Quality Auditor : Tqm (Technical) - Centurion

Ampath Trust; Gauteng; On-site; ZAR 250 000 - 350 000; Full time

Job summary

An established industry player is seeking a Quality Auditor to ensure compliance and quality standards in their laboratories. This role involves conducting internal audits, coordinating clinical trial audits, and maintaining client relationships. The ideal candidate will have a strong background in quality control, possess relevant qualifications, and demonstrate excellent attention to detail. Join a dynamic team dedicated to upholding the highest standards in healthcare and contribute to the continuous improvement of laboratory practices. This position offers a unique opportunity to make a significant impact in a reputable organization.

Qualifications

• 3+ years of quality control experience in a laboratory environment.
• HPCSA registration and relevant qualifications are essential.

Responsibilities

• Conduct internal audits for quality compliance in laboratories.
• Maintain client relations and uphold safety and quality standards.

Skills

Attention to detail

Communication skills

Numerical reasoning

Quality management software proficiency

ISO Internal Auditor experience

Education

HPCSA Registration as a Technician / Technologist

Relevant Medical Technician / Medical Technologist qualification

Training in ISO Medical laboratories

Tools

MS Office

Open Office

Adobe Professional

Document Server

OneDrive

Job description

Advert Reference : PJob Title : Quality Auditor : TQM (Technical) - Centurion

Closing Date : 04 / 04

Position Available From : 03-28

Area : Centurion

Actual Place Of Work : Centurion

Position Type : Full-Time

Weekly Hours : 40

Time Conditions : 5 day Work Week (South Africa)

Purpose of Position : Responsible for performing internal audits for the relevant laboratories and departments.

Identify areas for improvement to uphold the quality and compliance of all laboratories.

Requirements :

1. HPCSA Registration as a Technician / Technologist (Required)
2. Relevant Medical Technician / Medical Technologist qualification (Required)
3. Training in ISO Medical laboratories - requirements for quality and competence (Required)
4. 3 years of experience working with Quality Control; accreditation; safety and audit procedures within a laboratory environment
5. 4 years of experience working as a Medical Technician or a Medical Technologist within a laboratory environment
6. Attention to detail and a methodical approach to work to identify nonconformities and areas for improvement
7. Awareness of accreditation requirements for pathology laboratories and support services
8. Computer skills to use computer technology effectively (MS Office, Open Office, Adobe Professional, Document Server, OneDrive and applications)
9. ISO Internal Auditor experience
10. Knowledge of best practices for training staff on quality standards and procedures
11. Knowledge of health and safety regulations applicable to support services
12. Knowledge of relevant healthcare regulations and standards
13. Numerical reasoning skills to perform basic numerical calculations (e.g., additions, subtraction, multiplication, division and percentages)
14. Proficiency in using quality management software and tools
15. Strong communication and interpersonal skills to work collaboratively with colleagues and stakeholders
16. Understanding of QMS principles, practices, and standards (e.g., ISO , ISO )

Key Responsibilities :

1. Coordinate and conduct internal system audits, for on-site or remote audits, for the Ampath laboratories to ensure quality standards are adhered to
2. Coordinate and perform Clinical trial source data audits at regular intervals
3. Maintain good client relations to promote the image of Ampath
4. Monitor safety requirements and quality management to ensure that relevant safety and quality standards are upheld
5. Perform administrative tasks for TQM training and present Tweets to ensure relevant staff competency levels are upheld
6. Perform administrative tasks to ensure correct recording and handling of audit data and departmental documentation
7. Perform SANAS-required administration duties for assessment applications, when required
8. Stay updated with the latest developments in quality management and safety standards

Applicants must have a South African ID or a valid South African work permit.

We do not accept any faxed or emailed CVs.

If we have not contacted you within 14 days, please consider your application unsuccessful.