Job Description
Position:Medical Devices Quality Assurance Engineer
Company:Medtronic Angola
Location:Luanda, Angola
Experience:5+ years
Education:Bachelor’s degree in Biomedical Engineering or related field
Employment Type:Full-time
Industry:Medical Devices
Department:Quality Assurance
Salary:2,500,000 – 3,500,000 SSP per month
Vacancies:1
Company Overview
Medtronic Angola is a leading global medical technology company dedicated to improving patient outcomes across the African continent. With a strong presence in Luanda, the company combines innovative product development with local market expertise to deliver cutting‑edge medical devices and therapies. As part of Medtronic’s worldwide network, the Angola branch plays a pivotal role in expanding access to high‑quality healthcare solutions, supporting hospitals, clinics, and health ministries throughout the region. The organization prides itself on a culture of integrity, collaboration, and continuous improvement, making it an attractive destination for professionals seeking meaningful impact and career growth.
Job Overview
The Medical Devices Quality Assurance Engineer will be responsible for ensuring that all Medtronic products manufactured, imported, and distributed in Angola meet the highest standards of safety, efficacy, and regulatory compliance. This role involves close collaboration with cross‑functional teams, including R&D, manufacturing, regulatory affairs, and field service, to implement robust quality systems and drive continuous improvement initiatives. The successful candidate will play a critical part in safeguarding patient health while supporting Medtronic’s mission of alleviating disease worldwide. For more information about Medtronic’s global impact, visit https://angolajobsearch.com/.
Key Responsibilities
- Develop, implement, and maintain quality assurance procedures in accordance with ISO 13485 and local regulatory requirements.
- Conduct risk assessments, design validation, and process verification for new and existing medical devices.
- Lead internal and external audits, ensuring corrective actions are documented and resolved promptly.
- Collaborate with suppliers to qualify components and monitor supplier performance.
- Analyze product complaints, adverse events, and field data to identify trends and drive corrective and preventive actions (CAPA).
- Prepare and submit regulatory documentation to ANVISA Angola and other relevant authorities.
- Provide training and mentorship to junior quality staff and cross‑functional teams.
- Maintain comprehensive quality records and generate reports for senior management.
Required Skills
- Strong knowledge of medical device regulations (ISO 13485, IEC 60601, ANVISA guidelines).
- Proficiency in statistical analysis tools and quality management software.
- Excellent problem‑solving abilities and attention to detail.
- Effective communication skills in Portuguese and English.
- Ability to work independently and lead multidisciplinary projects.
- Familiarity with risk management methodologies such as FMEA.
Education
A Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, or a related scientific discipline is required. Advanced certifications such as Certified Quality Engineer (CQE) or Certified Professional in Medical Device Quality (CPMDQ) are highly desirable.
Experience
Candidates must have a minimum of five years of hands‑on experience in quality assurance within the medical device industry, preferably with exposure to both manufacturing and post‑market surveillance activities. Experience working in emerging markets or within Angola’s healthcare ecosystem will be considered an advantage.
Salary
The position offers a competitive salary range of 2,500,000 to 3,500,000 Angolan Kwanza (SSP) per month, commensurate with experience and qualifications. Additional performance‑based bonuses and benefits are part of the total compensation package.
Benefits
- Comprehensive health insurance covering employee and dependents.
- Retirement savings plan with company matching contributions.
- Paid annual leave and statutory holidays.
- Transportation allowance for commuting within Luanda.
- Professional development budget for certifications and conferences.
Training
- Onboarding program covering Medtronic’s quality systems and corporate values.
- Continuous training on regulatory updates, new product launches, and advanced quality tools.
- Leadership development pathways for high‑potential engineers.
Working Environment
Medtronic Angola offers a modern, collaborative workspace located in the heart of Luanda’s business district. Employees benefit from state‑of‑the‑art laboratory facilities, flexible working arrangements, and a supportive team culture that encourages innovation and knowledge sharing. The company’s commitment to diversity and inclusion creates a welcoming environment for professionals from all backgrounds.
Application Process
Interested candidates should submit their updated CV and a cover letter outlining their relevant experience through the Medtronic careers portal. Applications will be reviewed on a rolling basis, and shortlisted candidates will be invited for a virtual interview followed by an on‑site assessment at the Luanda office.
Equal Opportunity Statement
Medtronic Angola 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. Join us and be part of a team that is shaping the future of healthcare in Angola.