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Join to apply for the QA Compliance Inspectors role at Aspen Pharma Group

Join to apply for the QA Compliance Inspectors role at Aspen Pharma Group

Fine Chemicals Corporation requires the services of QA Compliance Inspectors for our Quality Assurance Department.

Overview

• Responsible for ensuring that all manufacturing activities at the facility comply with current Good Manufacturing Practices (cGMP), regulatory requirements, and internal quality standards.
• To provide oversight of batch documentation, batch release, audit readiness, OTIF (On-Time In-Full) support, and plant floor compliance monitoring.
• Collaborate with production, QC, and engineering teams to ensure GMP compliance and product quality.
• Promote a culture of quality and compliance across operations.
  
  

Responsibilities

• Review and approve Batch Production Records (BPRs), cleaning logs, and associated documentation.
• Ensure completeness, accuracy, and compliance of batch records with regulatory and internal standards.
• Evaluate and close deviations, CAPAs, and change controls related to batch production.
• Make informed decisions on batch release, ensuring product quality and regulatory compliance.
• Compile, maintain and drive traceable and auditable batch release documentation.
• Collaborate with the relevant operational teams to support timely batch release.
• Prioritize QA activities to align with production schedules and delivery commitments.
• Identify and mitigate quality-related risks that could impact OTIF performance.
• Monitor and report on QA-related OTIF metrics and drive continuous improvement initiatives
• Train new staff members on SOPs in transition period (including GMP induction).
• Perform GMP training to support adherence to the GMP training schedule.
• Identify refresher or awareness training needs across the site.
• Prepare for and support internal audits, regulatory inspections (e.g., SAHPRA, FDA, etc.), and customer audits.
• Track and close audit findings and ensure timely implementation of corrective actions.
• Maintain audit readiness across all departments.
• Monitor manufacturing operations to ensure compliance with cGMP, GxP, and internal SOPs.
• Conduct routine inspections and compliance walkthroughs on the production floor.
• Provide real-time QA support during critical manufacturing and cleaning operations.
• Ensure plant floor activities align with quality and safety standards.
• Risk assessment participation, review and approval.
• Support IQ/OQ/PQ activities pertaining to validation.
• Review and approve cross contamination assessments.
• Perform, review and approve line clearance authorizations.
• Support the implementation and maintenance of the site’s Quality Management System (QMS).
• Participate in investigations of non-conformances and implement corrective and preventive actions.
• Independently assess deviations and non-conformances and make timely quality decisions.
• Ensure data integrity and compliance with ALCOA+ principles across all quality records.
• Assist in the development and revision of SOPs, work instructions, and training materials.
• Write, review and approve technical reports related to deviations, CAPAs, and change controls
  
  

Background/Experience

Skills Required

• Minimum a tertiary qualification - bachelor’s degree in pharmacy, Chemistry, Microbiology, Biochemistry, or Chemical Engineering (NQF Level 7 or 8).
• cGMP and QMS experience - knowledge of ICH and FDA guidelines for API manufacturers and their application, and/or relevant Quality system certification.
• Experience in batch record review, batch release, and quality documentation.
• Must be computer literate, MS Windows, i.e., Word, Excel, PowerPoint, Teams, Adobe, etc.
• Validation, Regulatory, Quality Assurance, Quality Control and Production experience will be advantageous.
  
  

Competencies/Personal Attributes

• Observation - ability to observe and evaluate processes and procedures.
• Excellent organizational and administrative skills.
• Excellent problem-solving skills.
• Attention to detail - proofreading and auditing.
• Ability to work independently.
• Ability to interpret regulations and take initiative.
• Confident to address adverse issues at all levels of the business.
• Good interpersonal skills.
• Application of critical thinking to quality decisions.
• Effective communication and technical writing skills.
  
