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manufacturing engineer

Dollar Industries Pvt. Ltd

Production Engineer &ndash; Assembly.We are seeking a Production Engineer (Assembly) with 2&ndash;3 years of experience in managing assembly line operations within a stationery, plastic processing, or consumer goods manufacturing environment.Key Responsibilities:<ul><li>Ensure achievement of production targets in quality, quantity, and timelines.</li></ul><ul><li>Monitor assembly machines, coordinate maintenance, and support new product trials.</li></ul><ul><li>Supervise daily production schedules and operator performance.</li></ul><ul><li>Implement process improvements, reduce waste, and uphold 6S and safety standards.</li></ul><ul><li>Coordinate with Plant Engineering, Quality, and Material teams for smooth operations.</li></ul>Requirements:<ul><li>B.E. in Mechanical or Industrial &amp; Manufacturing Engineering.</li></ul><ul><li>2&ndash;3 years of experience in automotive, industrial, or stationery assembly.</li></ul><ul><li>Proficient in CAD (AutoCAD preferred) with strong analytical and problem-solving skills.</li></ul><ul><li>Knowledge of production scheduling, process control, and Kaizen / 6S / QCC practices.</li></ul>Location: KarachiEmployment Type: Full-timeInterested candidates may send their CV by November 10, 2025, mentioning the position applied for in the subject line to: jobs@dollar-stationery.comJob Type: Full-timeWork Location: In person

Production Engineer – Assembly.

Amreli Steels Limited

<div>
 
 
 Join the #Amreli #Steels' Family!
 
 
 
 
 
 
 
 Amreli Steels Limited
 
 is seeking the talented individual for the position of
 
 Assistant Engineer Production in Rolling Plant
 
 to join our team. The ideal candidate will be primarily responsible for executing daily production activities, ensuring product quality, supervising and delegating tasks to the workforce, troubleshooting production-related issues, maintaining operational records&mdash;all while strictly adhering to established safety protocols and procedures.
 
 
 
 EDUCATION:
 
 
 
 BE - Mechanical or I&amp;M
 
 
 
 EXPERIENCE:
 
 
 
 3 - 5 years of relevant experience in manufacturing industry
 
 
 
 SKILLS:
 
 
 
 The ideal candidate should have production knowledge, strong troubleshooting skills, communicate effectively, and work under pressure in rotating shifts.
 
 
 
 LOCATION:
 
 
 
 Dhabeji SMS - Plant - Karachi.
 
</div>

Assistant Engineer

Habib Knit Fabrics (Pvt) Ltd.

Job Post :Chemical Enginieer Location : Korangi Industrial Area Korangi No 5 KarachiJob Summary:The Chemical Engineer will be responsible for monitoring chemical processes, ensuring product quality, maintaining safety standards, and supporting continuous improvement in the production area.Key Responsibilities:* Monitor and control chemical processes during production. * Ensure product quality meets required standards. * Conduct routine testing, sampling, and documentation. * Support process improvement and cost-saving initiatives. * Maintain safety compliance and follow all SOPs. * Troubleshoot process issues and assist in corrective actions. * Work with production and quality teams to maintain smooth operations. * Prepare daily reports and maintain records.Requirements:* Bachelor&rsquo;s degree in Chemical Engineering. * Basic knowledge of chemical processes, safety, and equipment. * Good analytical and problem-solving skills. * Ability to work in shifts if required. * Strong communication and teamwork skills. * Experience in manufacturing, textile, dyeing, or related industry. * Knowledge of ISO standards and safety protocols.Job Type: Full-timePay: Rs50,000.00 - Rs80,000.00 per monthEducation:<ul><li>Bachelor's (Preferred)</li></ul>Experience:<ul><li>Industrial: 3 years (Required)</li></ul>Work Location: In person

Chemical Enginieer

<div>Site Name: Pakistan - Sindh - Karachi 
Posted Date: Nov 17 2025 
We manufacture and supply reliable, high-quality medicines and vaccines to meet patients&rsquo; needs and drive our performance. 
Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it&rsquo;s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. 
We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients. 
 
