Careers

Southern Implants is looking to offer internship positions in the Sales Engineering Department. This 6-month internship is intended for newly qualified biomedical or mechanical engineers who are seeking to obtain exposure in the biomedical industry.

As an intern in this program, the benefits of completing this internship include the following:

• Exposure to different roles and opportunities within a multi-national medical device manufacturing company.
• Development of industry applicable skills under the supervision of experienced biomedical/mechanical engineers.
• Networking within the biomedical industry, both locally and internationally with suppliers, regulatory bodies, industry experts and clinicians.

For Southern Implants, we would hope to gain the following from our interns:

• Skills and knowledge transfer to the company on the latest academic teachings and research.
• Innovative ideas and perspectives.
• Expansion of our talent pool.

This will be a position based at our head office in Irene, Gauteng.

MINIMUM REQUIREMENTS

• BEng or BSc in Engineering with completed or in the process of completing a Master’s in Biomedical Engineering.
• Competent in SolidWorks modelling, simulations, and technical drawings
• Computer literacy (MS-Office)
• Familiarity with a regulatory orientated or high-quality assurance type industry
• Report writing
• Medical Device Design Experience
• Manufacturing Experience
• Computer Programming

Interested applicants meeting the minimum requirements are welcome to submit their CV and cover letter with motivation for why they would be an strong candidate for the 6-month Biomedical Engineering Internship to:  careers.hq@southernimplants.com.

Please ensure the subject header of the email is ‘Biomedical Internship’.

For more information please click here.

Company Description

Southern Implants, established in 1987 and headquartered in South Africa, is a global leader in innovative dental implant products, catering to high-level professional users who seek diverse choices. Renowned for its expertise in research, development, and manufacturing, Southern Implants delivers innovative treatment solutions aimed at reducing treatment time and enhancing patient outcomes. The company’s extensive global network of dedicated representatives provides excellent technical support, allowing clinicians to maintain the highest standards of patient care. Southern Implants continuously expands its product range to incorporate the latest technologies and trends, empowering professionals with innovative solutions to everyday challenges.

Role Description

This is a full-time, on-site role located in Pretoria for a Regulatory Affairs & Quality (RAQ) Associate. The RAQ Associate is responsible for coordinating, preparing, and submitting regulatory documentation to support product registrations and approvals. The role includes ensuring adherence to regulatory compliance and requirements, maintaining quality documentation, and supporting audits and inspections. The associate will also collaborate with internal teams to ensure regulatory alignment across global markets and assist in updating processes for continuous improvement.

Responsibilities

• Develop a strong working knowledge of ISO 13485, MDSAP, and Southern Implants’ Quality Assurance Policies
• Draft, review, and update work instructions, SOPs, and controlled documents
• Maintain effective document control within the QMS
• Assist with Risk Management and Management Review preparation
• Support annual quality and compliance schedules
• Assist with local and international product registrations
• Prepare for and support internal and external audits
• Conduct quality event investigations, non-conformance reports, and CAPAs
• Assist with process and equipment validations
• Support company events such as factory tours and SICON
• Assist with periodic stock counts

Qualifications & Competencies

• Honours Degree in Life Sciences, Engineering, or a related field; OR
• Bachelor’s Degree with relevant work experience
• Advanced proficiency in English, including strong reading, writing, and comprehension abilities.
• Strong attention to detail and documentation skills
• Good analytical and problem-solving ability
• Strong administrative and organisational skills
• High integrity and accountability
• Ability to work independently and within a team
• Strong written and verbal communication skills
• Deadline-driven and structured
• MS-Office competency

Interested applicants meeting the minimum requirements are welcome to submit their CV and cover letter with motivation for why they would be an strong candidate for the role to:  careers.hq@southernimplants.com.

Please ensure the subject header of the email is ‘Regulatory Affairs & Quality (RAQ) Associate’.