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sqa engineer

production manager

design engineer

head of qc and r&d

head of qc and r d

Sika

<div>
 
 Company Description
 
 
 
 Sika is a specialty chemicals company with a globally leading position in the development and production of systems and products for bonding, sealing, damping, reinforcing, and protection in the building sector and industry. Sika has subsidiaries in 103 countries around the world, produces in over 400 factories, and develops innovative technologies for customers worldwide. In doing so, it plays a crucial role in enabling the transformation of the construction and transportation industries toward greater environmental compatibility. In 2024, Sika&rsquo;s around 33,000 employees generated annual sales of CHF 11.76 billion.
 
 
 Sika Pakistan (Pvt) Limited is a subsidiary of Sika AG - Switzerland and started its operations in 2010 on 100th anniversary of Sika worldwide.
 
 
 With an aim to become number one construction chemical company in Pakistan, Sika Pakistan opened its head office in Lahore with regional offices in Karachi, Islamabad and Faisalabad. Simultaneously, Sika Pakistan also launched its manufacturing facility in Lahore during the first year of the start of operations in Pakistan to facilitate its customer needs.
 
 
 
 Job Description
 
 
 
 
 Job Summary:
 
 
 
 We are seeking a highly skilled and strategic Head of QC and R&amp;D to lead the overall quality control and product development functions, ensuring all products meet internal standards and external regulations. The role is responsible for maintaining consistent product quality, driving innovation through R&amp;D, and supporting cross-functional teams in product improvement and troubleshooting.
 
 
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Lead quality control operations, ensuring raw materials and finished goods comply with defined specifications and industry standards.
 </li>
 <li>
 Drive R&amp;D initiatives for new product development and continuous improvement of existing formulations.
 </li>
 <li>
 Liaise with production, procurement, and technical teams to resolve quality-related issues and implement preventive actions.
 </li>
 <li>
 Oversee lab testing protocols, calibration, documentation, and reporting systems.
 </li>
 <li>
 Lead and mentor the QC &amp; R&amp;D teams, ensuring alignment with organizational goals.
 </li>
 <li>
 Evaluate new raw materials, support cost-optimization efforts, and manage technical trials.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Bachelor of Master&rsquo;s degree in Chemistry / Chemical Engineering / Materials Science.
 </li>
 <li>
 10&ndash;12 years of experience in Quality Control and/or R&amp;D, preferably in construction chemicals or related industries.
 </li>
 <li>
 In-depth knowledge of testing standards (ASTM, EN, BS), chemical compatibility, and formulation chemistry.
 </li>
 <li>
 Strong leadership, analytical, and problem-solving skills.
 </li>
 </ul>
</div>

Head of QC and R&D

Sika Corporation

<div>Our goals - Your path
<div>Job Summary:
We are seeking a highly skilled and strategic Head of QC and R&amp;D to lead the overall quality control and product development functions, ensuring all products meet internal standards and external regulations. The role is responsible for maintaining consistent product quality, driving innovation through R&amp;D, and supporting cross-functional teams in product improvement and troubleshooting.
Key Responsibilities:<ul><li>
Lead quality control operations, ensuring raw materials and finished goods comply with defined specifications and industry standards.</li><li>
Drive R&amp;D initiatives for new product development and continuous improvement of existing formulations.</li><li>
Liaise with production, procurement, and technical teams to resolve quality-related issues and implement preventive actions.</li><li>
Oversee lab testing protocols, calibration, documentation, and reporting systems.</li><li>
Lead and mentor the QC &amp; R&amp;D teams, ensuring alignment with organizational goals.</li><li>
Evaluate new raw materials, support cost-optimization efforts, and manage technical trials.</li></ul></div>
Your expertise - Our strength
<div><ul><li>Bachelor of Master&rsquo;s degree in Chemistry / Chemical Engineering / Materials Science.</li><li>
10&ndash;12 years of experience in Quality Control and/or R&amp;D, preferably in construction chemicals or related industries.</li><li>
In-depth knowledge of testing standards (ASTM, EN, BS), chemical compatibility, and formulation chemistry.</li><li>
Strong leadership, analytical, and problem-solving skills.</li></ul></div>
<div></div><h3 class="jobSectionHeader">About Sika</h3>
<div>Sika is a specialty chemicals company with a globally leading position in the development and production of systems and products for bonding, sealing, damping, reinforcing, and protection in the building sector and industry. Sika has subsidiaries in 103 countries around the world, produces in over 400 factories, and develops innovative technologies for customers worldwide. In doing so, it plays a crucial role in enabling the transformation of the construction and transportation industries toward greater environmental compatibility. In 2024, Sika&rsquo;s around 33,000 employees generated annual sales of CHF 11.76 billion.
Sika Pakistan (Pvt) Limited is a subsidiary of Sika AG - Switzerland and started its operations in 2010 on 100th anniversary of Sika worldwide.
With an aim to become number one construction chemical company in Pakistan, Sika Pakistan opened its head office in Lahore with regional offices in Karachi, Islamabad and Faisalabad. Simultaneously, Sika Pakistan also launched its manufacturing facility in Lahore during the first year of the start of operations in Pakistan to facilitate its customer needs.</div></div>