  

Suitably qualified applicants are invited to submit their CV’s online on or before the specified date. Preference will be given to applicants from designated groups in accordance with laws governing employment equity, where such laws are applicable to the Aspen entity that will employ the successful candidate. If you have not heard from the HR department within 30 days of this advert closing, please consider your application unsuccessful.

#AM

Seniority level

• Seniority level Associate

Employment type

• Employment type Full-time

Job function

• Job function Health Care Provider
• Industries Pharmaceutical Manufacturing

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Join to apply for the QA Compliance Inspectors role at Aspen Pharma Group Join to apply for the QA Compliance Inspectors role at Aspen Pharma Group Fine Chemicals Corporation requires the services of QA Compliance Inspectors for our Quality Assurance Department.OverviewResponsible for ensuring that all manufacturing activities at the facility comply with current Good Manufacturing Practices (c GMP), regulatory requirements, and internal quality standards. To provide oversight of batch documentation, batch release, audit readiness, OTIF (On-Time In-Full) support, and plant floor compliance monitoring. Collaborate with production, QC, and engineering teams to ensure GMP compliance and product quality. Promote a culture of quality and compliance across operations. ResponsibilitiesReview and approve Batch Production Records (BPRs), cleaning logs, and associated documentation. Ensure completeness, accuracy, and compliance of batch records with regulatory and internal standards. Evaluate and close deviations, CAPAs, and change controls related to batch production. Make informed decisions on batch release, ensuring product quality and regulatory compliance. Compile, maintain and drive traceable and auditable batch release documentation. Collaborate with the relevant operational teams to support timely batch release. Prioritize QA activities to align with production schedules and delivery commitments. Identify and mitigate quality-related risks that could impact OTIF performance. Monitor and report on QA-related OTIF metrics and drive continuous improvement initiatives Train new staff members on SOPs in transition period (including GMP induction). Perform GMP training to support adherence to the GMP training schedule. Identify refresher or awareness training needs across the site. Prepare for and support internal audits, regulatory inspections (e.g., SAHPRA, FDA, etc.), and customer audits. Track and close audit findings and ensure timely implementation of corrective actions. Maintain audit readiness across all departments. Monitor manufacturing operations to ensure compliance with c GMP, Gx P, and internal SOPs. Conduct routine inspections and compliance walkthroughs on the production floor. Provide real-time QA support during critical manufacturing and cleaning operations. Ensure plant floor activities align with quality and safety standards. Risk assessment participation, review and approval. Support IQ/OQ/PQ activities pertaining to validation. Review and approve cross contamination assessments. Perform, review and approve line clearance authorizations. Support the implementation and maintenance of the site’s Quality Management System (QMS). Participate in investigations of non-conformances and implement corrective and preventive actions. Independently assess deviations and non-conformances and make timely quality decisions. Ensure data integrity and compliance with ALCOA+ principles across all quality records. Assist in the development and revision of SOPs, work instructions, and training materials. Write, review and approve technical reports related to deviations, CAPAs, and change controls Background/ExperienceSkills RequiredMinimum a tertiary qualification - bachelor’s degree in pharmacy, Chemistry, Microbiology, Biochemistry, or Chemical Engineering (NQF Level 7 or 8). c GMP and QMS experience - knowledge of ICH and FDA guidelines for API manufacturers and their application, and/or relevant Quality system certification. Experience in batch record review, batch release, and quality documentation. Must be computer literate, MS Windows, i.e., Word, Excel, Power Point, Teams, Adobe, etc. Validation, Regulatory, Quality Assurance, Quality Control and Production experience will be advantageous. Competencies/Personal AttributesObservation - ability to observe and evaluate processes and procedures. Excellent organizational and administrative skills. Excellent problem-solving skills. Attention to detail - proofreading and auditing. Ability to work independently. Ability to interpret regulations and take initiative. Confident to address adverse issues at all levels of the business. Good interpersonal skills. Application of critical thinking to quality decisions. Effective communication and technical writing skills. Suitably qualified applicants are invited to submit their CV’s online on or before the specified date. Preference will be given to applicants from designated groups in accordance with laws governing employment equity, where such laws are applicable to the Aspen entity that will employ the successful candidate. If you have not heard from the HR department within 30 days of this advert closing, please consider your application unsuccessful.#AM Seniority level Seniority level Associate Employment type Employment type Full-time Job function Job function Health Care Provider Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Aspen Pharma Group by 2x Sign in to set job alerts for “Quality Assurance Inspector” roles. We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr

Fine Chemicals Corporation requires the services of QA Compliance Inspectors for our Quality Assurance Department.

