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assistant manager quality assurance Jobs in Karachi

assistant manager quality assurance

assistant manager supplier quality assurance Jobs in Karachi

assistant manager supplier quality assurance

quality control specialist

Novaplast Custom Molders

Novaplast Custom Molders is a leading manufacturer of precision plastic components for the automotive industry. We are seeking a skilled Quality Control Inspector with experience in the automotive manufacturing industry. The candidate will be responsible for ensuring product quality, monitoring in-process production, and maintaining compliance with defined quality standards.Responsibilities:<ul><li>Perform in-process, final inspection, and incoming material inspection as per quality standards.</li><li>Check parts visually and dimensionally using gauges, vernier calipers, micrometers, and other measuring instruments.</li><li>Monitor production lines to ensure adherence to work instructions and control plans.</li><li>Identify defects, record non-conformities, and coordinate with production for corrective actions.</li><li>Prepare inspection reports and maintain QC documentation.</li><li>Ensure implementation of 5S and safety standards within the inspection area.</li><li>Support QA/QC team in root cause analysis and continual improvement activities.</li></ul>Skills Required:<ul><li>Knowledge of inspection tools (calipers, micrometers, gauges).</li><li>Strong understanding of automotive quality standards and processes.</li><li>Proficiency in using CAD/CREO software is a plus point.</li><li>Basic knowledge of molding processes will be an advantage.</li><li>Good communication and documentation skills.</li><li>Ability to work in a team and handle multiple quality-related tasks.</li></ul>Qualification:<ul><li>Diploma in Mechanical (Pak-Swiss Training Centre &ndash; preferred/required).</li></ul>Experience:<ul><li>Minimum 2 years of QA/QC experience in an auto parts manufacturing company.</li></ul>Gender: MaleRequirement: Immediate JoiningTimings: 8:30 AM-6:00 PM (Mon-Sat)Location: North Nazimabad, Block B, KarachiEmail: Also send your resume on jobs@novaplast.pkJob Type: Full-timePay: Rs35,000.00 - Rs40,000.00 per monthWork Location: In person

Quality Inspector

OPTIMIZE ENGINEERING CORE PVT. LTD

Job Location: Port Qasim Karachi PakistanIndustry: Engineering - Production PlantWorking machinery in the quality department: Tensile Testing machine, damp heat test chamber humility, thermal shock tester, pressure testerProduct Nature: Mechanical (Mainly Evaporator Production&amp; appliances partsResponsibilities<ul><li>Incoming raw material, Inprocess and final product inspection and quality control</li><li>Monitoring customer feedback and maintaining documents of QDR, RCCA, FMEA, calculating process capability etc</li><li>Analyzing inprocess rejection with possible root cause , suggest and implement countermeasures.</li><li>Coordinate with production team in implementing standard working procedure for operators and quality control inspectors</li></ul>Performance Indicator<ul><li>Updated ISO documentation.</li><li>Minimize repetitive Failure</li><li>Timely completion of all activities</li><li>Management of the review meetings, Obeya Reports.</li><li>Regular inter department communication.</li><li>Spending as per approved budget</li><li>Kaizen KPI</li></ul>Requirements:<ul><li>02 to 03 Years of Quality control experience in an engineering-based appliance production firm</li><li>B.E/M.E Mechanical from a reputed institute</li><li>Certification in quality will be plus point</li><li>Working knowledge of Quality standards &amp; tools</li><li>Familiarity in drafting Quality reports</li><li>Effective communication and people management skills</li><li>Experience in handling quality inspection team</li></ul>Job Type: Full-timeApplication Question(s):<ul><li>What's your current salary?</li><li>Current benefits?</li><li>Expected joining date?</li><li>Expected Salary?</li><li>Where do you live in karachi? mention exact area.</li><li>Why you want to leave your current job?</li></ul>Education:<ul><li>Bachelor's (Required)</li></ul>Experience:<ul><li>Quality Control: 3 years (Preferred)</li></ul>Language:<ul><li>English &amp; Urdu (Preferred)</li></ul>Work Location: In person

