Regulatory Affairs Senior Specialist

Wipro Technologies; City of Westminster; Remote; GBP 60,000 - 80,000; Full time

Job summary

A leading global technology company is looking for a Labeling Lead with 4-6 years of experience in Pharmaceutical or Medical Devices. This role involves managing the creation and updates of labeling documents, ensuring regulatory compliance, and guiding the labeling team within a remote working environment. The opportunity also offers career growth and access to diverse benefits.

Benefits

Flexible and fully remote work environment

Access to diverse range of benefits

Personal and professional development programs

Qualifications

• 4-6 years of experience in the Pharma or Medical Devices industry.
• Hands-on registration experience with Regulatory affairs.
• Ability to interpret global and local regulatory guidance.

Responsibilities

• Accountability for the creation and updates of labeling documents.
• Guide the labeling team through regulatory compliance.
• Review labeling content for regulatory requirements.

Skills

Project management skills

Excellent written and verbal communication skills

Logical and analytical thinking

Understanding of regulatory guidelines

Job description

Responsibilities and qualifications for the Labeling Lead role.

Responsibilities

• Has overall accountability for the initial creation and relevant updates to labeling documents
• Guiding the labeling team to develop and maintain Core Date sheets, USPI, SmPC and associated Patient Labeling documents along with regulatory authority driven documents such as Core Safety Profile
• The lead needs to be updated with labeling guidelines and regulations pertaining to the development / maintenance of US and EU labeling
• Should be knowledgeable on key labeling requirements worldwide, in order to ensure that CDS updates may be implemented globally. The lead will review the downstream impact of CDS updates on Local Product Documents (LPDs) and ensure that downstream impact on LPDs is considered during Labeling Team discussions
• Provides project management to the Labeling team throughout the entire process, from the decision making to updates in CDS / USPI / SPC
• Act as a reviewer and signatory during review of labeling ensuring that content complies with regulatory requirements
• Facilitate cross-functional and team awareness and understanding of regulatory issues as appropriate
• Contribute to local or global system and process improvements

Qualifications

• 4-6 years of experience in the Pharma or Medical Devices industry
• Significant hands-on registration experience associated with development, maintenance, and commercialization activities within Regulatory affairs
• Understand regulatory implications of product strategy with regards to the product label & assessment
• Ability to interpret and apply global and local regulatory guidance around labeling and associated supportive documentation
• Excellent written and verbal communication skills
• Proven strength in logical, analytical and writing ability
• Demonstrate project management skills and attention to detail
• Good to have skills :
• Proven understanding of the dynamics and purpose of CDS; experiences of review and implications of CDS
• Prior experience with biologicals
• Opportunity to work in a fast-growing company and in a multinational environment for some of the biggest brands in the world.
• Potential for career growth within the organization and the opportunity to build a successful career path.

Benefits

• Flexible and fully remote work environment, allowing you to work from the comfort of your home in any city in Europe.
• Access to a diverse range of benefits.
• Personal and professional development through a variety of training programs covering both hard and soft skills.
• Comprehensive salary package with various components.
• Complex reward and recognition schemes (both non-monetary and monetary options).