Overview

• Responsible for ensuring that all manufacturing activities at the facility comply with current Good Manufacturing Practices (cGMP), regulatory requirements, and internal quality standards.
• To provide oversight of batch documentation, batch release, audit readiness, OTIF (On-Time In-Full) support, and plant floor compliance monitoring.
• Collaborate with production, QC, and engineering teams to ensure GMP compliance and product quality.
• Promote a culture of quality and compliance across operations.

Responsibilities

• Review and approve Batch Production Records (BPRs), cleaning logs, and associated documentation.
• Ensure completeness, accuracy, and compliance of batch records with regulatory and internal standards.
• Evaluate and close deviations, CAPAs, and change controls related to batch production.
• Make informed decisions on batch release, ensuring product quality and regulatory compliance.
• Compile, maintain and drive traceable and auditable batch release documentation.
• Collaborate with the relevant operational teams to support timely batch release.
• Prioritize QA activities to align with production schedules and delivery commitments.
• Identify and mitigate quality-related risks that could impact OTIF performance.
• Monitor and report on QA-related OTIF metrics and drive continuous improvement initiatives
• Train new staff members on SOPs in transition period (including GMP induction).
• Perform GMP training to support adherence to the GMP training schedule.
• Identify refresher or awareness training needs across the site.
• Prepare for and support internal audits, regulatory inspections (e.g., SAHPRA, FDA, etc.), and customer audits.
• Track and close audit findings and ensure timely implementation of corrective actions.
• Maintain audit readiness across all departments.
• Monitor manufacturing operations to ensure compliance with cGMP, GxP, and internal SOPs.
• Conduct routine inspections and compliance walkthroughs on the production floor.
• Provide real-time QA support during critical manufacturing and cleaning operations.
• Ensure plant floor activities align with quality and safety standards.
• Risk assessment participation, review and approval.
• Support IQ/OQ/PQ activities pertaining to validation.
• Review and approve cross contamination assessments.
• Perform, review and approve line clearance authorizations.
• Support the implementation and maintenance of the site’s Quality Management System (QMS).
li>Participate in investigations of non-conformances and implement corrective and preventive actions.
• Independently assess deviations and non-conformances and make timely quality decisions.
• Ensure data integrity and compliance with ALCOA+ principles across all quality records.
• Assist in the development and revision of SOPs, work instructions, and training materials.
• Write, review and approve technical reports related to deviations, CAPAs, and change controls

Skills Required

Background/Experience

•  Minimum a tertiary qualification – bachelor’s degree in pharmacy, Chemistry, Microbiology, Biochemistry, or Chemical Engineering (NQF Level 7 or 8).
• < i>Experience in batch record review, batch release, and quality documentation.
• Must be computer literate, MS Windows, i.e., Word, Excel, PowerPoint, Teams, Adobe, etc.
• Validation, Regulatory, Quality Assurance, Quality Control and Production experience will be advantageous.

Competencies/Personal Attributes

• Observation – ability to observe and evaluate processes and procedures.
li>Excellent organizational and administrative skills.
• Excellent problem-solving skills.
• Attention to detail – proofreading and auditing.
li>Ability to work independently.
• Ability to interpret regulations and take initiative.
• Confident to address adverse issues at all levels of the business.
• Good interpersonal skills.
• Application of critical thinking to quality decisions.
• Effective communication and technical writing skills.

