quality control analyst

Nutrifactor Laboratories (Pvt) Limited

We are seeking a detail-oriented and motivated Quality Control Analyst to join our team at Nutrifactor.Qualifications: BS Chemistry or Pharm-D from a recognized universityExperience: 1 to 3 years in HPLC operationsResponsibilities:<ul><li>Conduct testing using HPLC and UV methods</li><li>Perform thorough RAW material testing to ensure compliance with quality standards</li><li>Execute finishing testing procedures for the final product</li><li>Monitor and analyses product samples to ensure they meet quality specifications</li><li>Conduct routine inspections and audits to identify areas for improvement</li><li>Ensure adherence to safety protocols and quality control regulations</li><li>Maintain accurate records of testing, inspections, and results</li><li>Identify and report any deviations from established quality standards</li><li>Assist in the development and implementation of quality control procedures</li><li>Provide training to lab technicians and other relevant staff</li><li>Collaborate with cross-functional teams to continuously improve quality processes</li></ul>Requirements:<ul><li>Strong knowledge of RAW material testing</li><li>Proficiency in finishing testing processes</li><li>Ability to handle multiple tasks simultaneously</li><li>Excellent organizational and multitasking skills</li><li>Effective written and verbal communication for preparing daily reports</li></ul>Job Type: Full-timeWork Location: In person

Quality Control Analyst

G NINE BIOCEUTICALS PVT LTD

GNINE is a third party manufacturing unit in beta-lactum (TABLET/DRY SYRUP &amp; DRY POWDER INJ).Requirement of Quality Control Analyst.Job Type: Full-timePay: ₹12,000.00 - ₹30,000.00 per monthWork Location: In person

Lonza

<div>QC Analyst IV &ndash; Environmental Monitoring
Location: Portsmouth, NH, USA.
As a QC Analyst IV, you are a Subject Matter Expert (SME) and a primary technical lead for the Environmental Monitoring team. This senior role is critical for maintaining the microbial control strategy of our multi-modal facility. You will be responsible for leading complex investigations, driving continuous improvement projects, and ensuring our EM program remains in a permanent state of compliance with global regulatory standards.
Schedule: Day Shift, Monday &ndash; Friday, 8:00 AM &ndash; 5:00 PM
What You&rsquo;ll Get<ul><li>
Technical Leadership: Act as a lead for the EM department, influencing site-wide quality culture and operational strategy.</li><li>
Audit Frontline: Represent the EM program as a Subject Matter Expert during internal and external regulatory inspections (FDA, EMA, etc.).</li><li>
Advanced Project Ownership: Lead the implementation of new technologies, such as rapid microbiological methods or paperless data systems.</li><li>
Comprehensive Benefits: Medical, dental, vision, 401(k), and performance-based incentives. Our full list of global benefits: lonza.com/careers/benefits.</li></ul>
What You&rsquo;ll Do<ul><li>
Technical SME Ownership: Serve as the technical lead for the site&rsquo;s EM and Utility monitoring programs. Provide high-level guidance on sampling plans, risk assessments, and the qualification of new cleanrooms.</li><li>
Complex Investigations: Lead and author high-complexity environmental excursion investigations. Utilize root cause analysis (RCA) tools to identify systemic issues and implement effective CAPAs.</li><li>
Data Trending &amp; Strategy: Perform advanced analysis of environmental and utility data. Identify long-term trends and present findings to site leadership and the Quality Council to drive proactive contamination control.</li><li>
Regulatory &amp; Audit Excellence: Prepare, review, and defend EM data and procedures during regulatory audits. Ensure all department SOPs and sampling protocols meet current Annex 1 and global cGMP expectations.</li><li>
Mentorship &amp; Coaching: Provide advanced technical training and mentorship to Level I, II, and III analysts. Foster a culture of technical excellence and &quot;Right First Time&quot; performance.</li><li>
Continuous Improvement: Identify and execute Lean Laboratory initiatives to increase efficiency, reduce lead times, and enhance data integrity across the EM program.</li><li>
Review &amp; Approval: Act as a final technical reviewer for complex laboratory records, validation protocols, and summary reports.</li></ul>
Who We&rsquo;re Looking For<ul><li>
Education: Bachelor&rsquo;s degree (BS) in a Life Sciences discipline (Microbiology, Biology, or related field) is required.</li><li>
Experience: 5&ndash;10 years of advanced experience in Quality Control Microbiology or Environmental Monitoring within a cGMP manufacturing environment is required.</li><li>
Technical Mastery: * Expert-level knowledge of cleanroom classifications (Grade A&ndash;D) and aseptic processing.<ul><li>
Deep understanding of global regulatory requirements (FDA, EMA, ICH) for environmental and utility monitoring.</li><li>
Proficiency in utilizing Laboratory Information Management Systems (LIMS) and data trending software.</li></ul></li><li>
Leadership Attributes: A proven track record of leading projects, managing timelines, and influencing cross-functional teams without direct authority.</li><li>
Communication: Exceptional technical writing skills and the ability to present complex scientific data clearly to senior management and auditors.</li></ul>
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone&rsquo;s ideas, big or small, have the potential to improve millions of lives, and that&rsquo;s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you&rsquo;re ready to help turn our customers&rsquo; breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to lead the standard of excellence in QC? Apply now.</div>

