Jobs Career Advice Post Job
X

Send this job to a friend

X

Did you notice an error or suspect this job is scam? Tell us.

  • Posted: Jun 17, 2026
    Deadline: Not specified
    • @gmail.com
    • @yahoo.com
    • @outlook.com
  • We partner with clients who look to us for sourcing talent across South Africa & EMEA. We specialize in sourcing outstanding sales talent from entry level to executive level. We collaborate with our clients to source talent across many job functions predominantly sales but also marketing, business analytics, compliance, regulatory, finance and supply cha...
    Read more about this company

     

    QA Officer - Medical Devices I Midrand

    Job Description

    Responsibilities

    SUPERVISION & TEAM MANAGEMENT

    • Provide day-to-day supervision, task allocation, and guidance to QA Team.
    • Review work outputs for quality, accuracy, and timeliness.
    • Provide coaching, performance feedback, and skills development support.
    • Ensure quality tasks are prioritised and deadlines are met.

    QUALITY PROCESS MANAGEMENT

    • Management of Quality Management System Compliance for All Group of Companies in alignment with the requirements of ISO 13485 ensuring deadlines are not missed.
    • Generation of KPI data, Trend analysis data and provision of reports timeously monthly and for Management Review. Follow up with all sites and departments on monthly KPI data metrics. Ensure data is provided as per approved KPI Metrics.

    RISK MANAGEMENT

    • Set Up Process and Risk Files and continuous maintenance and improvement of the system.
    • Analysis of risk and implementation of corrective actions for Quality Management Systems. Support Teams with Product Risk Assessments in accordance with Group policies and procedures, ISO 13485 and statutory and regulatory requirements.
    • Managing the Group Risk Management programs and databases in alignment with ISO 13485 requirements and ensure deadlines are not missed.
    • Trend KPI data and provide report timeously for Management Review.

    VALIDATION

    • Managing and Maintaining Validation Schedules.
    • Generate validation protocols and reports and support departments where applicable.
    • Support in validation activities for areas under responsibility.
    • Follow up with teams until completion of activities.
    • Trend KPI data and provide report timeously for Management Review.

    INTERNAL & EXTERNAL AUDITS

    • Perform allocated internal audits as assigned;
    • Managing the Group and individual site Internal Audit databases in alignment with ISO 13485 requirements and ensure deadlines are not missed.
    • Support departments with investigations and determining root causes of nonconformities and ensure CAPAs process initiated where required;
    • Trend KPI data and provide report timeously for Management Review.
    • Support with External Audits as per allocated actions.

    GENERAL

    • Support with External Audits as per allocated actions.
    • Reviewing and updating of Standard Operating Procedures and Quality Documents.
    • General administrative duties including archiving, filing, issue of Quality Documents
    • Training: Ensure assigned training is completed timeously; Provide training on areas under responsibility.
    • Individual Quality Improvement Projects are assigned on an annual basis are completed in a timeous manner.
    • Identify improvement areas in processes under responsibility.
    • Recalls And Adverse Events: Support in processes where actions are assigned; Follow up on open recalls and Adverse Events and ensure on time closure.
    • RAD CON, NRCS, ICASA License Applications: Support in processes where actions are assigned.
    • Assistance with SAHPRA Applications: Support in processes where actions are assigned.

    Requirements

    Qualifications

    • Matric (Grade 12).
    • Degree: Science/ Medical / Biological/ Technical/ Quality (Preferred).

    Experience required

    • Advanced Computer Skills (MS Office – Word, Excel, Powerpoint, Teams) - Non-Negotiable.
    • 2-5 years working experience in the medical industry – Non-Negotiable.
    • Experience with data collection and trending.
    • Experience with Quality Management Systems ISO 13485 or ISO 9001 or any other ISO standard – Non-Negotiable.
    • Experience with Regulatory Affairs and understanding of regulations – Preferred.

    Capabilities

    • Highly organized, with attention to detail, producing and expecting highly accurate work within allocated timelines.
    • Methodical and logical structure of executing activities.
    • Excellent interpersonal skills.
    • Ability to develop, lead, and maintain an effective action completion.
    • Fluent in English, verbal and written;
    • Ability to operate & communicate at all levels – verbally & in writing.
    • Able to follow and issue verbal and written instructions.
    • Flexible, conscientious approach.
    • Logical approach to good problem solving and solution driven.
    • Positive attitude, Energetic and able to work independently.
    • Follow up skills and ability to be assertive in meeting deadlines.
    • Willingness to learn and someone who has a hunger to grow and make a difference.
    • Ability to work under pressure.

    Benefits

    • Salary: Market Related

    Check how your CV aligns with this job

    Method of Application

    Interested and qualified? Go to Salesworx Recruitment (Pty) Ltd on salesworx.zohorecruit.com to apply

    Build your CV for free. Download in different templates.

  • Send your application

    View All Vacancies at Salesworx Recruitment (Pty) Lt... Back To Home

Career Advice

View All Career Advice
 

Subscribe to Job Alert

 

Join our happy subscribers

 
 
 
Send your application through

GmailGmail YahoomailYahoomail