Suitably qualified applicants are invited to submit their CV’s online on or before the specified date. Preference will be given to applicants from designated groups in accordance with laws governing employment equity, where such laws are applicable to the Aspen entity that will employ the successful candidate. If you have not heard from the HR department within 30 days of this advert closing, please consider your application unsuccessful.

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Location: Johannesburg, Gauteng, South Africa, 2091

Howden, a Chart Industries Company, is a global engineering business that focuses on providing clients with industrial products that help multiple sectors improve their everyday processes. Howden’s core focus is on providing quality solutions for air and gas handling, and have over a century of experience in doing so.

What Will You Do?

• Conduct Quality audits according to schedule and compile audit reports accurately, on time, and in accordance with procedure. Raise, follow up and close audit findings.
• Ensure Calibration Status of Howden Power measuring and Test equipment is maintained.
• Supplier inspections: Undertake surveillances, audits, dimensional, visual and welding inspections and report on conformance to Project engineers. Authorise the release of items to site to indicate quality conformance
• Initiate, follow up and close out of Non-Conformance Reports (NCR) on products found to be non-compliant
• Prepare, review and monitor Quality Control plans to ensure that the quality system and contractual quality requirements are adhered to and ensure that Project Quality requirements are communicated to all relevant parties.
• Verify and ensure Suppliers are working in accordance with the Latest copies of Howden Power purchase Specifications and Procedures.
• Provide assistance to in-house inspections when required
• Expedite progress on additional Orders at suppliers during inspections.
• Conduct Quality training in-house and with supplier personnel in line with the agreed annual programme, thereby creating quality awareness, which will lead to continuous improvement and development.

Your Experience Should Be.

• Grade 12
• At least 5 years’ experience as an artisan Boilermaker/Fitter and Turner, having sufficient experience to manufacture structural steel and plate work to drawings.
• Ability to read and interpret technical drawings and specifications
• Knowledgeable on the use and applications of various measuring and test equipment.
• Welding and Fabrications Inspector Level 1 and 2, and an understanding of welding/ fabrication defects.
• Knowledge of various NDT methods and procedures.
• Computer literacy – Microsoft Office Suite, particularly Word.
• Good problem-solving skills.
• ISO 9000 Quality Management Systems training.
• Internal/ Supplier audit on quality management system courses.

Our Benefits Package.

Howden provides a great benefits package in addition to an attractive salary. The Company also offers the opportunity to work in an exciting, fast-paced environment within a global engineering company.

Chart Industries, Inc. is a leading independent global manufacturer of highly engineered equipment servicing multiple applications in the Energy and Industrial Gas markets. Our unique product portfolio is used in every phase of the liquid gas supply chain, including upfront engineering, service and repair.

