Qualified Person

Full Time
Job Sector:
Nursing / Social Care
South Wales
Salary description:
Start Date:
Job Ref:

A key role within a pharmaceutical company as a Qualified Person who will be responsible for a large range of products.

Qualified Person (QP)
North West England

A new position for a QP within a consistently expanding pharmaceutical company based in the NW. They have grown 30% year on year and are again looking to increase both projects taken on board and permanent staff. The role will join a busy quality team and be responsible for signing off batches of products including; solid-dose, liquids, bio-therapeutics, inhalation, as well as others dependent on projects.

You will have direct contact with clients, CMO's and key decision makers and be responsible for:

Overseeing and maintaining the QMS
To review and release batch manufacturing documents to ensure GMP compliance
Audit internally and ensure site is audit ready at all times
To prepare and manage departmental budget and spending
Provide assistance and advice in quality related investigations in accordance to GMPBenefits

5-10% bonus
Exposure a large range of products
Flexible working hoursRequirements:
The successful candidate should have experience either within either the pharmaceutical or biologics industry in a QP role which is accredited either by the EU or UK authorities. Experience working in a manufacturing environment to GMP regulations is compulsory.

If you would like to register your interest for this position and get further information, please use the link provided. Else please email a copy of your CV to Tyler Datlen at (url removed).

If you have a scientific background and this position is not relevant / suitable for you please feel free to get in touch or visit (url removed) to view our other vacancies. SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors. As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

Keywords: GMP, cGMP, ISO 13485, documentation, QA, QAO, SOP, batch documentation, logbook, QMS, quality management systems, master files, audit, document control, quality administrator, quality assurance, archive, medical device, pharmaceutical, biopharmaceuticals, CAPA, non-conformances, QP, Qualified person

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