Quality Control Engineer

Minerva Research Solutions

<div>JOB DESCRIPTION: 
 
Minerva Research Solutions is a clinical trial management service provider. We aim to transform the landscape of healthcare and research with our quality clinical services. We support the biotech, medical, and pharma industries through all phases of the clinical trial lifecycle.
Our services include Data Operation, Recruitment Services, and Regulatory. Our goal is to speed up the lifecycle of novel therapies through streamlined processes, stringent timelines &amp; real-time solutions. Our clinical trial support services &amp; consultations are tailored to foster your product and requirements. 
 
We aim to deliver high-quality data and solutions to make your clinical trials a success. We follow stringent FDA and GCP regulations throughout all phases of the clinical trial process. 
 
Minerva Research Solution is looking for dynamic individuals with a passion for ensuring the highest standards in clinical trial data quality assurance. As a key player in our team, you will play a crucial role in maintaining the integrity and accuracy of clinical trial data.
Responsibilities:<ul><li>
Perform comprehensive data-driven Quality Monitoring activities to ensure compliance with regulatory requirements and SOPs, and to ensure a continued state of inspection readiness.</li><li>
Ensure data is recorded under sponsor protocol, GCP guidelines, industry guidelines, and agency regulations.</li><li>
Perform quality control checks; identify and track source documentation errors and non-conformances with requirements.</li><li>
Provide ongoing compliance support including but not limited to:</li><li>
Preparing periodic clinical trial quality reports for assigned programs and assessing these reports with applicable clinical team members to identify areas of risk. Collaborates with applicable team members to develop risk mitigation plans.</li><li>
Collaborating with the Clinical Team to share audit/inspection observations for lessons learned across protocol, and/or program, and working with appropriate groups to implement Corrective Action Plans (CAPAs).</li><li>
Performs quality reviews of key documents developed for use in clinical trials and in preparation for submission to regulatory health authorities.</li><li>
Assist in preparing for all Sponsor and FDA audits.</li><li>
Assist in conducting internal audits to review key processes.</li><li>
Provide appropriate support to assigned cross-functional workgroups.</li><li>
Establishes effective partnerships with internal staff to facilitate the timely identification and resolution of compliance and quality matters and other opportunities for quality process improvement.</li><li>
Query resolution and data entry and questionnaire preparation regarding the respective studies.</li><li>
Other related Quality Assurance projects as assigned.</li><li>
The QA Associate will report to the Quality Assurance Lead</li></ul>
Knowledge, Education, and Experience:<ul><li>
Qualified Profession with strong medical background (Pharm-D, MBBS, BDS etc) with a keen interest in Clinical Research are strongly encouraged to apply.</li><li>
In-depth knowledge of FDA, GCP, ICH, and other state and federal agency guidelines for the conduct of clinical trials.</li><li>
Knowledge of IRB requirements.</li><li>
1+ years in work related to Quality Control / Quality Assurance area in clinical research will preferred..</li><li>
Experience including external clinical/regulatory and document auditing will be a plus</li></ul>
Skills and Abilities:<ul><li>
Good communication skills (interpersonal, written, verbal)</li><li>
Strong attention to detail and good time management skills</li><li>
Flexible attitude concerning work assignments</li><li>
Ability to manage multiple and varied tasks in a fast-moving environment</li><li>
Ability to interact professionally at all levels within the organization.</li><li>
Knowledge of the HIPAA Privacy Act and its application to clinical research.</li></ul>
Benefits:<ul><li>
Competitive salary and performance-based bonuses.</li><li>
Medical health insurance coverage.</li><li>
Employees Old-age benefits coverage.</li><li>
Flexible work hours and remote work options.</li><li>
Professional learning and development support.</li><li>
Generous vacation and paid time off.</li><li>
Employee assistance programs for mental health.</li><li>
Company-sponsored events and team-building activities.</li><li>
Diverse, professional, and inclusive work environment.</li><li>
Opportunities for career growth.</li><li>
Cutting-edge technology and tools.</li><li>
Family-friendly policies, including parental leave.</li><li>
Commuter benefits or transportation assistance.</li><li>
Social responsibility and community involvement programs.</li></ul>
Openings:
04 positions 
Full-time 
On-site job 
 
Work Schedule Timings: 
Monday to Friday 
Evening Shift (07 PM to 03 AM) 
(transport facility provided for female staff only and allowance for male employees, additional night shift allowance)
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Clinical Trials Quality Assurance Associate (Night)

Reckitt

<div>
 We are Reckitt
 
 
 Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege.
 