Quick Food industries Pvt. Ltd

Mon Salwa (Quick Food Industries Pvt. Ltd.) is hiring a Head &ndash; Quality Control &amp; Assurance to lead our Quality team.Location: Sundar Industrial Estate, LahoreKey Responsibilities:<ul><li>Ensure consistent product quality and regulatory compliance by implementing robust quality standards across all production stages.</li><li>Oversee the execution and continuous improvement of QA/QC systems in line with national and international food safety standards.</li><li>Lead investigations of quality issues and non-conformities and implement effective Corrective and Preventive Actions (CAPA).</li><li>Manage internal and external audits, ensuring the facility remains audit-ready and meets all certification and legal requirements.</li><li>Work closely with cross-functional teams including Production, R&amp;D, and Procurement to resolve quality concerns and optimize efficiency.</li></ul>Qualification: Master&rsquo;s degree in food science, Biotechnology, or a related field from a recognized institution.Relevant certifications in food safety/quality systems are preferred.Experience:10&ndash;12 years of progressive experience in Quality Control &amp; Assurance, with at least 7 years in a managerial role within frozen food manufacturing.Job Type: Full-timeWork Location: In person

Head – Quality Control & Assurance(FrozenFood)

Pacific Pharmaceuticals

Pacific Pharmaceuticals has been producing and marketing quality pharmaceuticals strictly in compliance with GMP Rules and Regulations and WHO Standards, for more than three decades and serving the nation with world class medicines.Responsibilities:<ul><li>Perform analysis of raw materials, in-process samples, finished products, and stability samples using instruments like HPLC, GC, UV-Vis, FTIR, etc.</li><li>Prepare and review analytical reports and related documentation in compliance with cGMP, GLP, and regulatory guidelines.</li><li>Conduct method validation, method transfer, and routine calibrations.</li><li>Investigate out-of-specification (OOS) and out-of-trend (OOT) results, deviations, and support CAPA implementation.</li><li>Ensure timely completion of all assigned QC activities and contribute to batch release processes.</li><li>Collaborate with production, QA, R&amp;D, and regulatory departments to ensure consistent quality and regulatory compliance.</li><li>Assist in audits (internal/external) and implement corrective actions when necessary.</li></ul>Requirements:<ul><li>Education: Pharm-D / M. Sc (Analytical Chemistry, Pharmaceutical Chemistry, or equivalent)</li><li>Experience: Minimum 4-5 years in QC within a pharmaceutical manufacturing</li><li>Strong knowledge of analytical techniques and regulatory requirements.</li><li>Proficient in handling analytical instruments and software.</li><li>Excellent documentation and reporting skills</li><li>Strong attention to detail, problem-solving, and time management skills</li></ul>Job Type: Full-timeWork Location: In person

Quality Control Analyst (Executive)

