Training Consultant - United Kingdom - Life Science Recruitment

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Tipperary Details Pharmaceutical Consultant RP/RPi

Degree Experience: 7-9

Years Job Type:

Permanent Salary:
Not Disclosed May be suitable for:Qualified Person Pharmaceutical Consultant RP/RPi

Our client a pharmaceutical consulting organisation are currently recruiting for a Pharmaceutical Consultant to join their team on a permanent basis.

This role is based in the UK, the successful candidate must be able to commute to one of the following office Buckinghamshire, Hertfordshire or Cornwall.

It is fully remote with occasional travel to client sites and ability to go to the office when required. Confirm the status of unique identifiers for Prescription Only Medicines (per Commission Delegated Regulation EU 2016/161) if required for parallel import, special clinical need or for introduction
Liaise with customers in relation to their requirements, determine their needs and timelines and manage client projects including the preparation of project proposals and the implementation of Project Plans including timelines and costings
Conduct Quality Audits for Customers in line with the organisations auditing procedures and in line with all Pharmaceutical Regulatory requirements and standards, to highlight deficiencies to the customers and to support (as required) in the remedy of those deficiencies
To advise and support companies in the establishment and improvement of their Quality Systems
To follow-up with existing customers to ensure satisfaction with service
Prepare draft training material for external class-room based courses and for web based e-learning and downloadable training material
To co-deliver / deliver training to clients
3rd Level Qualification in Science or Quality Management
~10 years experience in Quality Assurance or Quality Compliance role – GMP/GDP
~ High level Computer Literacy and competency – Microsoft Office, Microsoft Project.
~ In-depth understanding of regulatory requirements applicable to the Pharmaceutical Industry, and knowledge of the sources of regulatory information (medical devices and cosmetics industries also considered)
~ In-depth understanding of the purpose, objectives and scope of Quality Systems
~ Creation of third party contracts / project agreements
~ Contributing to company programmes or projects
~ Strong Communication Skills – strong business English capability
~ Strong technical writing skills
~ Project Management Skills

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