94 Lab Analyst jobs in South Africa

Overview

Our client, a leader in the food manufacturing industry, is seeking a vibrant, motivated, and adaptable Junior Lab Analyst to join their team as an intern on a 4-month contract.

• Inputting of accurate information into electronic platforms (PowerBI, Entecom)
• Conducting analysis (chemical and microbiological analysis as per SOPS)
• Calibration of instruments when on duty
• Conduct tasks as required by QAC to ensure compliance with BRC standards
• Junior Analyst must ensure that his / her workspace is kept neat and tidy in accordance with the 5S principles

The Senior Lab Analyst is responsible for ensuring that all laboratory testing and analysis are conducted accurately, efficiently, and in compliance with standard operating procedures. This role includes laboratory management, in-process control, training and development, performance monitoring, and ensuring adherence to health, safety, and quality standards.

Key Responsibilities:

Laboratory Management

Responsibilities:

• Ensure that all testing is performed on time and in accordance with set priorities.
• Conduct analysis according to required procedures and document results accurately.
• Ensure complete, signed, and timely submission of documentation.
• Collaborate with other departments to address and resolve quality concerns.
• Perform internal daily calibration and conduct maintenance routines for laboratory instruments.
• Organize and monitor the external calibration of instruments to maintain accuracy.
• Ensure laboratory equipment is in good working condition and conduct preventative maintenance.
• Maintain an adequate stock of consumables to prevent shortages.
• Ensure proper waste management procedures are followed in compliance with regulatory requirements.

In-Process Control

Responsibilities:

• Prepare and standardize volumetric solutions according to procedures and methods.
• Assist in repeat testing and analysis where required.
• Conduct Reverse Osmosis (RO) water testing and determine necessary adjustments to bulk materials in collaboration with the QAQC Manager.
• Perform various chemical and physical analyses as per the Daily Sample Register.
• Coordinate external testing, ensuring timely sample dispatch and result tracking.
• Maintain raw material standards and monitor expiry dates to ensure compliance.

Training and Development

Responsibilities:

• Update, create, and maintain specification sheets, SOPs, and analytical methods.
• Implement and oversee training programs for laboratory staff.
• Supervise and assist trainees, junior technicians, and laboratory personnel.
• Collaborate with the Safety and Security Officer to ensure laboratory safety compliance.

Performance Control and Communication

Responsibilities:

• Investigate Out-of-Specification (OOS) results and initiate NCRs.
• Ensure all SBUs are updated within 24 hours.
• Monitor, document, and report on laboratory team performance monthly.
• Represent the laboratory at SBU meetings and ensure effective communication with relevant stakeholders.

General Duties

Responsibilities:

• Ensure strict adherence to SOPs.
• Ensure compliance with health, safety, and environmental regulations.
• Ensure adherence to company policies and procedures at all times.

Competencies

• Attention to Detail
• Problem-Solving
• Time Management
• Collaboration
• Leadership & Mentorship
• Adaptability

Kindly email applications to

Salary is market related.

Job Types: Full-time, Permanent

Work Location: In person

One of the conditions under the Protection of Personal Information Act 4 of 2013 (POPIA) provides that candidates have the right to be informed about the collection and use of their personal information,

In the course of your application: we may

• collect personal information that may be used to identify potential professional opportunities other

than the job you have applied for but of which we think might be of interest to you.

• use your Personal Information to confirm references or background checks you have provided us.
• request your consent to participate in aptitude tests or recruitment assessments.

We also use your personal information to respond to your inquiries, to verify your information and to share information with you.

Your personal information will be securely stored by the Human Capital Department, and it will be retained for a period of up to 12 months as of the closure of the application procedure if your application is unsuccessful, and in case of a successful application and you are hired, your data will be transferred to your personal employee file.

By applying for this position, you consent to us processing your personal information.

We reserve the right to make an appointment. If you have not heard from us within 30 (thirty) days of the closing date, please accept that your application was unsuccessful. Correspondence will be entered into only with shortlisted candidates

Job Purpose:

This may include analysis of raw material, bulk, imported, finished products and stability samples to ensure compliance to specifications prior to release. Ensure that the scope of practice is met with regard to current Good Laboratory Practice in line with local and international requirements.

Key Job Outputs:

Routine testing as per relevant Test Methods and procedures for Raw Materials, In Process samples, Finished Products, Process Validations, Stability, Post Importation:

• Carry out analysis following the method of analysis and ensuring that technical data generated meets specification and obtain release within the agreed timelines.
• Evaluate data to ensure compliance to release specification.
• Generation of analytical test data reports.
• Conducting investigations required for out of specification results together with supervisor.