You will validate and qualify equipment, systems, and utilities at our Pakistan site. You will work with engineering, quality, operations and external vendors to plan, execute, and document validation activities. We value people who are careful, curious, and collaborative. You will grow your technical skills, influence site reliability and compliance, and support GSK&rsquo;s mission of uniting science, technology and talent to get ahead of disease together. 
 
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:<ul><li>
Plan and execute validation lifecycle activities including design reviews, installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ).</li><li>
Ensure Computerized System Validation (CSV) at the site&mdash;including platforms like Kneat and CSQMS&mdash;by performing and documenting periodic compliance and validation reviews for all GxP and Non-GxP equipment, utilities, and facilities, in line with regulatory and corporate requirements.</li><li>
Prepare, review and maintain validation documents such as user requirements, validation plans, protocols, reports and traceability matrices.</li><li>
Support computerized system validation (CSV) and maintain compliance with site quality systems and validation policies.</li><li>
Coordinate commissioning and SAT activities with engineering, operations and external vendors.</li><li>
Lead new validation projects (e.g., URS, SIA, RTM, DQ/DR, CVP/IOQ protocols &amp; reports), maintain and update the validation tracker, and ensure all validation documentation is complete, timely, and accessible as per company policies.</li><li>
Actively participate in the Validation Working Party (VWP) to follow up on validation targets, resolve issues, and keep the Site Engineering Lead informed, ensuring all validation activities are aligned with defined timelines and standards.</li><li>
Collaborate with engineering, operations, and external vendors for commissioning and SAT activities. Offer technical support for utilities and automation systems (e.g., purified water, compressed air, HVAC, PLC-driven equipment), and engage in risk assessments and root cause analyses.</li></ul> 
Why You? 
 
Basic Qualification 
We are seeking professionals with the following required skills and qualifications to help us achieve our goals<ul><li>
Bachelor&rsquo;s degree in Engineering (Mechanical, Electrical, Chemical, Industrial) or Science</li><li>
Minimum 3 years&rsquo; experience in validation, engineering, or technical roles in a regulated manufacturing environment.</li><li>
Experience with IQ/OQ/PQ activities and preparing validation protocols and reports.</li><li>
Working knowledge of computerized system validation concepts and familiarity with validation documentation practices.</li><li>
Proficiency in MS Office for report writing and data presentation.</li><li>
Strong written and verbal communication skills and the ability to work with cross-functional teams.</li></ul> 
Preferred Qualification 
If you have the following characteristics, it would be a plus<ul><li>
Degree or certification in quality, validation, automation, or related field.</li><li>
Experience with PLCs, SCADA systems, and industrial automation.</li><li>
Experience using validation or quality management software.</li><li>
Knowledge of Pharmaceutical &amp; Sterile Manufacturing Systems and Clean Utilities Systems (Purified Water, HVAC, Steam) and their qualification.</li><li>
Experience in project work, commissioning of equipment, or managing vendors.</li><li>
Familiarity with regulatory expectations and good documentation practices in manufacturing environments.</li></ul> 
Work location and model 
This role is on-site at our Pakistan facility. Regular on-site presence is required to lead validation and commissioning activities. 
 
What we value 
We look for people who take responsibility, work openly with others, and focus on practical improvements. You will join a team that supports learning, growth and inclusion. We encourage clear, respectful communication and collaboration across teams. 
 
Ready to apply? 
If you are motivated to build your validation expertise and make an impact, we would like to hear from you. Please submit your CV and a short note explaining why this role interests you. We welcome candidates from varied backgrounds and encourage applications from all qualified people.
We manufacture and supply reliable, high-quality medicines and vaccines to meet patients&rsquo; needs and drive our performance. 
Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it&rsquo;s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. 
We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients. 
 
You will validate and qualify equipment, systems, and utilities at our Pakistan site. You will work with engineering, quality, operations and external vendors to plan, execute, and document validation activities. We value people who are careful, curious, and collaborative. You will grow your technical skills, influence site reliability and compliance, and support GSK&rsquo;s mission of uniting science, technology and talent to get ahead of disease together. 
 