 
 Research &amp; Development
 
 
 In Research and Development, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance.
 
 
 We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.
 
 
 The size of our organisation means you'll have the opportunity to learn and work in different functions within R&amp;D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation.
 
 
 
 About The Role
 
 
 
 We're in search of a proactive Quality Associate to join the Reckitt team, where innovation and science converge to make a real-world impact. You'll contribute to the growth of our trusted product portfolio, ensuring the highest standards of quality. Your expertise will drive activities from concept to execution, fostering an environment of continuous improvement. If you thrive in a dynamic atmosphere and are looking for a role where your actions directly contribute to the company's success, we would love to see your application.
 
 
 The scope of the job includes assistance to Quality Compliance Manager in overseeing Quality Compliance at the Reckitt Factory, including both Healthcare and Household plants.
 
 
 Your responsibilities
 
 
 <ul>
 <li>
 Analyzing and updating existing compliance policies and related documentation.
 </li>
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 Training employees in industry compliance requirements.
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 Ensure that Quality Improvement/remediation plans are followed and report to Quality Compliance Manager of any deviation or non-conformance.
 </li>
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 Evaluating internal operational and procedural compliance.
 </li>
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 Communicating compliance policies and guidelines to Management and designated departments.
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 Executing new compliance policies and procedures as required.
 </li>
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 Applying for compliance certification and regulatory approval.
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 Developing and maintaining a compliance record keeping system.
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 Corresponding with the Ministry of Health Officials pertaining to registered products.
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 Conduct Self-Inspection Audits along with CAPA Finalization with auditee and track their on-time execution.
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 Perform risk assessment on an annual basis based on criticality of operations for Quality Internal audit scheduling and prioritization and develop Master plan in accordance with risk-based approach.
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 Proactively audit processes, practices and ensure actions to identify weaknesses.
 </li>
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 Track internal inspection commitments through action, completion and verification.
 </li>
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 Conduct training sessions for Management &amp; Non-Management staff.
 
 
 </li>
 </ul>
 The experience we're looking for
 
 
 <ul>
 <li>
 Educate to a minimum bachelor&rsquo;s degree level in Pharmacy / Chemistry from a recognized university.
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 Minimum 2 years hands-on experience in Quality Assurance / Compliance in Pharmaceutical industry / FMCG company.
 </li>
 <li>
 Knowledge of applicable regulatory requirements for GXP compliance.
 </li>
 <li>
 Knowledge of all aspects relating to QC &amp; QA of Pharmaceutical &amp; FMCG Products.
 </li>
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 Good communication and inter / intrapersonal skills. Must have ability to influence at all levels within the organization.
 </li>
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 Proficiency in using Microsoft Office and statistical analysis software.
 
 
 </li>
 </ul>
 The skills for success
 
 
 Commercial Awareness, Business Partnership, Collaboration, Partnership building, Ability to challenge the status quo, Propose improvement, Accountability, Adaptability, Collaborator, R&amp;D, Product Lifecycle Management.
 
 
 What we offer
 
 
 With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy.
 
