220 Engineering Certification jobs in South Africa

Duties

Requirements

• U.S. Citizenship Required
• Telework may be authorized.
• If authorized, PCS will be paid IAW JTR and AF Regulations. If receiving an authorized PCS, you may be subject to completing/signing a CONUS agreement. More information on PCS requirements may be found at: PCS Information .
• Security clearance requirements are based upon the actual position being filled.
• Locations are not negotiable. The actual duty locations available may be located on the Air Force Civilian Service website.
• Random drug testing may be required depending upon the position being filled.
• Supervisory requirements may be required depending upon the position being filled.
• Promotion potential may be authorized depending upon the position being filled.
• Full/part-time employees occupying direct childcare positions are eligible for discounts IAW DAF AFSVC/CC Memo, 30 Sep 22; first child 100% / each additional child 25%. Other assigned CYP and FCC personnel are eligible for a 25% discount.

Qualifications

Additional Information

Please note: Positions in this field/series may or may not be available, depending on current manning. For the most up-to-date notifications on available positions, we recommend candidates subscribe and complete their profile.

Eligibility for benefits depends on the type of position you hold and whether your position is full-time, part-time, or intermittent. Contact the hiring agency for more information on the specific benefits offered.

The Quality Assurance Director will provide compliance leadership and direction to our Company and contract manufacturing operation (CMO) sites that manufacture active pharmaceutical ingredients (API), biologics, vaccine drug substances and finished products. As Director, you will support Quality audits and health authority inspections and ensure any resulting corrective and preventative actions (CAPA) are effectively implemented.

Primary Activities

• Serve as a subject matter expert for current good manufacturing practice (CGMP) requirements for vaccine and large molecule manufacturing
• Partner with our Company and CMO management to identify appropriate CAPA to address findings identified during audits and inspections. Monitor CAPA status and ensure CAPA are implemented in accordance with commitments. Perform independent verification of CAPA implementation and effectiveness to ensure no recurrence of findings
• Gather regulatory intelligence and partner with our Company and CMO management to prepare sites for audits and inspections. Assists sites during audits and inspections to ensure successful outcomes
• Monitor and analyze the outcomes of audits and inspections to identify, investigate, and resolve trends. Report results to Divisional and Regional Quality / Management councils
• Provide guidance and consultation services for regulatory reporting (e.g., BPDR, DPR)
• Author and / or review global standards and procedures related to biologics, vaccines, and finished product ensuring compliance with regulatory requirements
• Actively participate in industry organizations such as PDA, PQRI, PhRMA, ISPE, etc.

Education and Required Experience :

• Bachelors degree in Life Sciences, Chemistry, Engineering or related relevant discipline and 10+ years of demonstrated experience within Quality compliance within large molecule manufacturing industry
• Expert knowledge of GMP requirements for multiple regulatory agencies
• Expert knowledge of large molecule manufacturing processes (for biologics and / or vaccines) and sterility assurance requirements
• Ability to accurately interpret and apply regulatory expectations for a robust and compliant QMS
• Experience in health authority inspections

Required Skills :

• Drive Results – set clear performance standards, overcome obstacles; accountable for actions and achieve results
• Make Rapid, Disciplined Decisions – demonstrates good judgment in collecting and synthesizing relevant data and information to make independent and timely decisions
• Act with Courage and Candor – ability and willingness to advocate for compliance position using objective evidence, escalates issues and decisions, as appropriate
• Foster Collaboration – ability to influence, facilitate groups with diverse perspectives, bring teams to consensus / alignment
• Make Rapid, Disciplined Decisions – demonstrates good judgment in collecting and synthesizing relevant data and information to make independent and timely decisions
• Act with Courage and Candor – ability and willingness to advocate for compliance position using objective evidence, escalates issues and decisions, as appropriate

Preferred Skills / Experience :

• Experience working for a health authority as an inspector, investigator, compliance officer, reviewer, or assessor
• Experience creating or assessing remediation plans

EBRG

Current Employees apply

US and Puerto Rico Residents Only :

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit :

EEOC Know Your Rights

EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

U.S. Hybrid Work Model

Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.

