Labelling Manager - Global Markets
Major Pharmaceutical Company, Office-based in Surrey
12 month Contract
Globally, my client is the world largest research based pharmaceutical company. Established for over 150 years, my client employs approaching 5000 staff on both a contract and permanent basis- and that's just in the UK! Located in the South East, my clients offices are modern and spacious, with ample free parking, onsite restaurant and are within easy reach of mainline BR.
Working across a variety of therapy areas, my client has changes millionsof peoples lives, by assisting the fight against diseases such as Alzheimer's disease and cancer. Product portfolio stretches across animal health, consumer healthcare, generics, nutrition and prescription medicines. They have an active pipeline andare seeking talented candidates to join the regulatory affairs team on a contract basis.
As a Labelling Manager, you will be responsible for overseeing^all labelling projects for assigned products. This will involve acting as a subject matter expert, responding to questions from regulatory agencies relating to labelling. Your project management skills will be put to good use, tracking labelling and^product progress, using the in house tracking system.
The ideal candidate will be a real people person - you will be working closely with both internal departments, stakeholders and regulatory bodies, so excellent communication skills are essential. Although you will be part of a team, my client is seeking candidates who canwork with a good degree of autonomy, and be self sufficient in updating regulatory documents to include PIL and technical leaflets/documentation globally.
Essential Skills & Qualification
A degree in life sciences or pharmacy will provide a good foundation for this post. The successful applicant will also have some experience of working within regulatory affairs, and experience in working specifically with labelling will be advantageous.
SoftwareCompetence: MS Office, MS Project, DOCUMENTUM
Valid Driving License: Not Required
Working Language(s): English
Requirement for Business Travel: Yes - some occasional travel may be required
Flexible Working Hours: No
Employer: Pharmaceutical Company
Employment Type: Agency Contract
Hours: Full time
Contract Term: 12 Months
Location: UK; Office Based access near M25
Plan Start Date: July 2012, Please do not apply if you are unable to meet this start date.
Contract Benefits: Day Rate inclusive of benefits
MS Office, MS Project, DOCUMENTUM, Labelling, Registration, Regulatory Affairs, MAA, CMC, Expert Reports, Clinical Trial Applications, CTA, Dossier, Regulatory Agency,
Assigned Consultant: Kirsty Clark at CSL Recruitment on 01932 234 681
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 countryconcerned 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.