policy and first expired (FEFO) for raw materials and consumables.
  • Assist with the management of appropriate stock levels of all general consumables and carry out stock checks of consumables and reagents with support from the Supply Chain Officer and Co-Ordinators.
  • Replenish materials as required via the inventory management process, ensuring stock is available for production areas.
  • Assist in passing additional materials or paperwork as required to the production team during processing.
  • Assist in shipping temperate sensitive products to clinical trial sites in accordance with Good Distribution Practice.
  • Communicate with internal and external customers to ensure the smooth flow of our CMO services.
  • Perform all activities in accordance with GMP and standard operating procedures.
  • Assist as required with the investigation of supplier complaints.
  • Ensure all materials and equipment is stored safely, correctly, and securely depending on item classifications.

About you

  • GMP experience, preferably within a pharmaceutical environment.
  • A full clean, UK driving licence.
  • For business insurance purposes, the successful candidate must be over the age of 25.
  • Experience of handling temperature sensitive materials.
  • Materials/Inventory management experience in a GMP manufacturing environment.
  • Competency in computer packages including Microsoft Office.
  • Excellent interpersonal skills with the ability to partner effectively with colleagues across the organisation.
  • Exceptional organisation and time management skills.

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 [emailprotected] . We’re here to assist and make things as smooth as possible for you.

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