The salary range for this role is

169,700.00 - $267,200.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at p>

You can apply for this role through a>

or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

San Francisco Residents Only : We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only : We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status : Regular

Relocation : No relocation

VISA Sponsorship :

Travel Requirements :

Flexible Work Arrangements :

Remote

Shift : 1st - Day

Valid Driving License :

N / A

Required Skills :

Biological Sciences, Biologics, Biopharmaceutics, Corrective and Preventive Action (CAPA), Detail-Oriented, Driving Continuous Improvement, GMP Compliance, Manufacturing, Pharmaceutical Quality Control (QC), Preventive Action, Quality Assurance (QA), Quality Assurance Auditing, Quality Assurance Inspection, Quality Control Inspection, Quality Management, Quality Management Systems (QMS), Quality Metrics, Regulatory Compliance, Regulatory Inspections, Vaccine Manufacturing

Preferred Skills :

Quality Control Reviews, Remediation Plans

Job Posting End Date :

07 / 27 / 2025

• A job posting is effective until 11 : 59 : 59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Requisition ID : R355668

Quality Assurance • Midrand, Gauteng, South Africa

Get AI-powered advice on this job and more exclusive features.

Are you passionate about software quality and testing? Do you thrive in collaborative, fast-paced environments where innovation and precision matter? Softsure is seeking a Quality Assurance Technician to join our growing team based in the beautiful city of George, South Africa.

Your Mission

As a QA Technician, you'll contribute to delivering high-quality software solutions that delight users and support our global insurance partners. We're looking for someone who brings a strong work ethic, attention to detail, and a hunger to learn. At Softsure, you’ll be part of a collaborative, high-performing team where your input makes a real difference.

• Seniority level Entry level

• Employment type Full-time

• Job function Quality Assurance
• Industries Insurance

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QUALITY AND FOOD SAFETY ASSURANCE MANAGEMENT

MANAGEMENT SYSTEM

• Establish, document, implement and maintain a Food safety Management System.
• Define the Scope of the Food safety Management System and specify the products or product categories, processes.
• Ensure that expected Food safety hazards are identified, evaluated and controlled.
• Manage communication throughout the food chain regarding safety issues, development, and implementation and updating of the food safety management system.
• Evaluate periodically and update when necessary, the food safety management system to ensure that the system reflects all activities and the most recent information on the food safety hazards subject to control.
• Manage control over any outsourced processes that affect product conformity with requirements
• Manage documentation requirements, control of documents and control of records.

MANAGEMENT RESPONSIBILITY

• Manage the Management Commitment to Food Safety management System
• Define, document and communicate the Food Safety Policy
• Ensure that the Food Safety Policy is supported by measurable objectives
• Food safety Management System Planning
• Manage Responsibility and Authority
• Food Safety Team Leadership, to report to the Top Management on the effectiveness and suitability of the Food safety Management System
• Manage Internal and External Communication
• Establish, implement and maintain procedures to manage potential emergency situations and accidents that can impact Food Safety and which are relevant- Emergency Preparedness and Response
• Review the Food safety Management System at Planned Intervals, to ensure continuity, adequacy and effectiveness.
• Assess Opportunities for improvements and the need for the changes to the Food safety Management System.
• Maintain Records from management reviews ( Reviews Inputs and Review Outputs )

RESOURCE MANAGEMENT

• Manage Competence, Awareness and Training.
• Ensure that the personnel responsible for monitoring, correction and corrective actions of Food Safety Management System are trained.
• Ensure that the requirement for effective communication is understood by all personnel whose activities have an impact on Food Safety.
• Manage the provision of the resources for the establishment and maintenance of the infrastructure needed to implement the requirements of this international standard.

