Quality Assurance & QC Process Specialist
AI summary
Mid-level QA/QC role in Kampala leading quality management for plastic manufacturing. Responsible for QMS, ISO 9001:2015, UNBS and GMP compliance, inspections, defect management, testing and customer quality issues. Full-time position reporting to the General Manager.
- Mid-level role requiring a Bachelor's degree and 3 years experience
- Focus on ISO 9001:2015, UNBS and Good Manufacturing Practices compliance
- Full-time, 8 to 5 working hours in Kampala
- Covers inspections, defect management, RCA, testing and customer complaints
AI job guide
Use this guide to check salary signals, requirements, documents, application steps and safety before you apply.
AI salary guide
Not enough public dataNot enough public salary data is available for this exact role. Before applying, prepare to ask about gross pay, benefits, contract length, probation period, transport and any allowances.
Can you qualify for this role?
- Required3+ years of relevant experienceThe job post includes a minimum experience signal.
- RequiredEducation or certification mentioned in the postThe captured text mentions education, a diploma, certificate, or licence.
- PreferredPractical evidence in internship, finance, Quality AssuranceThe tags and summary point to skills connected with this role.
- RequiredAvailability to work in Not specifiedThe vacancy is associated with this location.
- UnclearComfort with the Full Time contract termsConfirm hours, duration, probation and benefits at the original source.
Documents to prepare
- Likely requiredUpdated CV
- Role specificCover letter or short employer message
- OptionalProfessional references
- Role specificAcademic or professional certificates
- VerifyID or passport only after verifying the employer
Application tips for this job
- Place your strongest Quality Assurance & QC Process Specialist evidence in the first half of your CV.
- In your cover letter or employer message, connect your experience to Sim Packaging Solutions and the role in Not specified.
- Add concrete examples related to internship, finance, Quality Assurance, ideally with measurable outcomes or clear responsibilities.
- Follow the instructions from BrighterMonday Uganda; avoid sending documents to unofficial contacts or copied links.
- Confirm the deadline, interview location and employer contact before sharing personal documents.
- Prepare a polite question about pay, benefits and contract terms for later interview stages.
Source and safety check
- BrighterMonday Uganda
- Original source link available
- Application method is clear
- Deadline not specified
- No major risk signal was detected in the captured text.
Never pay for interviews, shortlisting, medical checks, uniforms, or job placement. Confirm every application at the original source before sharing personal documents. Report suspicious listing.
Interview preparation
- What experience makes you a strong fit for this Quality Assurance & QC Process Specialist role in internship, finance?
- How have you handled responsibilities similar to those in this job post?
- Are you available to work in Not specified under the listed contract or schedule?
- Prepare examples with clear responsibilities, tools used and measurable outcomes.
- Review the source and research Sim Packaging Solutions before the interview.
Ask what the first priorities will be in the role and how success will be measured.
Similar jobs to consider
Use AI to apply better
After confirming the original source, use Career Assistant to check role fit, tailor your CV and prepare a cover letter or employer message.
Original source description
S
Quality Assurance & QC Process Specialist
Sim Packaging Solutions
Quality Control & Assurance
Today
Easy apply
New
Kampala
Full Time
Manufacturing & Warehousing
Confidential
Share link
Share on WhatsApp
Share on LinkedIn
Share on Facebook
Share on Twitter
Share via SMS
Job summary
To lead quality management, ensuring product quality, compliance with standards, and continuous improvement of quality systems. This role is responsible for developing, implementing, and maintaining functional strategies and a robust quality management system to monitor production processes, prevent defects, and comply with ISO 9001:2015, UNBS requirements, and Good Manufacturing Practices.
Min Qualification:
Bachelors
Experience
- Level:
- Mid level
- Length:
- 3 years
- Language Requirement:
- English
- Working Hours:
- Full Time - 8 to 5
- Applicant
- Location:
- Uganda
- Job descriptions &
- ▪ 3–5 years’ relevant experience, preferably in plastics manufacturing.
- ▪ Proven QA/QC and QMS implementation experience.
- ▪
- in audits, CAPA, RCA, complaints, and continuous improvement.
- Key Skills & Attributes
- ▪ Strong QMS, ISO, GMP and regulatory knowledge.
- ▪ Analytical and problem-solving skills.
- ▪ Leadership, communication and stakeholder-management skills.
- ▪ Knowledge of Lean, Kaizen, Six Sigma and operational excellence.
- ▪ Ability to interpret quality/production data and make evidence- based decisions.
- How to Apply:
- All applications will be received and reviewed through the BrighterMonday Portal by clicking on the 'Apply Here' section
- Log In and Apply
- Important safety tips
- Do not make any payment without confirming with the BrighterMonday Customer Support Team.
- If you think this advert is not genuine, please report it via the Report Job link below.
- Report Job
Requirements
Reports to
the General Manager
Function
Quality Assurance
Internal relationships
: All Departments – Manufacturing, Maintenance, Quality, Engineering, Finance, Procurement, Supply Chain, HR, IT, and Stores
External relationships:
Customers, Service providers, Certification Bodies, Regulators
Purpose
To lead quality management, ensuring product quality, compliance with standards, and continuous improvement of quality systems. This role is responsible for developing, implementing, and maintaining functional strategies and a robust quality management system to monitor production processes, prevent defects, and comply with ISO 9001:2015, UNBS requirements, and Good Manufacturing Practices.
