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Director Regulatory Affairs South Africa

Director Regulatory Affairs South Africa

GSKJohannesburg, Gauteng, South Africa
19 days ago
Job description

Hello. Were Haleon. A new world-leading consumer health company. Shaped by all who join us. Together were improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands including Sensodyne Panadol Advil Voltaren Theraflu Otrivin and Centrum through a unique combination of deep human understanding and trusted science. Whats more were achieving it in a company that were in control an environment that were co-creating. And a culture thats uniquely ours. Care to join us. It isnt a question.

With category leading brands such as Sensodyne Voltaren and Centrum built on trusted science and human understanding and combined with our passion knowledge and expertise were uniquely placed to do this and to grow a strong successful business.

This is an exciting time to join us and help shape the future. Its an opportunity to be part of something special.

About the role

Leading all regulatory and market access operations

Key responsibilities

  • Monitor and report on Regulatory changes that impact on South Africa Business operations / opportunities for OTC pharmaceuticals cosmetics food supplements and medical devices; assess and promote compliance with existing and new laws and regulations
  • Advise / develop procedures for time and cost efficient local regulatory compliance
  • Develop regulatory strategies and implementation plans for the preparation submission and acceleration of new products / Innovations
  • Build relationships with relevant government agencies notified bodies local associations
  • Respond to inquiries from regulatory authorities
  • Provide awareness and training to functional groups in the markets as appropriate.
  • Independently prepares documentation and procedures related to responsibilities; continuously looks for process & resource effectiveness and improvement opportunities
  • Establish regulatory priorities or budgets and allocate resources and workloads
  • Manage activities such as audits regulatory agency inspections or product recall
  • Work closely with Haleon local manufacturing site and lead regulatory advice and process
  • Implement team goals or objectives supervise train motivate or guide team members clearly if needed be knowledgeable about each team members job role

Qualifications and skills

Essential

  • A university degree : Faculty of pharmacy or related health sciences
  • 15 years and more regulatory experience
  • Robust knowledge of industry business model & core strategic processes and understanding the value-added role of regulatory in strategic brand / portfolio planning
  • Robust knowledge of healthcare and regulatory environment external environment and competitor pipelines / portfolios and ability to use knowledge to weigh up challenges and risks. more accountability for decision making and for solving complicated situations
  • We have a strong preference to include and grow our population of South African Professionals .
  • Please save a copy of the job description as this may be helpful to refer to once the advert closes.

    Diversity Equity and Inclusion

    At Haleon we embrace our diverse workforce by creating an inclusive environment that celebrates our unique perspectives generates curiosity to create unmatched understanding of each other and promotes fair and equitable outcomes for everyone.

    Were striving to create a climate where we celebrate our diversity in all forms by treating each other with respect listening to different viewpoints supporting our communities and creating a workplace where your authentic self belongs and thrives.

    We believe in an agile working culture for all our roles. If flexibility is important to you we encourage you to explore with our hiring team what the opportunities are.

    Care to join us. Find out what life at Haleon is really like Haleon we embrace our diverse workforce by creating an inclusive environment that celebrates our unique perspectives generates curiosity to create unmatched understanding of each other and promotes fair and equitable outcomes for everyone. Were striving to create a climate where we celebrate our diversity in all forms by treating each other with respect listening to different viewpoints supporting our communities and creating a workplace where your authentic self belongs and thrives. We believe in an agile working culture for all our roles. If flexibility is important to you we encourage you to explore with our hiring team what the opportunities are.

    As you apply we will ask you to share some personal information which is entirely voluntary. We want to have an opportunity to consider a diverse pool of qualified candidates and this information will assist us in meeting that objective and in understanding how well we are doing against our inclusion and diversity ambitions. We would really appreciate it if you could take a few moments to complete it. Rest assured Hiring Managers do not have access to this information and we will treat your information confidentially.

    Haleon is an Equal Opportunity Employer. All qualified applicants will receive equal consideration for employment without regard to race color national origin religion sex pregnancy marital status sexual orientation gender identity / expression age disability genetic information military service covered / protected veteran status or any other federal state or local protected class.

    Accommodation Requests

    If you require a reasonable accommodation or other assistance to apply for a job at Haleon at any stage of the application process please let your recruiter know by providing them with a description of specific accommodations you are requesting. Well provide all reasonable accommodations to support you throughout the recruitment process and treat all information you provide us in confidence.

    Required Experience :

    Director

    Key Skills

    Proofreading,Adobe Acrobat,FDA Regulations,Manufacturing & Controls,Biotechnology,Clinical Trials,Research & Development,GLP,cGMP,Product Development,Chemistry,Writing Skills

    Employment Type : Full-Time

    Experience : years

    Vacancy : 1

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    Director South Africa • Johannesburg, Gauteng, South Africa

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