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:<ul><li>
Plan and execute validation lifecycle activities including design reviews, installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ).</li><li>
Ensure Computerized System Validation (CSV) at the site&mdash;including platforms like Kneat and CSQMS&mdash;by performing and documenting periodic compliance and validation reviews for all GxP and Non-GxP equipment, utilities, and facilities, in line with regulatory and corporate requirements.</li><li>
Prepare, review and maintain validation documents such as user requirements, validation plans, protocols, reports and traceability matrices.</li><li>
Support computerized system validation (CSV) and maintain compliance with site quality systems and validation policies.</li><li>
Coordinate commissioning and SAT activities with engineering, operations and external vendors.</li><li>
Lead new validation projects (e.g., URS, SIA, RTM, DQ/DR, CVP/IOQ protocols &amp; reports), maintain and update the validation tracker, and ensure all validation documentation is complete, timely, and accessible as per company policies.</li><li>
Actively participate in the Validation Working Party (VWP) to follow up on validation targets, resolve issues, and keep the Site Engineering Lead informed, ensuring all validation activities are aligned with defined timelines and standards.</li><li>
Collaborate with engineering, operations, and external vendors for commissioning and SAT activities. Offer technical support for utilities and automation systems (e.g., purified water, compressed air, HVAC, PLC-driven equipment), and engage in risk assessments and root cause analyses.</li></ul> 
Why You? 
 
Basic Qualification 
We are seeking professionals with the following required skills and qualifications to help us achieve our goals<ul><li>
Bachelor&rsquo;s degree in Engineering (Mechanical, Electrical, Chemical, Industrial) or Science</li><li>
Minimum 3 years&rsquo; experience in validation, engineering, or technical roles in a regulated manufacturing environment.</li><li>
Experience with IQ/OQ/PQ activities and preparing validation protocols and reports.</li><li>
Working knowledge of computerized system validation concepts and familiarity with validation documentation practices.</li><li>
Proficiency in MS Office for report writing and data presentation.</li><li>
Strong written and verbal communication skills and the ability to work with cross-functional teams.</li></ul> 
Preferred Qualification 
If you have the following characteristics, it would be a plus<ul><li>
Degree or certification in quality, validation, automation, or related field.</li><li>
Experience with PLCs, SCADA systems, and industrial automation.</li><li>
Experience using validation or quality management software.</li><li>
Knowledge of Pharmaceutical &amp; Sterile Manufacturing Systems and Clean Utilities Systems (Purified Water, HVAC, Steam) and their qualification.</li><li>
Experience in project work, commissioning of equipment, or managing vendors.</li><li>
Familiarity with regulatory expectations and good documentation practices in manufacturing environments.</li></ul> 
Work location and model 
This role is on-site at our Pakistan facility. Regular on-site presence is required to lead validation and commissioning activities. 
 
What we value 
We look for people who take responsibility, work openly with others, and focus on practical improvements. You will join a team that supports learning, growth and inclusion. We encourage clear, respectful communication and collaboration across teams. 
 
Ready to apply? 
If you are motivated to build your validation expertise and make an impact, we would like to hear from you. Please submit your CV and a short note explaining why this role interests you. We welcome candidates from varied backgrounds and encourage applications from all qualified people.
Why GSK? 
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
Contact information: 
You may apply for this position online by selecting the Apply now button.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</div>

Validation Engineer

Coatinks (Private) Limited

Department: Production.Production reporting to : Production/Plant ManagerLocation: DIPPL Factory.Purpose: To support the effective planning, execution, control, and documentation of production operations in order to ensure product conformity, timely order fulfilment, and compliance with ISO 9001:2015 requirements.Job Responsibilities:<ul><li>Plan and implement production schedules to meet customer requirements and delivery timelines.</li><li>Coordinate production activities across multiple product lines to ensure smooth workflow. Monitor and adjust production schedules as necessary to maximize efficiency and productivity.</li><li>Participate in capacity planning and line allocation to achieve production targets.</li><li>Oversee production operations to ensure compliance with quality standards.</li><li>Conduct regular product inspections to identify defects or deviations from specifications. Report and assist in managing nonconforming products, including segregation, rework, and documentation.</li><li>Maintain accurate production records to ensure batch traceability and data integrity.</li><li>Track inventory levels of raw materials and finished goods.</li><li>Liaise with procurement and logistics teams to ensure timely availability of required materials.</li><li>Optimize resource usage to minimize waste and control production costs.</li><li>Facilitate effective communication between Quality, Warehouse, Maintenance, and Planning teams to maintain seamless operations.</li><li>Support continuous improvement initiatives, including Lean, 5S, and Kaizen, to enhance overall efficiency.</li><li>Monitor production downtime and investigate root causes to reduce disruptions.</li><li>Assist in training production staff on SOPs, quality standards, and safety procedures. Support monitoring of team performance and provide constructive feedback to supervisors.</li><li>Ensure adherence to health and safety regulations and company policies.</li><li>Promote a safety-conscious culture and ensure compliance with safety protocols among production staff.</li></ul>Education Requirements:<ul><li>Bachelor&rsquo;s degree in Engineering, Industrial Manufacturing or relevant technical field.</li></ul>(Preferably BE/BS &ndash; Industrial, Mechanical, Chemical, or equivalent)Experience Requirements:<ul><li>2 to 5 years of experience in a production or manufacturing environment.</li><li>Experience in process control, quality inspection, or production planning is preferred. Good understanding of HSE culture and practices.</li><li>Strong communication and interpersonal and time management skills.</li><li>Experience with continuous improvement initiatives and ISO management system will be an advantage.</li></ul>Job Type: Full-timeWork Location: In person