Process validation and customer complaints testing (If required):

• Carry out analysis required as per validation protocol.
• Evaluate data to ensure compliance to specification.
• Recording results as per protocol.
• Ensure timeous product complaint analysis as per procedure

Documentation Compiling and Review

• Ensure that all documented activities are in compliance with guidelines and procedures
• Total Quality Management (GMP and GLP): Ensure that scientific integrity of data is maintained
• Review own work to ensure accuracy, completeness and compliance with departmental procedures.
• Ensure that all documented activities are in compliance with guidelines and procedures.

• Report deviations and out of specification results immediately.

• National Diploma/BSc Degree in Chemistry and/or equivalent

• 2 Years Pharmaceutical Laboratory Testing experience (Essential)
• Ability to multi-task
• Ability to think analytically
• Critically Attention to detail
• Good communication skills (spoken and written)
• Strong background in Chemistry and Physics.
• Able to follow instructions and production schedules

Closing Date: 16 September 2025

One of the conditions under the Protection of Personal Information Act 4 of 2013 (POPIA) provides that candidates have the right to be informed about the collection and use of their personal information,

In the course of your application: we may

• collect personal information that may be used to identify potential professional opportunities other

than the job you have applied for but of which we think might be of interest to you.

• use your Personal Information to confirm references or background checks you have provided us.
• request your consent to participate in aptitude tests or recruitment assessments.

We also use your personal information to respond to your inquiries, to verify your information and to share information with you.

Your personal information will be securely stored by the Human Capital Department, and it will be retained for a period of up to 12 months as of the closure of the application procedure if your application is unsuccessful, and in case of a successful application and you are hired, your data will be transferred to your personal employee file.

By applying for this position, you consent to us processing your personal information.

We reserve the right to make an appointment. If you have not heard from us within 30 (thirty) days of the closing date, please accept that your application was unsuccessful. Correspondence will be entered into only with shortlisted candidates

Job Purpose:

This may include analysis of raw material, bulk, imported, finished products and stability samples to ensure compliance to specifications prior to release. Ensure that the scope of practice is met with regard to current Good Laboratory Practice in line with local and international requirements.

Key Job Outputs:

• Ensure compliance to national / international regulatory requirements with respect to Quality Management Systems and current Good Manufacturing Practices (cGMP) within QC laboratory.
• Ensure awareness of cGMP and cGLP among all personnel.
• Ensure all Standard Operating Procedures (SOP's) are updated
• Performing of departmental self-inspections (Monthly).
• Follow up with the lab section managers for closure of CAPA, CCP, OOS and Deviations, and identified Root Cause Analysis and Risk Assessment
• Ensure that all OOS, Deviations raised a, CAPA and CCP are properly documented, investigated and closed according to S.O.P.
• Assisting and ensuring that Annual Product Quality Reviews (APQR) documentation are completed and available for APQR reports.
• Follow up closure of all Internal or External Audit findings by ensuring recommendation are made, and corrective and preventative are identified as results of such audit and are effectively implemented.
• Escalate any critical and major CGMP and CGLP nonconformities found during departmental self-inspection to QC Laboratory Manager.
• Monthly submission of the departmental inspection to QA
• Submission of Internal/External audit finding feedback to QA
• Ensure all Authorized analytical reports are scanned by the LIMS administrators
• Tracking of deviation, CCP, CAPA, OOS, Root cause analysis and Risk assessment with status
• Authorizing of department self-inspection report
• Competence in planning,
• Moderate to High degree of work pressure
• Incumbent must be able to work with no supervision of work detail
• To act in a GMP and GLP compliant manner at all times while carrying out all duties.
• Ensure that training needs and competence are kept up to date in the relevant GMP and GLP topics.
• Study new guideline and policies from regulators to keep abreast with development and changes with regards to legal and regulatory requirements pertaining to pharmaceutical laboratory.
• Authorising of department self-inspection report
• Competence in planning,
• Moderate to High degree of work pressure
• Incumbent must be able to work with no supervision of work detail
• To act in a GMP and GLP compliant manner at all times while carrying out all duties.
• Ensure that training needs and competence are kept up to date in the relevant GMP and GLP topics.

• Study new guideline and policies from regulators to keep abreast with development and changes with regards to legal and regulatory requirements pertaining to pharmaceutical laboratory.

• Analytical Chemistry / Biotechnology Diploma /BSC in Chemistry

• 4 years of Laboratory experience preferable a pharmaceutical laboratory
• Have a good understanding of QMS.
• Broad knowledge of GMP regulations and Good Laboratory Practices
• Knowledge of commonly used analytical laboratory methods as well as knowledge of USP / BP Compendia methods
• Computer Literacy – MS Office (proficient in Excel, Word and Power Point).
• Able to work with people
• Good in Presenting and communicating information
• Good in writing and reporting
• Adapting and responding to change and able to Cope with pressures and setbacks.
• knowledge of auditing will be an advantage.

