Global Labelling Manager. Leading Brands
Major Pharmaceutical Company, Office-based in Surrey
12 month++ Day Rate or PAYE Contract
Rate £££
I'm looking for experts in labelling to support a major initiative and help my client's regulatory compliance and standardisation of product labelling for marketed products around the globe. To apply you must be a SME in this area with good geographic knowledge, that way you can advise, mentor and qualify information and ensure the business practice is^leading edge.
Although a contract this role works within an expert UK based HQ team, you'll work with colleagues and learn about global market needs within a first class work environment.
Job Summary
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 team orientated - 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 can work 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.
Supplementary Requirements:
Software Competence: MS Office, MS Project, DOCUMENTUM
Valid Driving License: Not Required, there are free buses to this site
Working Language(s): English
Requirement for Business Travel: Yes - some occasional travel may be required
Flexible Working Hours: Yes, full time but core hours possible
Employment Information:
Employer: Pharmaceutical Company
Employment Type: Agency Contract
Hours: Full time
Contract Term: 12 Months
Location: UK; Office Based access near M25
Plan Start Date: ASAP
Contract Benefits: Day Rate inclusive of benefits
Keywords:
MS Office, MS Project, DOCUMENTUM, Labelling, Registration, Regulatory Affairs, MAA, CMC,^Expert Reports, Clinical Trial Applications, CTA, Dossier, Regulatory Agency,
Assigned Consultant: Matthew Pike at CSL Recruitment on 01932 228 928
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.