Regulatory Affairs Manager Job Vacancy in Abeokuta, Nigeria – Healthcare – Medical Devices

Job Description

Position:Regulatory Affairs Manager

Company:Johnson & Johnson Nigeria

Location:Abeokuta, Nigeria

Experience:5+ years in regulatory affairs within medical device industry

Education:Bachelor’s degree in Pharmacy, Biomedical Engineering, or related field; Master’s preferred

Employment Type:Full-time

Industry:Healthcare – Medical Devices

Department:Regulatory Affairs

Salary:₦2,500,000 – ₦3,500,000 per annum

Vacancies:1

Company Overview

Johnson & Johnson Nigeria is a leading multinational healthcare company with a strong legacy of innovation, quality, and patient‑centric solutions. Operating across pharmaceuticals, consumer health, and medical devices, the company serves millions of Nigerians and contributes to the broader African health ecosystem. With a commitment to sustainable growth, ethical practices, and community impact, Johnson & Johnson Nigeria has established state‑of‑the‑art manufacturing facilities, research collaborations with local universities, and a robust distribution network that reaches both urban and rural markets. The organization’s culture emphasizes diversity, continuous learning, and a collaborative environment where every employee can make a meaningful difference in improving health outcomes. As part of its strategic expansion in the western region, the company is strengthening its regulatory capabilities to ensure compliance with global standards and local regulations, creating exciting career opportunities for professionals passionate about health innovation.

Job Overview

The Regulatory Affairs Manager will lead the development, implementation, and maintenance of regulatory strategies for Johnson & Johnson’s medical device portfolio in Nigeria. This role is pivotal in ensuring that all products meet the requirements of the National Agency for Food and Drug Administration and Control (NAFDAC) as well as international standards such as ISO 13485 and IEC 60601. Reporting to the Head of Global Regulatory Affairs, the manager will collaborate with cross‑functional teams including R&D, Quality Assurance, Marketing, and Legal to facilitate product registrations, post‑market surveillance, and compliance audits. The position offers a unique platform to influence product lifecycle decisions, shape regulatory policies, and contribute to the company’s mission of delivering safe and effective medical devices to patients across Nigeria. For more information about our corporate values and career pathways, visit our website.

Key Responsibilities

• Develop and execute regulatory strategies for new and existing medical device products to achieve timely market entry.
• Prepare, review, and submit comprehensive dossiers to NAFDAC and other relevant authorities, ensuring accuracy and completeness.
• Maintain up‑to‑date knowledge of Nigerian medical device regulations, international standards, and emerging regulatory trends.
• Coordinate with R&D and Quality teams to ensure product design and manufacturing processes comply with regulatory requirements.
• Lead internal audits and support external regulatory inspections, addressing findings and implementing corrective actions.
• Manage post‑market surveillance activities, including adverse event reporting, vigilance, and product recalls if necessary.
• Provide regulatory guidance and training to cross‑functional stakeholders, fostering a culture of compliance.
• Collaborate with global regulatory affairs colleagues to align local strategies with worldwide policies.
• Monitor and interpret changes in legislation, advising senior management on potential business impacts.
• Prepare and maintain regulatory documentation, including technical files, risk assessments, and labeling.

Required Skills

• Strong understanding of Nigerian medical device regulations and international standards (ISO 13485, IEC 60601).
• Excellent written and verbal communication skills for preparing regulatory submissions and interacting with authorities.
• Analytical mindset with the ability to assess complex technical data and translate it into regulatory language.
• Project management expertise, capable of handling multiple submissions simultaneously.
• Proficiency in regulatory software tools and Microsoft Office suite.
• Leadership qualities to mentor junior staff and drive cross‑functional collaboration.
• Attention to detail and a commitment to high‑quality documentation.
• Ability to work under pressure and meet tight deadlines.

Education

A Bachelor’s degree in Pharmacy, Biomedical Engineering, Biomedical Sciences, or a related discipline is required. A Master’s degree or professional certification such as RAC (Regulatory Affairs Certification) is highly desirable and will be considered an advantage during the selection process.

Experience

Minimum of five (5) years of progressive experience in regulatory affairs within the medical device industry, preferably with direct involvement in product registrations in Nigeria and other African markets. Experience with global regulatory submissions and familiarity with NAFDAC processes are essential.

Salary

The compensation package ranges from ₦2,500,000 to ₦3,500,000 per annum, commensurate with experience and qualifications. The package includes performance‑based bonuses, health insurance, pension contributions, and other statutory benefits.

Benefits

• Comprehensive health and medical insurance for employee and dependents.
• Retirement savings plan with employer matching.
• Annual performance bonus and cost‑of‑living adjustments.
• Paid parental and sick leave in line with Nigerian labour law.
• Employee assistance program and wellness initiatives.
• Company‑sponsored transportation allowance for daily commute.

Training

• On‑boarding program covering company policies, regulatory frameworks, and product portfolio.
• Continuous professional development courses, including regulatory updates and leadership workshops.
• Support for external certifications such as RAC, ISO auditor training, and advanced regulatory affairs diplomas.
• Mentorship from senior global regulatory leaders.

Working Environment

Johnson & Johnson Nigeria offers a modern, collaborative workspace in Abeokuta equipped with the latest technology and resources. Employees benefit from a supportive culture that values diversity, inclusion, and work‑life balance. Flexible working arrangements, including remote work options for certain tasks, are available to promote productivity and employee well‑being.

Application Process

Interested candidates should submit their updated CV and a cover letter outlining relevant experience through the online portal on our career site. Applications will be screened by the Talent Acquisition team, followed by an initial telephonic interview, a technical assessment, and a final interview with senior leadership. Successful applicants will be notified within two weeks of the final interview.

Equal Opportunity Statement

Johnson & Johnson Nigeria is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, disability, or veteran status.