PLANNING AND REALISATION OF SAFE PRODUCTS

• Plan and Develop processes needed for the realisation of safe products.
• Implement, operate and ensure the effectiveness of the planned activities and changes to the activities include Pre requisite Programme and A HACCP Plan
• Manage the approval of all relevant or updated PRP(s) by the Food Safety Committee
• Identify statutory and regulatory requirements related to the PRP(s)
• Manage verification of planned PRP(s) and PRP(s) modifications
• Maintain Records of verification and modifications
• Manage preliminary steps to enable hazard analysis
• Manage the formally appointment of the Food Safety Committee
• Manage the characteristics of end products and processing records
• Manage, prepare and update Flow Diagrams for products or process categories covered by the Food safety management system
• Manage the verification and accuracy of Process Flow Diagrams
• Maintain verified Flow diagrams in actual HACCP studies conducted
• Manage Hazard Analysis, Hazard Assessment and Selection and assessment of control measures
• Manage the establishment of the operational prerequisite programmes (PRPs)
• Manage the establishment of the HACCP PLAN/CCP Control Chart
• Manage the updating of preliminary information and documents specifying the PRPs and the HACCP Plan
• Manage Verification Planning, Traceability System and Control of Non Conformity (Corrections and Corrective Actions )
• Manage the Handling of potentially unsafe products (Evaluation for releases, disposition of nonconforming products and Withdrawal Evaluation for release)

VALIDATION, VERIFICATION AND IMPROVEMENT OF THE FOOD SAFETY MANAGEMENT SYSTEM

• Manage the Validation of Control measure combinations
• Manage the Food safety management system verification (External/Internal Audits)
• Manage the Evaluation of individual verification results
• Manage the Analysis of results of verification activities
• Manage Process Improvements (Continual Improvement and Updating the Food safety management system)

GENERAL MANAGEMENT

• Staff scheduling to take into account labour legislation with minimum overtime
• Management to fill vacancies, as soon as possible after becoming aware of a vacancy
• Identify training needs of staff and feedback through reporting
• Make arrangements for staff to attend formal training
• Manage the conduction of on the job training
• Cross-train and rotate staff in the factory
• Identify continuous performance problems with subordinates and consult for plan of action
• In consultation with management, take disciplinary action against staff for less serious offences such as counselling and verbal warnings
• Manage the Monitoring of time-keeping and absenteeism, in consultation with management, take disciplinary action when required
• Facilitate communication between staff and management
• Conduct new employee orientation to the workplace

KPAs

• Ensure prevention of microbiological, chemical, allergenic and physical contamination of the products produced.
• Establish and maintain standards and procedures for the control and monitoring of all processes that present Food safety Hazards.
• Utilise HACCP and GMP principles to ensure food safety of all products produced.
• Maintain a system of traceability of all products from raw materials used in all production phases to final product delivered.
• Enable recall of any product should such products be identified as potentially unsafe for human consumption.
• Encourage a culture of continuous improvement and HACCP awareness.
• Continuously train employees on HACCP principles.
• Continuously review and improve our food safety management system and support this through formal communication channels, training and audits.
• Identify and evaluate food safety risks using HACCP principles to be able to effectively control the identified food safety risks.
• Ensure that subordinates are adequately resourced in order to carry out their duties diligently.

Education:

• Grade 12
• Degree in Food Science & Technology, Biochemistry/Biotechnology Qualification

Experience:

• Previous experience in a food production environment
• Previous QA Systems Monitoring & Evaluation
• Good computer literacy especially Excel and e-mail
• Previous experience working with Syspro an advantage
• Experience on Overseeing day to day compliance and food safety
• Leading a Food safety Team and Meetings
  • Quality Control analysis
  • Internal Audits
  • SOP documentation

General

• Expected to work over weekends and public holidays
• Expected to work extended hours from time to time
• Expected to be on stand by and to come in to conduct in house Factory Audits during and after/before Shifts

Skills

• Ability to read, write, understand and communicate in English, Good numeracy, Good computer literacy especially Excel and e-mail.
• Excellent Analytical Skills
• Excellent Communication and Leadership skills
• Excellent Troubleshooting and problem solving skills

About the Role : We are looking for a Quality Assurance Engineer with experience in Playwright to help our client build and maintain high-quality software.

In this role, you will work closely with developers, product managers, and designers to ensure our applications are thoroughly tested, stable, and scalable.

If you have a strong attention to detail, a passion for test automation, and experience working in fast-paced tech environments, we'd love to hear from you!