Closing Date: 16 September 2025

We're Hiring: Quality Control (QC) Consultant

Location:
Johannesburg (Hybrid options available)

Salary:
R16,500 basic (p/m) + incentives

Closing Date:
08 September 2025

At
IPS Health & Wellness
, we're looking for a detail-driven
Quality Control Consultant
to join our dynamic QC team. This is
not a lab or product QC role
– instead, you'll be at the heart of ensuring our customer interactions are professional, compliant, and aligned with our standards.

What you'll do:

• Listen to and analyse call recordings across Sales, Client Care, Lead Generation, and Retentions.
• Provide constructive feedback to consultants and managers to drive performance.
• Verify and enhance QC notes with insights that capture the consultant's perspective.
• Recommend improvements to scripts, compliance adherence, and overall customer experience.

What we're looking for:

• A
  Bachelor's degree (3 years minimum)
  .
• Strong communication skills in
  English and Afrikaans
  (other languages are a plus).
• Someone who is objective, trustworthy, and discreet.
• Analytical thinker with a sharp eye for detail.
• Comfortable with call monitoring and quality assurance tools.
• Organised, innovative, and able to work independently and in a team.
• Knowledge of call centre operations and compliance requirements.

Why join us?

• Work 08:00 – 16:30 with
  flexitime
  available after probation (3 months).
• Remote work
  opportunities based on performance.
• A supportive, growing environment where your feedback directly impacts the customer journey.
• Employment equity principles apply – we strongly encourage applications from designated groups and candidates with disabilities.

We are seeking a Quality Control Lead with expertise in microbiology, environmental monitoring, and biological testing. The role oversees laboratory operations, ensures compliance with regulatory standards, and drives continuous improvement in microbiological quality systems.

Key Responsibilities:

• Lead QC microbiology operations, including sterility testing, microbial identification, and bioburden analysis.
• Oversee environmental monitoring programs for cleanrooms, utilities, and controlled areas.
• Ensure adherence to GMP, GLP, and regulatory requirements (FDA, EMA, WHO, SAHPRA).
• Review and approve test results, protocols, deviations, and CAPAs.
• Train and mentor microbiology analysts, ensuring technical competency and compliance.
• Collaborate with manufacturing, QA, and regulatory teams to support product release and investigations.
• Drive improvements in laboratory practices, data integrity, and contamination control strategies.

Requirements:

• Bachelor's degree or higher in Microbiology, Biotechnology, or related life sciences field.
• 6+ years' experience in pharmaceutical microbiology or biological QC testing, with at least 2 years in a leadership/supervisory role.
• Strong knowledge of GMP regulations, environmental monitoring programs, aseptic techniques, and cleanroom standards.
• Experience with microbial identification systems (e.g., MALDI-TOF, PCR-based methods).
• Proven ability to manage teams, audits, and cross-functional projects.
• Excellent problem-solving and decision-making skills.

Preferred:

• Master's degree in Microbiology or related field.
• Experience with vaccines, biologics, or sterile drug product manufacturing.
• Prior involvement in regulatory inspections.

Job Title: Quality Control (QC) Analyst

Location: Cape Town, Ndabeni

Contract Type: Permanent

About the Role:

Barrs Pharmaceutical Industries (Pty) Ltd is seeking a skilled and experienced Quality Control Analyst to join our Quality team. This role is key in ensuring the highest quality standards for our raw materials, in-process samples, and finished products.

Key Responsibilities:

• Conduct raw material, in-process, stability, and finished product testing.
• Perform analytical and microbiological testing in compliance with SOPs and GMP standards.
• Operate and maintain laboratory equipment including HPLC, density meter, pH meter, potentiometer, Karl Fischer, conductivity meter, and other analytical instruments.
• Prepare, record, and interpret test results accurately and on time.
• Support continuous improvement in QC processes and maintain laboratory documentation.
• Assist in investigations, deviations, and reporting as required.

Qualifications & Experience:

• Tertiary qualification in Chemistry, Biotechnology, Microbiology or a related field.
• 3–4 years' experience as a QC Analyst in the pharmaceutical or manufacturing industry.
• Hands-on experience with raw material testing, analytical chemistry, microbiology, and stability testing.
• Proficiency in operating HPLC and other key analytical equipment.
• Strong knowledge of GMP, GLP, and regulatory compliance.

Key Competencies:

• High attention to detail and accuracy.
• Strong problem-solving and analytical skills.
• Ability to work independently and as part of a team.
• Excellent communication and reporting skills.

How to Apply:

Interested candidates are invited to submit their CV and supporting documents to

Closing date: 19 September 2025

Please note: Only shortlisted candidates will be contacted. Should you not hear from us within 2 weeks after the closing date of applications, please consider your application unsuccessful.