Production Executive

Synergy Solutions

&middot; Proficiency with Creo (5.0) and AutoCAD 2017&middot; Knowledge and understanding of 3D CAD including modeling and drafting&middot; Knowledge of best practices in sheet metal industry&middot; Ability to come up with creative design solutions focusing on ease of manufacturability and assembly&middot; Ability to meet deadlines&middot; Strong communication skills&middot; Ability to collaborate and work with others to solve problems&middot; Create 2D electrical and civil drawings/layouts under supervision of lead engineer&middot; Work with engineering and manufacturing team to investigate and resolve problems with existing designs&middot; Create and update database of design records&middot; Participate in engineering and manufacturing design reviews to evaluate design concepts and make recommendationsEducation:DAE or diploma (Electrical/Mechanical)/certification in Creo 2017Experience:1-2 yearsLocation:Korangi Creek Industrial Park, Near Indus Hospital.Job Type: Full-timePay: Rs50,000.00 - Rs85,000.00 per monthWork Location: In person

CAD Designer

Khans International Brand (PVT) Limited

JOB DESCRIPTION: We are seeking a Mechanical Design Engineer with strong expertise in CAD design, Design for Manufacturability (DFM), installation and inspection of dynamic systems. The ideal candidate will contribute to the full product lifecycle from concept development through production, testing, and commissioning ensuring that designs meet performance, safety, and quality standards.QUALIFICATION: &#61672; Bachelor&rsquo;s degree in Mechanical Engineering. &#61672; 1-3 years of experience in mechanical design, preferably with dynamic or motion-based systems (e.g., robotics, machinery, automation, aerospace, or automotive). &#61672; Proficiency in SolidWorks, (experience with GD&amp;T and 2D drafting would be a plus). &#61672; Strong knowledge of DFM/DFA principles, materials, and manufacturing processes (machining, sheet metal, welding, etc.). &#61672; Hands-on experience with system installation, testing, and inspection in an industrial or R&amp;D setting. &#61672; Excellent communication skills and ability to collaborate in multidisciplinary teams.SKILLS: Dynamic Systems (CAD / DFM / Installation / Inspection)KEY RESPONSIBILITY &#61672;	Develop detailed 3D CAD models, assemblies, and manufacturing drawings for dynamic mechanical systems and components. &#61672;	Apply DFM principles to optimize designs for cost-effective manufacturing, assembly, and maintenance. &#61672;	Support installation, commissioning, and inspection of mechanical systems in the field or production environment. &#61672;	Conduct tolerance analysis, materials selection, and design verification to ensure compliance with performance and safety requirements. &#61672;	Collaborate with cross-functional teams (manufacturing, electrical, and controls) to ensure seamless system integration. &#61672;	Perform root cause analysis and support continuous improvement initiatives. &#61672;	Maintain documentation and revision control within the company&rsquo;s PLM or CAD data management system. LOCATION &#61672;	KarachiJob Type: Full-timeWork Location: In person

Assistant Manager - Mechanical

Explore 300+ Manufacturing engineer in Karachi this November. Find roles across top companies and apply now to boost your career.