Serialisation SME and Artwork Co-ordinator
- South East
Elstree
- Permanent
£45000 - £55000 per annum, Benefits: Bonus + Benefits Package
- Life Sciences
01-10-2019
23349
This vacancy has now expired
Do you relish the opportunity to work with a leading UK based Biologics manufacturer? If yes, then this is the position for you!
Our biotech client with manufacturing facilities just outside London, is currently investing significantly in their manufacturing programme. This state-of-the-art facility houses high-technology and next-gen processes to produce drugs that are distributed throughout the Globe. The site is easily reachable by two major airports and has excellent transport links throughout.
The client is currently seeking the expertise of a Serialisation SME and Artwork Coordinator to join their expanding team!
In this role you will be responsible for guaranteeing that the client is compliant with Global serialisations legislations, this will include emerging markets. You will be responsible for maintenance of the serialisations systems ensuring Master Data is correct and active. Along with this you will be tasked with consistently striving to improve the efficiency and effectiveness of the serialisation and artwork creation processes.
You will have the following experience/qualifications:
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Our biotech client with manufacturing facilities just outside London, is currently investing significantly in their manufacturing programme. This state-of-the-art facility houses high-technology and next-gen processes to produce drugs that are distributed throughout the Globe. The site is easily reachable by two major airports and has excellent transport links throughout.
The client is currently seeking the expertise of a Serialisation SME and Artwork Coordinator to join their expanding team!
In this role you will be responsible for guaranteeing that the client is compliant with Global serialisations legislations, this will include emerging markets. You will be responsible for maintenance of the serialisations systems ensuring Master Data is correct and active. Along with this you will be tasked with consistently striving to improve the efficiency and effectiveness of the serialisation and artwork creation processes.
You will have the following experience/qualifications:
- Strong knowledge of current Global Serialisation/ Track and Trace legislation
- Experience in the implementation of serialisation systems
- Demonstrable knowledge of cGMP and other regulatory requirements applicable to the pharmaceutical industry
- Knowledge of requirements for future country specific legislation (Brazil, Russia, China)
- Understanding of the regulated packaging requirements.
To view Quanta's privacy policy, please visit our website
I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Project Director
Global Pharmaceutical firm
Global Pharmaceutical firm
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Engineering Director
Global Pharmaceutical firm
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
Contractor
QA Specialist
QA Specialist
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