For a Biotechnology Company based in Cambridge
My client is a leading Fortune 500, Biotechnology Company. With headquarters in the USA, my client employs over 500 staff in their UK offices, located in Cambridge and Middlesex on both a permanent and contract basis.
A market leader, my client strives to develop products that change people's lives and in the last 30 years have transformed the management of anaemia, inflammation, and cancer. They have a thriving pipeline and are currently very active in recruiting candidates to join the team on a contract basis.
Both UK sites are easily reachable by mainline BR and have excellent road links with ample free car parking.
My client knows they offer a great place to work. Our client understands that each candidate is not the same, and no two roles are either. That's why they permit up to two days working from home per week depending on the role. Moreover, it's a place where you will be more than a contractor- you will be one of the team, and that even means an early Friday finish!
Work with some of the best in the business!
The purpose of the job is to support the production of global submission components and dossiers. This will include the preparation of electronic document archive for migration including but not limited to electronic file naming, mapping document attributes, document classification, electronic file creation, scanning and importing.
Knowledge of document management systems and processes, guides, policies and SOPs. MS office, (Excel), Adobe Acrobat PDF will be essential, as will a knowledge of Pharmaceutical regulatory affair. Good attention to detail and concentration skills essential.
Essential Skills & Qualification
Although you must be able to work under direction, a conscientious approach to tasks is essential for this post and you should have a high level of autonomy. Prior experience of working within Submissions^Publishing is preferred.
Software Competence: MS Office, Insight Publisher, DOCUMENTUM
Valid Driving License: Not Required
Working Language(s): English
Requirement for Business Travel: No
Flexible Working Hours:^To be confirmed
Employer: Pharmaceutical Company
Employment Type: Agency Contract
Hours: Full time
Contract Term: 6 Months
Location: UK; Office Based in Cambridgeshire
Plan Start Date: 2nd July 2012, please do not^apply if you are unable to meet this start date.
Contract Benefits: Day Rate inclusive of benefits
MS Office, Insight, Publisher, DOCUMENTUM, Regulatory Affairs, Dossier, Regulatory Agency, Publishing, Submissions EDMS
Assigned Consultant: Matthew Pike at CSL Recruitment on 01932 234 685
Please feel free to call for a detailed Job Description or additional information
Applications are reviewed within 24hrs; applicants will only receive feedback if they demonstrate the skills the role requires in their application. The role may be remarketed; if you applied for this role previously and were unsuccessful you will not receive a response. We request that non EU Nationals include evidence of right to work in the country^concerned with their application to be considered. Do supply supplementary information on required location, notice period and expected salary/day rate if you are a new candidate.