Regulatory Affairs Specialist
- England, East Anglia
Buckinghamshire
- Contract
Competitive
- Drug Safety / Pharmacovigilance
35688
This vacancy has now expired
Regulatory Affairs Specialist - Pharmaceuticals - 6-Month Contract
Do you want to be part of a forward thinking global pharmaceutical client who have facilities in over 60 countries worldwide? Then this is the next step for you! One of our global pharmaceutical clients is currently requiring an experienced Regulatory Affairs Specialist for their Buckinghamshire based location.
Responsibilities:
Experience/Qualifications:
If this role is of interest to you, please apply now!
#LI-KT1
Do you want to be part of a forward thinking global pharmaceutical client who have facilities in over 60 countries worldwide? Then this is the next step for you! One of our global pharmaceutical clients is currently requiring an experienced Regulatory Affairs Specialist for their Buckinghamshire based location.
Responsibilities:
- Regulatory review and approval of product labelling for Cosmetics and other non-OTC classes per the company portfolio in mainly UK & Ireland
- Regulatory review and approval and advertising or promotional copy for Cosmetics and other non-OTC classes mainly in UK & Ireland
- Support the Regulatory team with specific tasks per the needs of the department, which may include claims tracker updates, databases, compliance tasks
- Work with the regulatory team to develop project implementation plans and manage resource planning to ensure on time completion of projects and tasks
- Project management and implementation of regulatory changes to company assets (product label and promotional materials)
- Work with cross functional partners to drive regulatory strategy and implementation
- Regulatory review and approval of key documents before product ap
- Complete market impact assessments
- Portfolio survey (where used of ingredients)
Experience/Qualifications:
- Minimum B.S. Chemistry, Biology, or related fields
- Significant experience in Cosmetic Regulatory affairs mainly with promotional material and artwork review/approval at all stages of life cycle management, with demonstrated accountability of managing multiple brands.
- Well versed with UK ASA, CAP, BCAP Guidance for Advertising, proven record of successful project management of dossiers with ClearCast
- Strong knowledge and application of the UK & EU Cosmetic Product Regulation
- Excellent leadership, communication, and organisational skills
- Attention to detail, effective in written and oral communication
- Works independently to plan, conduct, and manage regulatory projects to meet department and company objectives
- Responsible for identifying, implementing and managing key RA Departmental projects and/or strategies based on both short- and long-term RA Department objectives.
If this role is of interest to you, please apply now!
#LI-KT1
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing'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 QCS Staffing's people and their ability to deliver.
Engineering Director
Global Pharmaceutical firm
Global Pharmaceutical firm
I have always received a highly professional & personable service from the team at QCS Staffing. 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
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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