Associate Director of Quality

2 days left

Location
Cambridgeshire
Salary
£50000 to £70000 per annum
Posted
20 Oct 2018
Closes
17 Nov 2018
Ref
J563132
Contact
Chris Sowden
Contract Type
Permanent
Hours
Full Time
Hyper Recruitment Solutions are currently looking for an Associate Director of Quality to join a leading Life Science company based in the Cambridgeshire area. As the Associate Director of Quality you will be responsible for developing and implementing a Quality culture and structure to the Quality teams.

KEY DUTIES AND RESPONSIBILITIES:

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

1. You will develop the Quality culture, continually looking to challenge and improve this culture according to regulatory, customer and internal demands. This will involve developing effective Quality Systems to ensure continued compliance.

2. You will provide the various specific QA teams, such as GCP, GLP and GMP with guidance, encouragement and leadership to adhere to regulatory standards as defined by the FDA and MHRA. The role will involve maintaining accreditations across multiple facilities.

3. As the Associate Director of Quality, you will form apart of the senior leadership team, and will play an active role in developing and enhancing the reputation of the business. As part of this, you will benchmark and identify the business against current trends within the industry.

4. It will be your responsibility to coordinate the efforts of the Quality Department and champion the Quality Culture across the business, including guiding other departments on best practice and compliance guidelines.

ROLE REQUIREMENTS:

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

1. Prior management of QA teams within a pharmaceutical or life science business is essential. This can be within GMP, GCP or GLP. Exposure to GxP would be advantageous.

2. Previous experience working alongside regulatory agencies, such as the MHRA/ FDA as a point of contact is essential.

Key Words: Quality Assurance | QA | Quality Management | GCP | GMP | GLP | Quality Systems | Associate Director | Quality Manager | Senior Quality Manager | FDA | MHRA | Compliance | CAPA | CMO | CRO | Quality Event

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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