Associate Clinical Program Supply Chain - Macclesfield, United Kingdom - Cpl Life Sciences

Cpl Life Sciences

Verified Company

Macclesfield, United Kingdom

2 weeks ago

Posted by:

Tom O´Connor

beBee Recruiter

Description

Contract - Associate Clinical Program Supply Chain

We have an exciting opportunity for an
Associate in Clinical Program Supply Chain The
Associate in Clinical Supply Program is a key role in delivering and managing the performance against the overall supply chain strategy.

Working alongside the Clinical Supply Chain Programme Lead to be accountable for parts of the end to end clinical supply.

You will have a specific responsibility either for an aspect within a programme or across several programmes in the portfolio.

This role is based in
Macclesfield, UK or
Gothenburg, Sweden.

Pharmaceutical Technology and Development (PT&D) are the bridge which turns forward-thinking science into actual medicines that help millions of people. We work across the entire value chain, crafting and delivering activeingredients, formulations and devices required to support new medicines - from supplies for use in early toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture.

What you'll do
Manage and contribute to supply chain performance through key performance indicators:

Work in conjunction with the programme lead and
Be responsible for the execution and performance of clinical supply chains contributing to the E2E supply of products in the development portfolio
Own a part of the programme supply chain strategy
Contribute/ Deputise for the programme lead in the Supply Chain Team (SCT) which is accountable for developing and maintaining the supply plan for the project
Work in conjunction with the Supply Chain Planner to balance short to midterm Supply and Demand, Inventory Management and input into D&OP Process
Understand GMP (Good Manufacturing Practice) and the impact it has on supply chain activities
Monitor the performance of the Supply Chain and the make test release processes
Ensure timely delivery of information to meet internal and external regulatory and legal requirements
Manage change in demand and supply within the SC systems, contribute to resolving issues and escalate as required
Be responsible for data management, cost / budget management and reporting process aspects on behalf of the programme group

Essential for the role

Extensive experience of working in supply chains

- experience of business relationship management

Knowledge of Supply Chains, Pharma FMCG, manufacturing
Awareness of GXP Standards within a Clinical environment
Demand Management and forecasting experience
Project Management, change management and risk management capability

Desirable for the role

Technical skills and mindset in supply chain management including demand management, supply chain design, optimisation and delivery
Experience of leading global cross functional teams
Capability in partnering, influencing and optimising customer requirements
Good influencing, negotiating and problemsolving skills, including across functional, geographical and cultural boundaries
Solid understanding of the Clinical Trial Directive and global regulatory environment impacting the provision of investigational products