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Quality Compliance Inspector
**Location:** Johannesburg, Gauteng, South Africa, 2091
**Company:** Chart Industries
**_Ensuring Chart's Success._**
Howden, a Chart Industries Company, is a global engineering business that focuses on providing clients with industrial products that help multiple sectors improve their everyday processes. Howden's core focus is on providing quality solutions for air and gas handling, and have over a century of experience in doing so.
We invite you to join Howden South Africa as a Quality Compliance Inspector. We are looking for an experienced Inspector to effectively monitor quality standard compliance for the Business Unit.
**_What Will You Do?_**
+ Conduct Quality audits according to schedule and compile audit reports accurately, on time, and in accordance with procedure. Raise, follow up and close audit findings.
+ Ensure Calibration Status of Howden Power measuring and Test equipment is maintained.
+ Supplier inspections: Undertake surveillances, audits, dimensional, visual and welding inspections and report on conformance to Project engineers. Authorise the release of items to site to indicate quality conformance
+ Initiate, follow up and close out of Non-Conformance Reports (NCR) on products found to be non-compliant
+ Prepare, review and monitor Quality Control plans to ensure that the quality system and contractual quality requirements are adhered to and ensure that Project Quality requirements are communicated to all relevant parties.
+ Verify and ensure Suppliers are working in accordance with the Latest copies of Howden Power purchase Specifications and Procedures.
+ Provide assistance to in-house inspections when required
+ Expedite progress on additional Orders at suppliers during inspections.
+ Conduct Quality training in-house and with supplier personnel in line with the agreed annual programme, thereby creating quality awareness, which will lead to continuous improvement and development.
**_Your Experience Should Be._**
+ Grade 12
+ At least 5 years' experience as an artisan Boilermaker/Fitter and Turner, having sufficient experience to manufacture structural steel and plate work to drawings.
+ Ability to read and interpret technical drawings and specifications
+ Knowledgeable on the use and applications of various measuring and test equipment.
+ Welding and Fabrications Inspector Level 1 and 2, and an understanding of welding/ fabrication defects.
+ Knowledge of various NDT methods and procedures.
+ Computer literacy - Microsoft Office Suite, particularly Word.
+ Good problem-solving skills.
+ ISO 9000 Quality Management Systems training.
+ Internal/ Supplier audit on quality management system courses.
**_Our Benefits Package._**
Howden provides a great benefits package in addition to an attractive salary. The Company also offers the opportunity to work in an exciting, fast-paced environment within a global engineering company.
Chart Industries is an equal employment opportunity (EEO) employer and will not discriminate against any employee or applicants because of his or her race, color, religion, sex, gender identity or expression, sexual orientation, pregnancy, age, national origin, disability, veteran status, military status, marital status, genetic information or any other reason prohibited by law. Additionally, it is and shall continue to be our policy to provide promotion and advancement opportunities in a non-discriminatory fashion.
Chart complies with applicable local, state, and federal statutes governing "equal employment opportunity" and nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including hiring, placement, promotion, termination, layoff, recall, transfers, leave of absence, compensation and training.

Kurzer Überblick

Kiwa BCS Öko-Garantie GmbH from Nuremberg is part of the Kiwa Group, one of the world's 20 leading companies in the TIC industry (testing, inspection, certification) and is already active in over 90 countries. Kiwa BCS is one of the pioneers of the organic movement in Europe and the first state-approved organic inspection body in Germany (1992). As an approved and private inspection body, we carry out inspections and certifications in all areas of organic agriculture for farmers, industry, contract processors, importers/exporters and logistics companies at home and abroad. In addition to EU organic certification, we offer further national and international certifications according to various recognised organic, Fairtrade and sustainability standards on four continents. For example: NOP, JAS, KOC, OSKSA, GOTS, ASC/MSC, Rainforest Alliance and many more. Controls on behalf of associations such as Demeter, Biokreis, Naturland (Fair), BioSuisse and Bioland are also part of our services.

Dafür suchen wir Sie

• Carrying out organic inspections according to the EU Organic Regulation, USDA NOP and JAS
• Carrying out inspections according to the standards of various organic farming associations (e.g., Naturland)
• Compilation of inspection reports and associated evidence
• Inspection assignments in the region agreed with you, as well as scheduling of the inspection assignments on your own responsibility and thus full control over the organisation of the inspection tour
  
  

Das bringen Sie mit?

• Residence in South Africa
• Completed studies in agriculture or food technology
• Knowledge education/experiences in organic farming is a must
• Minimum of 2 years’ experience in organic auditing (agriculture and food processing/ trade)
• Knowledge of USDA NOP and related international organic standards
• Detail-oriented, with excellent oral and written communication skills
• Able to clearly communicate complex technical information in a positive and effective way
• English (fluent) - other languages are a great advantage
• Willingness to travel within the region of local and international
• Advanced skills with well-known software programs, e.g., Microsoft to deliver digital inspection documents
  
  

Das können Sie von uns erwarten?