 
 Equality
 
 
 We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.
</div>

AM Compliance

AGILE HR

The QC Officer will conduct routine quality checks on raw materials, in-process items, and finished products while performing basic lab testing using instruments such as viscometers, spectrophotometers, and BCT.The role requires monitoring production processes for compliance with Food Safety, HACCP, and GLP standards, documenting results accurately, reporting deviations promptly, supporting corrective actions, maintaining proper sampling and lab hygiene, and assisting with audits, calibrations, and continuous improvement activities.Job Requirements The ideal candidate holds a BS in Food Science and Technology, Applied Chemistry, or Food Engineering and has at least one year of QC or lab experience in the food manufacturing sector.They should have working knowledge of Food Safety and HACCP practices, experience with common lab instruments, strong analytical and documentation skills, the ability to coordinate with production teams, and availability to work on-site in Korangi from 8 AM to 5 PM, Monday to Saturday.Job Type: Full-timePay: Rs55,000.00 - Rs70,000.00 per monthWork Location: In person

Quality Control Officer

Smart Wave Industries

one industrial unit require of qualifications and experience of an Mechanical and Electronic Engineer with expertise in HVAC control systems and electronic circuit board programming and repair.Experience and Education.Electronic Engineer in HVAC &amp; Control Systems Specialist.PEC Registered | PCB Programming | VRF Systems | PLC &amp; HMI Programming | Electrical Control SystemsEducation &amp; Certification:Bachelors in Electronic Engineering (PEC Registered)Eligibility in knowledge of all types Electronic circuits testing, reading, repairing, Specialized training in inverter &amp; non-inverter control system PCB cards.PLC Controllers &amp; HMI Programming: Development, testing, and installation for industrial automation.Certified in PLC Programming &amp; HMI DevelopmentMechanical Engineer :-Eligibility in Computer skills.<ul><li>AutoCAD (Must)</li><li>Carrier HAP or RHVAC (Basic)</li><li>Excel</li><li>Duct/piping layout basics</li><li>Interest in HVAC design field</li><li>Basic understanding of heat transfer &amp; thermodynamics</li><li>Good communication &amp; learning ability</li><li>Sensible &amp; latent heat</li><li>Psychrometric chart reading</li><li>DB/WB/RH, dew point</li><li>Refrigeration cycle (compressor, condenser, evaporator.</li></ul>Korangi industrial area near residential is helpful.Job Type: Full-timePay: Rs50,000.00 - Rs55,000.00 per monthWork Location: In personExpected Start Date: 10/12/2025

Mechanical and Electronic Engineer

Digitalise-Canada

Job Title : Operations Manager (Skincare Brand)Location : Karachi &ndash; Site AreaSalary : PKR 40,000-50,000 per monthRequirement : Must have own conveyance for field visitsWe are hiring a smart, organized, and tech-savvy Operations Specialist to support day-to-day operations for our skincare brand. The right candidate should excel in vendor coordination, product material sourcing, and managing smooth production processes.Key Responsibilities:* Coordinate with vendors for sourcing skincare packaging, labels, raw materials, and printing items.* Manage production workflows, from printing to packaging and dispatch.* Conduct negotiations with suppliers to ensure competitive pricing and quality control.* Handle client and internal team communication efficiently and professionally.* Oversee product deliveries, follow-ups, and inventory updates.* Perform necessary field visits for vendor meetings, quality checks, and operational support.Requirements:* Must have strong communication and interpersonal skills.* Tech-savvy, quick learner, and able to manage multiple tasks smoothly.* Must have own transportation for site visits and vendor coordination.* Prior experience in skincare, cosmetics, or FMCG operations is a plus.Job Type: Full-timePay: Rs40,000.00 - Rs50,000.00 per monthApplication Question(s):<ul><li>Do you have your own conveyance for field visits within Karachi?</li><li>How many years of experience do you have in operations, supply chain, or vendor coordination?</li><li>Have you previously worked in a skincare, cosmetics, or FMCG-related role?</li><li>Are you comfortable handling vendor negotiations, material sourcing, and production follow-ups?</li><li>Are you willing to travel within the Site Area and other Karachi locations for operational tasks?</li><li>What is your highest level of education?</li><li>What is your last drawn Salary?</li><li>What is your expected monthly salary for this role?</li></ul>Work Location: In person

Operations Manager – Skin Care Brand

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