Join to apply for the Quality Assurance Coach role at Hollywoodbets

Join to apply for the Quality Assurance Coach role at Hollywoodbets

Job Description

Being a part of the Hollywoodbets Purple Team is an opportunity to become a part of one of South Africa’s biggest success stories. From humble beginnings in Durban, Hollywoodbets has grown into a powerhouse brand operating across Africa and the United Kingdom. And that’s just the beginning. Our talented Team is on a mission to increase our global footprint, ready to take on any challenge because at Hollywoodbets, not even the sky is the limit. Join our Team and let’s reach for the stars.

Job Description

Being a part of the Hollywoodbets Purple Team is an opportunity to become a part of one of South Africa’s biggest success stories. From humble beginnings in Durban, Hollywoodbets has grown into a powerhouse brand operating across Africa and the United Kingdom. And that’s just the beginning. Our talented Team is on a mission to increase our global footprint, ready to take on any challenge because at Hollywoodbets, not even the sky is the limit. Join our Team and let’s reach for the stars.

We have an amazing opportunity for a Quality Assurance Coach to be based in Umhlanga. Do you think you have what it takes to be our newest Purple Star?

The successful candidate will be responsible for monitoring and evaluating customer interactions to ensure adherence to company policies, quality standards, and service excellence. This role involves assessing contact (email, chat, voice & other) quality, providing feedback to agents, and identifying areas for improvement to enhance overall customer satisfaction

With Hollywoodbets You Will

Innovate and create as part of a like-minded, authentic Team eager to achieve goals.

Embrace challenges and the thrill of working in a vibrant and fast-paced industry.

Grow with our development plans and culture that allows you to further your career.

You Bring

• 1-year Customer Service Experience
• 1-year Quality Assurance Experience.
  
  

• Degree/Diploma in related field.
• Coaching and analysis experience.
  
  

• Ad hoc listening to call recordings in line with QA scorecard to ensure that ratings are accurate
• Monitor and evaluate customer interactions (calls, emails, chats) for quality and adherence to company standards.
• Calibration participation and attending to help align self and others with QA standards.
• Collate QA reports and statistics for the campaigns, highlighting trends and training opportunities.
• Work closely with the contact centre training division to convert training insights into learning and development modules in Moodle.
• Identify trends and effectively alert the respective departmental management team
• Assist in developing and updating quality assurance guidelines and procedures.
• Customer complaints resolution – extraction and evaluation of call recordings based on customer complaints. Conduct root cause analysis.
• Any other ad hoc duties that might be required
  
  

• Strong Quality Focus
• Good coaching ability
• Customer Service Excellence.
• Exceptional reporting skills.
• Attention to detail
  
  

• Seniority level Entry level

• Employment type Full-time

• Job function Management and Manufacturing
• Industries Gambling Facilities and Casinos

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Join to apply for the Quality Assurance Pharmacist role at ExecutivePlacements.com - The JOB Portal

Join to apply for the Quality Assurance Pharmacist role at ExecutivePlacements.com - The JOB Portal

SUMMARY:

VACANCY: QUALITY ASSURANCE PHARMACIST – JOHANNESBURG

Recruiter:

The Recruiters

Job Ref:

BM030725b

Date posted:

Thursday, July 3, 2025

Location:

Johannesburg, South Africa

Salary:

9000

SUMMARY:

VACANCY: QUALITY ASSURANCE PHARMACIST – JOHANNESBURG

POSITION INFO:

Monthly Salary: R75 000 - Competitive, based on experience and qualifications

Location: Johannesburg, Gauteng

Reference: BM030725b

Are you a Quality Assurance professional with a passion for excellence and compliance in the pharmaceutical sector? Our client, a reputable player in the pharmaceutical industry, is seeking a highly skilled Quality Assurance Pharmacist to oversee and manage all aspects of their Quality Management System (QMS).

This is a critical leadership role focused on ensuring GxP compliance, supporting continuous improvement, and instilling a strong quality culture across the business.