• Comprehensive introduction to our systems and processes
• Professional training on a regular base and further education opportunities
• Fair and reliable payment
• Permanent contact persons in our head office in Nuremberg / Germany
• The possibility of a long-term partnership

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Location: Loper Ave, Isando

Overview

The Quality Control Supervisor is responsible for ensuring that all manufactured products conform to the company's quality, safety, and reliability standards. This includes implementing quality control systems, conducting inspections, leading the QC team, and driving continuous improvement.

Responsibilities Quality Control Planning & Inspection

• Develop and implement quality control procedures and protocols in line with company and regulatory requirements.
• Conduct regular audits and inspections of processes, products, and raw materials.
• Perform product testing, data capture, analysis, and statistical control.
• Document non-conformances and ensure corrective actions are implemented.
• Qualify measuring equipment and ensure correct application of tolerance, sampling, and measurement techniques.

Team Leadership & Personnel Management

• Lead, train, motivate, and manage QC Inspectors, Assistants, and Facilitators.
• Oversee attendance, timesheets, disciplinary compliance, and shift rosters.
• Monitor production output, downtime, deviations, and ensure accurate recording.
• Conduct regular performance reviews and provide coaching, counselling, and recognition.
• Mentor team members in industrialized measuring techniques and sustainable processes.

Customer Service

• Respond to customer inquiries related to product quality.
• Investigate and resolve quality-related complaints in collaboration with sales and production teams.

Reporting & Administration

• Ensure daily shift handovers are conducted effectively.
• Oversee reporting on audits, inspections, deviations, and corrective actions.

Health, Safety & Food Safety

• Ensure compliance with health, safety, and housekeeping standards in all QC areas.
• Report hazards, incidents, and near misses promptly.
• Enforce adherence to Good Manufacturing Practices (GMP) and Food Safety Management Systems (FSMS).

Continuous Improvement & Self-Development

• Stay updated with regulatory changes, industry standards, and technological advancements.
• Drive improvements in QC processes, systems, and team performance.
• Serve as a role model by promoting company values, professionalism, and best practices.

Qualifications & Experience

• Education: Matric (Grade 12).
• Tertiary: NQF 4 Supervisory Management Qualification & Certificate in Quality Control.
• Experience: Minimum 8 years experience in the manufacturing industry, with proven leadership in quality control.

Competencies

• Strong technical knowledge of manufacturing processes, equipment, and raw materials.
• Solid understanding of quality systems and certifications.
• Excellent people management, conflict management, and diversity management skills.
• Strong administrative and reporting capabilities.
• Analytical and problem-solving mindset with exceptional attention to detail.
• Ability to make sound business-aligned decisions in operational environments.

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To ensure that all materials and processes adhere strictly to customer specifications and internal quality standards, and to oversee the implementation and compliance of quality systems within the production division.

• PRINCIPAL ACCOUNTABILITIES

Accountabilities

Key Performance Indicators (KPIs)

Support in determining, negotiating, and agreeing upon in-house quality procedures, standards, and specifications

Clearly documented quality procedures aligned with ISO and customer expectations

Ensure adherence to quality, health, and safety standards across the plant

Zero non-conformities and audit failures; reduced incident reports

Monitor and ensure that manufacturing processes comply with defined quality standards

Regular inspections, compliance audits, and corrective actions documented and implemented

Conduct and document quality testing (pre-production, in-process, and final product)

100% completion of quality checklists and sampling reports

Follow established procedures, ISO guidelines, and maintain proper documentation

ISO compliance and audit-readiness at all times

Act as a catalyst for continuous improvement in quality and operational efficiency

Number of improvement initiatives implemented per quarter; measurable performance improvements

Lead, manage and motivate quality control staff to meet departmental goals

Achievement of departmental KPIs; performance reviews and development plans completed on time

Monitor and document critical control points (CCPs) regularly

Accurate and timely CCP logs with corrective actions recorded

Ensure customer requirements and service standards are understood and implemented

Positive customer feedback; low rate of quality-related returns or complaints

• INTERACTIONS

Internal :