QC Analyst Level IV - Environmental Monitoring

Aria Systems India Pvt Ltd

<ul><li>Pharmaceutical &amp; Chemical Industry: Roles include Production Chemist, Quality Control (QC) Analyst, Analytical Chemist, and Drug Formulation Chemist.</li><li>Research &amp; Development (R&amp;D): Positions as Research Scientist or Lab Assistant in private firms or top government institutions like CSIR, DRDO, and BARC.</li><li>Quality Control &amp; Assurance: Ensuring product safety and regulatory compliance in food, beverages, cosmetics, and manufacturing industries.</li><li>Forensic &amp; Environmental Science: Working as a Forensic Scientist in crime labs or as a Toxicologist analyzing environmental samples.</li><li>Academia &amp; Education: Chemistry tutor, teacher, or lecturer (following NET/SET qualification).</li><li>Other Roles: Clinical Research Associate, Medical Coder, and Scientific Data Entry Specialist.</li></ul>Job Types: Full-time, Permanent, FresherPay: ₹18,086.00 - ₹32,445.44 per monthBenefits:<ul><li>Health insurance</li><li>Paid sick time</li><li>Paid time off</li><li>Provident Fund</li></ul>Work Location: In person

Bsc chemistry freshers

Global Recruiters

Job Advertisement: Lab Analyst &ndash; Cement IndustryLocation: HUB Plant, BaluchistanWe are looking for a competent and experienced Lab Analyst to join our Building Construction Chemical Manufacturing Plant at HUB, Baluchistan. The ideal candidate must have hands-on laboratory experience in the cement industry with strong knowledge of quality control and testing standards.Key Responsibilities:<ul><li>Perform routine laboratory testing of cement, clinker, raw mix, limestone, gypsum, and other raw materials.</li><li>Conduct physical and chemical tests including fineness, setting time, soundness, compressive strength, LOI, SO₃, and free lime.</li><li>Ensure all testing activities comply with ASTM, BS, and internal quality standards.</li><li>Maintain proper laboratory records, test reports, and quality documentation.</li><li>Operate, calibrate, and maintain laboratory equipment and instruments.</li><li>Coordinate with production and quality teams to ensure consistent product quality.</li><li>Follow safety, housekeeping, and environmental procedures within the laboratory.</li></ul>Qualification &amp; Experience:<ul><li>Bachelor&rsquo;s degree or Diploma in Chemistry, Chemical Engineering, or a related field.</li><li>Minimum 2&ndash;4 years of hands-on experience as a Lab Analyst in a cement manufacturing plant (mandatory).</li><li>Practical knowledge of cement testing methods and lab operations.</li></ul>Skills &amp; Competencies:<ul><li>Strong analytical and troubleshooting skills.</li><li>Attention to detail with accurate data recording.</li><li>Ability to work independently in a plant environment.</li><li>Good communication and coordination skills.</li></ul>We Offer:<ul><li>Career growth opportunities</li><li>Professional and safe working environment</li></ul>Job Type: Full-timePay: Rs50,000.00 - Rs60,000.00 per monthWork Location: In person

Lab Analyst (Cement Industry Experience) Male

SC Johnson

<div>
 SC JOHNSON IS A FIFTH-GENERATION FAMILY COMPANY BUILT ON THE SPIRIT OF OUR PEOPLE. We have been leading with purpose for over 130 years, building iconic brands that win the hearts and minds of consumers &ndash; such as Raid&reg;, Glade&reg;, Ziploc&reg; and more, in virtually every country around the world. Together, we are creating a better future &ndash; for the planet, for future generations and for every SCJ team member. Join our winning team of Wave Makers and Go Getters and help us write the next chapter in the SCJ story.
 
 
 
 Quality Analyst
 
 
 
 <ul>
 <li>
 Location: Cairo, Egypt
 </li>
 <li>
 Function: Quality
 
 
 </li>
 </ul>
 
 Overview
 
 
 
 As a Quality Analyst, you will help ensure SCJ products meet the highest standards of safety, compliance, and performance. You will support the deployment of quality management systems, continuous improvement initiatives, and world‑class best practices across laboratory and manufacturing processes. Your work will play an essential role in maintaining product integrity and protecting consumer trust.
 