• Review, revise, and authorise departmental SOPs
• Manage full QA function including:
• Document control, Site Master File, Quality Manual & Policy
• Validation Master Plan implementation
• Internal & external audits and deviation tracking
• Root Cause Analysis (RCA), CAPAs & Change Control
• Product Quality Reviews and Quality Management Review meetings
• Supplier approvals and quality agreements
• Non-conformances, Out-of-Specification (OOS) investigations, and ADR reporting
• Implementing and monitoring Stability Master Plan and pest control programme
  

• Investigate and resolve product quality complaints
• Ensure full batch traceability for effective recall procedures
  
  

• Proper handling of returned or rejected goods
• Decision-making on re-testing, re-packing, or destruction
  
  

• Conduct third-party audits
• Ensure compliance across storage, transport, packaging, and destruction of medicines
• GMP training and internal audits
• Batch quarantine, sampling, release, and documentation
  
  

• Ensure continuous GxP and SOP training for all departments
• Support a culture of teamwork, accountability, and compliance
  
  

• B.Pharm Degree
• Registered with the South African Pharmacy Council (SAPC)
  
  

• At least 5 years of experience in Quality Assurance
• Proven experience in document control, SOP management, and working with South African regulatory requirements
  
  

• Proficient in cGxP regulations
• Computer literate (MS Office)
• Strong command of English & Afrikaans
• Excellent communication and interpersonal skills
• High attention to detail, ethical, and deadline-driven
• Ability to perform under pressure and collaborate across departments
  
  

• Seniority level Mid-Senior level

• Employment type Full-time

• Job function Health Care Provider
• Industries Advertising Services

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Our client is seeking a skilled and experienced Quality Assurance Manager to join their team within the Meat Processing sector.

Minimum Requirements:

• Matric
• Degree in Microbiology or relevant
• 5+ years experience working in a similar role
• Experience working in an FMCG Production environment, Meat experience advantageous

Should you meet the requirements for this position, please email your CV to (Email Address Removed). You can also contact the team on (Phone Number Removed); or visit our website at (URL Removed)
Correspondence will only be conducted with short-listed candidates, should you not hear from us in 2 weeks, please consider your application unsuccessful.

Desired Skills:

• Manufacturing
• Quality Assurance
• QA management

Desired Work Experience:

• 5 to 10 years

Desired Qualification Level:

• Degree

1 month ago Be among the first 25 applicants

Direct message the job poster from Nampak

An exciting opportunity exists at Nampak Metals-Springs for a Quality Assurance Technologist (QAT). This position reports directly to the Head of Quality Assurance and is graded at Peromnes 08.

Key Responsibilities:

• Ensuring successful statistical control of processes during production in the Ends Plant
• Evaluate statistical results and monitor CpK values for the plant
• Generate accurate and timely weekly and monthly reports
• Ensure divisional standards and processes are in place for the calibration, verification and maintenance of key equipment in the plant
• Ensuring compliance with ISO 9001 and FSSC systems on site
• Participating in preparation of third party quality and food safety audits
• Ensuring food safety verification requirements are met at all times
• Liaise with customers regarding complaints and provide feedback on resolutions
• Act as Plant Quality & Food Safety Pillar Champion
• Ensuring compliance with the Q-Pulse system and divisional procedures
• Provide training on Quality, Food Safety, and Statistical Process Control (SPC) as required
• Ensure compliance with all relevant ISO, business, and customer standards across the plant
• Prepare for and participate in internal and external audits
• Work with Engineering and production to ensure CQ’s are run on nominal
• Ensure correct isolation process followed in out of control situations as per plant procedure
• Apply problem-solving techniques for customer complaints and quality alerts
• Ensure compliance and adherence to specifications on Datalyser

To excel in this role, the ideal candidate should posses:

• A relevant degree or BTech in Food Science, Food Technology, or a related Quality Management qualification
• A Statistical Process Control qualification
• 5 years’ experience in a quality function within a manufacturing environment
• Proficiency in statistical process control and use of related software
• In-depth knowledge of quality and food safety systems and their implementation
• Demonstrate; confidence, good communication skills and a sense of urgency
• Solid computer literacy and skills

• Seniority level Mid-Senior level

• Employment type Full-time

• Job function Quality Assurance
• Industries Packaging and Containers Manufacturing

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Johannesburg, Gauteng, South Africa 1 month ago

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