• Production Department
• Purchase / Procurement
• Planning and Production Control (PPC)
• Maintenance and R&D (as applicable)

External :

• Customers and end-users (for quality audits, complaints, and resolution)
• Raw material vendors and external testing laboratories
• Certification bodies (for ISO or regulatory audits)
• SKILLS AND KNOWLEDGE

Educational Qualifications :

• Post Graduate Diploma in Plastics Technology / CIPET or
• Diploma in Plastics / Mechanical Engineering or related field

Relevant Industry Experience :

• 5–7 years of experience in a Packaging Manufacturing Industry with hands-on exposure to Quality Control and Assurance

Technical Skills :

• In-depth knowledge of packaging processes (lamination, extrusion, printing, slitting, sealing)
• Experience with lab instruments and testing procedures (tensile strength, bond strength, GSM, COF, WVTR, etc.)
• Proficiency in ISO 9001 / ISO 22000 / HACCP and other quality management systems
• Skilled in preparing audit documentation, process documentation, and quality SOPs

Behavioral Skills :

• Strong analytical and problem-solving ability
• Detail-oriented with a commitment to accuracy and process compliance
• Effective communicator and team leader
• Ability to manage cross-functional teams under pressure

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Quality Control Assistant • Centurion, South Africa

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JOB PURPOSE

To ensure that all materials and processes adhere strictly to customer specifications and internal quality standards, and to oversee the implementation and compliance of quality systems within the production division.

• PRINCIPAL ACCOUNTABILITIES

Accountabilities

Key Performance Indicators (KPIs)

Support in determining, negotiating, and agreeing upon in-house quality procedures, standards, and specifications

Clearly documented quality procedures aligned with ISO and customer expectations

Ensure adherence to quality, health, and safety standards across the plant

Zero non-conformities and audit failures; reduced incident reports

Monitor and ensure that manufacturing processes comply with defined quality standards

Regular inspections, compliance audits, and corrective actions documented and implemented

Conduct and document quality testing (pre-production, in-process, and final product)

100% completion of quality checklists and sampling reports

Follow established procedures, ISO guidelines, and maintain proper documentation

ISO compliance and audit-readiness at all times

Act as a catalyst for continuous improvement in quality and operational efficiency

Number of improvement initiatives implemented per quarter; measurable performance improvements

Lead, manage and motivate quality control staff to meet departmental goals

Achievement of departmental KPIs; performance reviews and development plans completed on time

Monitor and document critical control points (CCPs) regularly

Accurate and timely CCP logs with corrective actions recorded

Ensure customer requirements and service standards are understood and implemented

Positive customer feedback; low rate of quality-related returns or complaints

• INTERACTIONS

Internal :

• Production Department
• Purchase / Procurement
• Planning and Production Control (PPC)
• Maintenance and R&D (as applicable)

External :

• Customers and end-users (for quality audits, complaints, and resolution)
• Raw material vendors and external testing laboratories
• Certification bodies (for ISO or regulatory audits)
• SKILLS AND KNOWLEDGE

Educational Qualifications :

• Post Graduate Diploma in Plastics Technology / CIPET or
• Diploma in Plastics / Mechanical Engineering or related field

Relevant Industry Experience :

• 5–7 years of experience in a Packaging Manufacturing Industry with hands-on exposure to Quality Control and Assurance

Technical Skills :

• In-depth knowledge of packaging processes (lamination, extrusion, printing, slitting, sealing)
• Experience with lab instruments and testing procedures (tensile strength, bond strength, GSM, COF, WVTR, etc.)
• Proficiency in ISO 9001 / ISO 22000 / HACCP and other quality management systems
• Skilled in preparing audit documentation, process documentation, and quality SOPs

Behavioral Skills :

• Strong analytical and problem-solving ability
• Detail-oriented with a commitment to accuracy and process compliance
• Effective communicator and team leader
• Ability to manage cross-functional teams under pressure

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