Pharmaceutical Lahore

Job descriptionCompany DescriptionWe suggest you enter details here.Role DescriptionThis is a full-time on-site role for a Deputy Manager Quality Control (QC), located in Lahore. The Deputy Manager QC will oversee and manage quality control processes, ensure compliance with industry standards and regulations, and conduct quality audits. The role involves leading a team of quality control analysts, developing and implementing quality control systems, and ensuring that all products meet the required quality standards. Additionally, the Deputy Manager QC will coordinate with the production and R&amp;D departments to address quality issues and implement corrective actions.Qualifications<ul><li>Experience 8 to 10 years in Quality Control and Quality Assurance</li><li>Strong knowledge of industry standards and regulatory requirements</li><li>Team management and leadership skills</li><li>Excellent problem-solving and analytical skills</li><li>Effective communication and interpersonal skills</li><li>Bachelor's degree in Pharmacy, Chemistry, or related field (Master's preferred)</li><li>Experience in the pharmaceutical industry is highly desirable</li><li>Proficiency in using quality control software and tools</li></ul>Job Type: Full-timeWork Location: In person

Deputy Manager Quality Control (QC)

Interwood Mobel

<div>The Sr. Manager/Manager of Production is responsible for managing all production activities in a cost-effective way, ensuring
efficient processes, and maintaining high standards in the manufacturing of KDW, Home and Office Furniture,
NPD, Mocks and project-related products.
Key Responsibilities:<ul>
<li>Plan and execute monthly and quarterly production schedules in line with business targets, giving priority to urgent, complaint-related, mock, NPD, and NPD Zero Batch orders.
</li><li>Ensure timely achievement of production targets for both stock and custom orders while meeting delivery commitments.
</li><li>Coordinate with R&amp;D, QC, and Technical teams to obtain necessary approvals for NPD Zero Batch items before initiating large-scale production.
</li><li>Lead the implementation of a Capacity Resource Planning system in partnership with Technical and IT teams to enhance productivity and optimize operational efficiency.
</li><li>Manage day-to-day production activities to ensure compliance with quality standards and adherence to scheduled production timelines.
</li><li>Introduce and oversee the use of project management tools and AI technologies to automate workflows, streamline operations, and reduce manual interventions.
</li><li>Monitor and control production costs, ensuring alignment with budgeted targets and maintaining operations within break-even thresholds.
</li><li>Implement strategies to reduce rework and wastage, ensuring adherence to QC benchmarks and improving overall production throughput.
</li><li>Collaborate with the IT department to integrate AI-driven dashboards and reporting tools for real-time performance monitoring and decision-making.
</li><li>Work closely with the Head of Technical to ensure smooth onboarding of new orders into the production cycle without delays or quality issues.
</li><li>Foster a culture of continuous improvement and leadership development through structured succession planning across all production units.</li>
</ul>Requirements<ul>
<li>Bachelor's degree in Industrial Engineering, Mechanical Engineering, or a related field; MBA or Master's in Operations/Production Management is preferred.</li>
<li>Minimum 10-12 years of experience in production planning and operations, ideally within a manufacturing or industrial environment.</li>
<li>Proficiency in production workflows, capacity planning, lean manufacturing, and ERP systems; familiarity with AI tools and project management software is a strong advantage.</li>
<li>Strong analytical skills with the ability to evaluate production data, manage budgets, and drive process optimization while ensuring quality.</li>
<li>Effective leadership and team management capabilities, with experience in cross-functional collaboration and talent development.</li>
<li>Proven track record of implementing automation solutions and digital tools to streamline operations and minimize manual intervention.</li>
</ul>Benefits<ul>
<li>Medical Insurance</li>
<li>Provident Fund</li>
<li>EOBI</li>
<li>Paid Leaves</li>
<li>Easy loan &amp; advance facility</li>
<li>Incentive Scheme as per organizational policy</li></ul></div>

Senior Manager Production

Sehat Medical Devices Pvt Ltd

<div>
 
 
 QC Manager
 
 
 
 
 Location:
 
 Sundar Industrial Estate, Lahore, Pakistan
 
 
 
 Department:
 
 Quality Control
 
 
 
 
 
 
 Position Overview
 
 
 
 The QC Manager will be responsible for overseeing all quality control operations at Sehat Medical Devices Pvt Ltd (SMD), ensuring products meet international quality standards, regulatory requirements, and customer specifications. This role requires deep technical expertise in medical device manufacturing, particularly syringes, infusion sets, and other disposables, as well as leadership skills to manage a multidisciplinary QC team.
 