Key result areas and
and actions ÷ total requirements/actions assessed 18%
Process & Product Conformity ≥98% Conforming process/product inspections ÷ total inspections conducted 15%
Defect & CAPA Effectiveness ≥95% Quality corrective actions/CAPAs effectively closed within agreed timelines, with no recurrence of major defects 10%
On-Time Quality Testing & Release :≥98% Testing, validation, and product releases completed within approved timelines ÷ total activities due 10%
Customer Quality Complaints: Zero complaints. Valid quality complaints ÷ total customer transactions/dispatches 15%
Audit & Deviation Closure ≥95%: Audit findings, deviations, and agreed actions closed within approved timelines ÷ total actions due 12%
Quality Improvement & Waste Reduction ≥90%: Approved improvement initiatives completed and measurable waste/scrap reduction achieved against baseline. 10%
Quality Reporting Compliance 100%: Quality reports and performance dashboards submitted accurately and within agreed timelines; reports due 10%
Competency Matrix
Core Leadership R.L Technical R.L Core Values R.L
Execution & implementation 5 Quality Management Systems / ISO 5 Collaboration 5
Accountability & ownership 5 GMP & regulatory compliance 5 Integrity 5
Communication & influence 5 Root Cause Analysis & CAPA 5 Teamwork 5
Problem solving 5 Process monitoring & control 5 Attention to detail 5
Planning & organization 5 Quality inspection & testing 5 Innovation 4
Decision-making 5 Lean, Kaizen & Continuous Improvement 5 Accountability 5
Personal Specifications
Category
Responsibilities
- Key result area Operational tasks Technical tasks
- Quality Management Systems & Regulatory Compliance
- ▪ Develop and implement departmental strategies and plans that drive operational efficiency.
- ▪ Maintain effective QA/QC procedures, standards and processes.
- ▪ Ensure adherence to company quality policies and approved standards.
- ▪ Implement and maintain QMS for plastic manufacturing.
- ▪ Ensure compliance with ISO 9001:2015, GMP and UNBS requirements.
- ▪ Conduct internal audits and drive WCM (World Class Manufacturing), Eagle Way and continuous improvement.
- ▪ Maintain audit readiness and coordinate QMS activities.
- Process Monitoring & Inspection
- ▪ Oversee inspection of raw materials, packaging materials, WIP and finished goods.
- ▪ Monitor production processes for deviations and abnormalities.
- ▪ Ensure timely inspection and release of conforming products.
- ▪ Supervise QC inspection, testing and laboratory activities.
- ▪ Monitor critical process parameters and quality trends.
- ▪ Verify conformity to specifications and approved test methods.
- ▪ Conduct physical and technical analysis of materials and products.
- ▪ Identify process variation and recommend corrective action.
- Defect Management& Root Cause Analysis
- Technical teams.
- ▪ Coordinate containment and corrective actions with Production and
- ▪ Conduct RCA using appropriate problem- solving tools.
- ▪ Investigate product/process defects and prevent recurrence.
- ▪ Track closure of quality actions.
- ▪ Develop and monitor CAPA for defects, deviations, complaints, and OOS results.
- ▪ Analyze defect trends and systemic issues.
- Testing,Validation &,Product Quality
- ▪ Coordinate product testing and validation.
- ▪ Ensure testing and release are completed on time.
- ▪ Manage product quality conformance and support customer quality issues.
- ▪ Execute testing for relevant plastic product properties, including dimensions, strength, and colour.
- ▪ Verify products against specifications and applicable standards.
- ▪ Review and analyze laboratory and inspection results.
- Customer & Market Quality Management
- ▪ Coordinate customer/consumer complaint investigations.
- ▪ Ensure timely response and resolution of complaints.
- ▪ Coordinate product recalls and monitor market quality issues.
- ▪ Analyze complaint and return trends.
- ▪ Conduct RCA on customer complaints and market returns.
- ▪ Recommend corrective and preventive actions.
- Audits, Deviations & CAPA Management
- ▪ Coordinate internal and external quality audits.
- ▪ Record findings and agree corrective actions.
- ▪ Follow up on the closure of deviations, change controls, and audit actions.
- ▪ Maintain quality records and audit evidence.
- ▪ Verify CAPA effectiveness and closure.
- ▪ Monitor deviations, OOS results, complaints and recalls.
- ▪ Analyze quality KPIs, defects, yield and recovery costs.
- ▪ Prepare management quality reports.
- Innovation & Continuous Improvement
- ▪ Identify and implement product/process quality improvements.
- ▪ Drive waste, scrap and rework reduction.
- ▪ Support new and existing product improvement.
- ▪ Monitor quality-related cost impacts.
- ▪ Use quality and production data to identify improvement opportunities.
- ▪ Apply Lean, Kaizen, Six Sigma, RCA, and WCM methods.
- ▪ Evaluate cycle-time, material, and waste reduction opportunities.
- Quality Reporting & Performance Management
- ▪ Prepare periodic quality performance reports.
- ▪ Monitor quality KPIs and close performance gaps.
- ▪ Escalate significant quality risks
- ▪ Analyze quality data and trends.
- ▪ Maintain dashboards for defects, scrap, yield, complaints, CAPA, and audits.
- ▪ Recommend data-driven improvement actions.
- Critical KPIs
- KPI Target Measurement Method Weight
- QMS & Regulatory Compliance ≥95% Compliant QMS/regulatory
Education
- ▪ Bachelor’s degree/diploma in Plastics, Chemical Engineering, or a related field.
- ▪ QMS Internal Auditor certification.