RS Hunter Career Opportunity, Friday 29, April 2016

At RS Hunter, we believe our clients have the resources, what we do is to galvanise, advice, and partner with our clients to understand the peculiarities of their businesses and then offer the best HRsolutions and strategies that work.Our objective is to focus on creating an overall people driven value through training, expert HR advisory services and value enhancement to our clientsin small business medium sector range while providing support to larger organisations in the areas of recruitment and executive selection

Drug Regulatory Affairs Head

OUR CLIENT

A reputable multinational Pharmaceutical Company in Nigeria is seeking a qualified, experienced and dedicated individual to fill the position of a Drug Regulatory Affairs (DRA) Head.

JOB PROFILE

Efficient management of regulatory matters in the assigned country group, ensuring registration milestones of global and regional/local projects are met and in line with business and functional objectives. Successful maintenance of existing licences. Input to regulatory strategies aligned with commercial and Regional objectives. Regulatory functional excellence, including all compliance related activities are achieved and maintained.

Main Responsibilities and Duties

New registrations and approvals

Licence maintenance

Local /Global Database (or similar) maintenance

DRA Compliance

Packaging materials: owner of local packages

Promotional material validation and approval

Leadership and Management of Direct Reports (where applicable)

Regulatory Intelligence-managing the regulatory environment

Business awareness e.g.: applies business and commercial basic principles to effectively support proposed regulatory strategies and Portfolio plans.

DRA Budget of assigned cluster

Key Performances

Management of Development Portfolio plans with regular and timely communication of performance, and issues. Update of Portfolio development plans, or input into DASA tool.

Achievement of standard and stretch registration milestones/deliverables.

Time to market of new launches with competitive labelling.

Completeness/accuracy of the cluster Standard Requirements and timely communication to HQs on significant changes.

Effective management and proactive communication of emerging regulatory changes with impact to the assigned cluster/countries to respective local and global stakeholders.

Ability to drive and propose changes on regulatory emerging regulations with successful outcome to the Organization.

Successful stakeholder management (internal and external)

Successful people development and talent retention

Adequate budget management and planning

DRA functional excellence and submission strategies

Achievement of Regulatory compliance deliverables as per global target

QUALIFICATION & EXPERIENCE

Doctorate of State in Pharmacy or similar degree in Life Science

English (Fluent), other languages such as French is desired but not mandatory

Minimum of 6 years’ experience in Drug Regulatory Affairs, preferable at al Pharmaceutical Industry or equivalent

Experienced leader proven successful management of people

Excellent communication and negotiation skills

Strong result driven, ability to bring innovative ideas, “think out of the box”

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