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Job Details Posted By : Admin

Refrence No. :#37002119
Location : London
Employer Name :Hays Specialist Recruitment Limited
Duration: Full Time
Posted On :Jan 10, 2019
Expire On :Feb 21, 2019
Pay Criteria : £18.00 - £23.00 per hour
Pay Range: Per Hour

Job Description

QA, Quality Assurance, non-sterile, QMS, Batch Release, Quality Specialist, Quality Documentation, CAPA

Your new company

This national institution is world renowned for its quality of services within the healthcare and medical sector. Their long history of service across multiple disciplines makes them an incredibly reputable company, rich in experience and expertise from an incredibly diverse range of professionals. They have an unwavering commitment to their client base that is reflected within their willingness to evolve and adapt with ever changing socio-political and economic climates.

Your new role

Their London based site is in search of a Quality Assurance Specialist with experience in non-steriles to join their broader team of Quality experts. As a new member of the team, you will be responsible for maintaining Quality Systems relating to ML(Specials) and MA(IMP) licenses as well as internal company standards. You will be required to act as a Releasing Officer under GMP standards in a non-sterile environment, leasing with senior Quality Management and Qualified Person(s) Regularly. Much of the role will involve batch release of medicinal products. Furthermore, the ability to support staff out of the QA department will be essential. The role will also demand the ability to conduct internal audits to regulatory standards as well as compile relevant documentation whilst maintaining the documentation control system.

What you'll need to succeed

A degree in a relevant scientific discipline (such as Pharmacy, Chemistry, or Biology) is essential to the nature of the role and would ideally be supported by a post graduate qualification relevant to pharmaceutical manufacturing. Prior experience for licensed pharmaceutical production, particularly in non-sterile environments, is a must and would do well to be complemented by demonstrated evidence of training or managerial responsibilities. Furthermore, great attention to detail and capacity to monitor risks and take initiative to improve quality processes would be hugely valued.

What you need to do now
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