Associate Director

4 weeks ago


United Kingdom Hyper Recruitment Solutions Full time

Join a dynamic team in the heart of London, where the fusion of science and innovation meets quality and leadership. An esteemed pharmaceutical company is seeking an Associate Director for Supplier Quality Management (SQM) to steer their SQM strategy and enhance processes, ensuring excellence in global GxP supplier oversight.

As the Associate Director of SQM, you will be the linchpin for maintaining and elevating core SQM systems, educating and collaborating with internal teams, and leading your team towards impeccable execution of SQM activities. Your role will be pivotal in securing agreements with audit firms, evaluating supply chain risks, and representing the company as a core business owner for the SQM program.

This position offers the flexibility of a hybrid work schedule, with four days on-site in London and one day remote, providing a balanced approach to work-life integration.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the Associate Director of SQM will be varied however the key duties and responsibilities are as follows:

1. Lead the SQM team to ensure compliant and on-time execution of SQM activities, such as, but not limited to: global GxP supplier oversight, audit deliverables, supplier change notifications (SCN), damaged defective raw materials (DDRM), SQM system improvements, and monitoring supplier risks.

2. Engage with internal stakeholders and manage supplier relationships to support business operations. Ensure that SQM processes are designed and operating in a way to provide appropriate support in all GxP areas of the company.

3. Establish, maintain, and improve core Supplier Quality Management processes and systems.

4. Monitor and apply metrics to assess vendor performance and drive continuous improvement.

ROLE REQUIREMENTS:

To be successful in your application as the Associate Director of SQM, the following are sought in your profile and past history:

1. A relevant degree qualification in a Scientific or Engineering related discipline is preferred.

2. Proven experience in a regulated pharmaceutical environment with a focus on GxP Audits.

3. Strong technical expertise in Quality Assurance, Manufacturing, and Clinical environments.

4. Willingness to travel up to 30%.



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