 
 
 
 
 
 Key Responsibilities
 
 
 
 
 Quality Control Operations
 
 
 <ul>
 <li>
 Lead all QC activities from raw material inspection to final product release.
 </li>
 <li>
 Implement and maintain quality control procedures in compliance with
 
 ISO 13485, ISO 10993, ISO 9001, GMP, WHO PQ
 
 and
 
 DRAP Medical Device Rules 2017
 
 .
 </li>
 <li>
 Ensure inspection and testing are carried out at all stages&mdash;incoming, in-process, and final&mdash;according to
 
 ISO 7886-1, ISO 8536, ISO 7864
 
 , and other relevant standards.
 </li>
 <li>
 Oversee microbiological, chemical, and mechanical testing in accordance with SMD&rsquo;s validated protocols.
 </li>
 <li>
 Manage product traceability systems, including
 
 batch number verification, retention samples, and documentation
 
 .
 </li>
 </ul>
 
 
 Compliance &amp; Regulatory
 
 
 <ul>
 <li>
 Ensure full compliance with
 
 DRAP regulations, ISO standards, and international customer requirements
 
 .
 </li>
 <li>
 Prepare and maintain QC records for regulatory audits, customer inspections, and internal reviews.
 </li>
 <li>
 Support certification processes for
 
 ISO 13485 Notified Body audit, WHO Prequalification, CE Marking, and FDA 510(k)
 
 .
 </li>
 <li>
 Liaise with regulatory bodies for inspections, queries, and product approvals.
 </li>
 </ul>
 
 
 Lab Management
 
 
 <ul>
 <li>
 Supervise QC laboratory operations, ensuring calibration and maintenance of equipment such as Universal Testing Machines, Leak Testers, UV-Vis spectrophotometers, GC, AAS, and microbiology lab instruments.
 </li>
 <li>
 Oversee procurement and qualification of new QC instruments.
 </li>
 <li>
 Establish lab safety protocols and training for staff.
 </li>
 </ul>
 
 
 Team Leadership
 
 
 <ul>
 <li>
 Manage, train, and mentor the QC team, including inspectors, lab technicians, and microbiologists.
 </li>
 <li>
 Set departmental KPIs and monitor performance against targets.
 </li>
 <li>
 Foster a culture of continuous improvement and root cause problem-solving.
 </li>
 </ul>
 
 
 Investigation and Continuous Improvement
 
 
 <ul>
 <li>
 Lead product non-conformance investigations, CAPA (Corrective and Preventive Actions), and deviation handling.
 </li>
 <li>
 Work closely with Production, QA, and R&amp;D teams to resolve quality issues.
 </li>
 <li>
 Implement statistical process control (SPC) and other data-driven quality improvement tools.
 </li>
 <li>
 Recommend process changes to reduce defects, improve yields, and ensure zero-compromise on product safety.
 </li>
 </ul>
 
 
 
 <ul>
 <li>
 
 QUALIFICATIONS
 
 </li>
 <li>
 Bachelor&rsquo;s or Master&rsquo;s degree in Biomedical Engineering, Pharmacy, Bio Technology etc
 </li>
 <li>
 8+ years of experience in QC, preferably in medical device manufacturing.
 </li>
 <li>
 In-depth knowledge of ISO 13485, ISO 10993, ISO 7886-1, ISO 7864, and relevant product standards.
 </li>
 <li>
 Experience with GMP, regulatory audits, and third-party certifications.
 </li>
 <li>
 Strong analytical skills with hands-on experience in laboratory testing and inspection methods.
 </li>
 <li>
 Proficiency in MS Office, ERP/Quality Management Systems
 </li>
 </ul>
 
 
 
 
 Interested candidates are encouraged to apply at hr@sehat.ltd or through the easy apply button on linkedin
 
</div>

QC Manager - Medical Devices

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