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Supplier Quality Manager

CambridgeshirePermanent
Experience Dependant
Job Reference: J5632498
Updated On: 27/11/2019
Status: Now Interviewing
Hyper Recruitment Solutions
Sectors: Pharmaceutical, Medical Device, Contract Manufacturing Organisation, MHRA QP License Holder

Skills: Quality Assurance - Permanent, Quality Assurance - GMP, Quality Assurance - ISO13485, Quality Assurance - Compliance, Quality Assurance - Auditing, Quality Assurance - Quality Manager, Quality Assurance - Clinical Supplies

Job Information

Role Overview

We are currently looking for a Supplier Quality Manager to join a leading Medical Device company based in the Cambridgeshire area. As the Supplier Quality Manager you will be responsible for the build of a number of Quality Systems alongside ensuring Vendor / Supplier compliance.

Key Duties and Responsibilities

Your duties as the Supplier Quality Manager will be varied however the key duties and responsibilities are as follows:

1. As the company scales up to allow them to manufacturer their own portfolio of products, alongside manufacturing products for clients, you will be tasked with designing and implementing GMP compliant laboratories and manufacturing suites.

2. As the Supplier Quality Manager, you will implement the Supplier Quality Assurance program, which will involve the scheduling, planning and conducting of supplier audits. This will include travel to various suppliers across the UK, EU and United States.

3. You will work with the wider business to determine needs and supply strategies. This will be for both new suppliers, which you will asses suitability of, as well as existing suppliers ensuring appropriate Quality and Technical agreements are in place.

4. You will represent the companies Quality team to both customers, suppliers and regulatory bodies. This will include leading and hosting inspections. You will have expert knowledge of the companies QMS.

Role Requirements

To be successful in your application to this exciting opportunity as the Supplier QA Manager we are looking to identify the following on your profile and past history:

1. Previous experience managing and developing a Quality System (QMS) is essential. It would be desirable to have previous experience implementing a new Quality System alongside experience working within a sterile / cleanroom environment.

2. Previous experience auditing to GMP standards is essential. If you have had any previous experience working with Medical Devices and ISO13485, MDD, MDR, then this would also be beneficial.

3. You will have previous experience in Supplier / Vendor management.


Key Words: Quality Assurance | Quality Manager | QMS | Supplier | Vendor | GMP | MDD | MDR | ISO13485 | Audit | Cleanroom | Sterile | Combination | GAMP | Schedule | Compliance

Chris Carey
Your Recruitment ConsultantChris Careychris.carey@hyperec.com
DisclaimerHyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment processionals and scientists. We look forward to helping you with your next career moves.