Quality Director

Location
Wales
Salary
£80000 to £110000 per annum
Posted
26 Mar 2018
Closes
23 Apr 2018
Ref
J5364
Contact
Chris Carey
Contract Type
Permanent
Hours
Full Time
We are currently looking for a Quality Director to join a leading, award-winning pharmaceutical manufacturing company based in South Wales. As the Quality Director you will be responsible for directing and implementing Quality strategies across the business, ensuring compliance with EU, R.o.W and US regulations. You will also assist the company with their commercial growth plans, advising how they can continue to be compliant within these regulations.

KEY DUTIES AND RESPONSIBILITIES:

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

1. You will need to ensure that the site is currently operating within MHRA and FDA regulations and that all quality systems are in compliance with these regulations. You will need to keep updated with changes in regulations and own the development plans of the quality systems.

2. You will work extremely closely with the Senior Leadership Team and will need to have the gravitas and commercial awareness to advise and encourage stakeholders. As the Quality Director, you will advise the senior leadership team on Quality standards and changes to regulations.

3. As the Quality Director, you will take charge of the current Quality Team and will need to show managerial experience. The team will consist of Head's of Quality and QA Officers working in different specialisms. You will need to oversee the Audit plans, manufacturing and procedure Quality whilst ensuring there is adequate QA coverage throughout.

4. You will work closely with the site Qualified Persons (QPs) ensuring batch release schedules are adhered too. Although you are not expected to be a QP for this position, it would be advantageous.

ROLE REQUIREMENTS:

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

1. Prior experience managing a Quality Assurance unit within a Pharmaceutical or Life Science industry. Any experience at executive or board level would be beneficial.

2. Prior experience working and liaising with regulatory bodies, such as the MHRA, FDA is essential. You will be the lead contact with the regulatory bodies, with the aim of positive outcomes.

3. Experience working within a Pharmaceutical or Life Science manufacturing site is highly advantageous. You must have knowledge of working within GMP standards.

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Hyper 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.

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