 
 
 About The Role
 
 
 
 In this role, you will lead laboratory and on‑line quality control activities, support ISO and GLP compliance, and guide continuous improvement efforts across the site. You will collaborate with cross‑functional teams, conduct investigations, analyze data, and help drive improvements in product quality, processes, and supplier performance.
 
 
 
 About The Team/Department
 
 
 
 You will join the Quality function, reporting to the
 
 Manager, Quality
 
 . The team oversees product and raw‑material testing, regulatory compliance, internal audits, and quality system deployment to ensure SCJ&rsquo;s manufacturing operations deliver safe, compliant, high‑quality products to market.
 
 
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Deploy, maintain, and improve QMS standards, GLP practices, and compliance with local and international regulations
 </li>
 <li>
 Ensure all lab and online testing staff are trained, qualified, and following required procedures
 </li>
 <li>
 Oversee internal audits of equipment, testing methods, and documentation to ensure complete, compliant records
 </li>
 <li>
 Lead investigations of quality issues, conduct root‑cause analysis, execute CAPA, and manage release/hold decisions for raw materials and finished goods
 </li>
 <li>
 Manage qualification and validation activities for raw materials, products, processes, and lab equipment
 </li>
 <li>
 Drive supplier quality improvement; support audits, monitor KPIs, and collaborate on corrective actions
 </li>
 <li>
 Ensure accurate, consistent lab and online testing using statistical analysis to support process improvements
 </li>
 <li>
 Prepare quality performance reports highlighting KPIs, compliance, risks, and improvement initiatives
 
 
 </li>
 </ul>
 
 Experience You&rsquo;ll Bring
 
 
 
 <ul>
 <li>
 Early experience in Quality Control and Environment, Health &amp; Safety &mdash; ideally in aerosol manufacturing or FMCG
 </li>
 <li>
 Technical competency in quality operations and laboratory/test procedures.
 </li>
 <li>
 Degree in Chemical Engineering
 </li>
 <li>
 Effective at servicing internal and external stakeholders
 </li>
 <li>
 Knowledge of ISO 9001:2000, GLP, Pharmacopoeia, and chemical/micro testing procedures
 </li>
 <li>
 Ability to work across multidisciplinary teams, drive improvement, and deliver results
 
 
 </li>
 </ul>
 
 Behaviors You&rsquo;ll Need
 
 
 
 <ul>
 <li>
 Strong analytical mindset and attention to detail
 </li>
 <li>
 Proactive problem‑solver with a continuous improvement mindset
 </li>
 <li>
 Effective communicator and collaborator
 </li>
 <li>
 Adaptable and able to thrive in a fast‑paced manufacturing environment
 </li>
 <li>
 Commitment to safety, compliance, and quality excellence
 
 
 </li>
 </ul>
 
 Job Requirements
 
 
 
 <ul>
 <li>
 Full‑time position based onsite in Cairo, Egypt
 </li>
 <li>
 Not eligible for relocation
 </li>
 <li>
 Manufacturing environment&mdash;onsite work required
 </li>
 <li>
 Occasional overtime depending on business needs
 
 
 </li>
 </ul>
 
 Benefits
 
 
 
 <ul>
 <li>
 Comprehensive health and wellness benefits
 </li>
 <li>
 Employee discounts on SCJ products
 </li>
 <li>
 Learning &amp; development opportunities
 </li>
 <li>
 Supportive, inclusive, and safety‑focused work environment
 
 
 </li>
 </ul>
 
 Inclusion &amp; Diversity
 
 
 
 We&rsquo;re a global business, with people from every culture, ethnicity, race, religion, gender identity, sexual orientation, age, and ability. We recognize the breadth of human experience, and we work to celebrate it. It is our goal to build a diverse, inclusive, and supportive work environment where all people can thrive.
 
 
 We&rsquo;re committed to ongoing efforts that help us attract, hire, and retain diverse talent who want to build a positive, inclusive environment. Read more about our ongoing initiatives at https://jobs.scjohnson.com/inclusion.
 
 
</div>

Quality Analyst

<div>SC JOHNSON IS A FIFTH-GENERATION FAMILY COMPANY BUILT ON THE SPIRIT OF OUR PEOPLE. We have been leading with purpose for over 130 years, building iconic brands that win the hearts and minds of consumers &ndash; such as Raid&reg;, Glade&reg;, Ziploc&reg; and more, in virtually every country around the world. Together, we are creating a better future &ndash; for the planet, for future generations and for every SCJ team member. Join our winning team of Wave Makers and Go Getters and help us write the next chapter in the SCJ story.<h1 class="jobSectionHeader"> 
Quality Analyst
</h1><ul><li>Location: Cairo, Egypt</li><li>Function: Quality</li></ul><div></div><h2 class="jobSectionHeader">
Overview</h2><div>
As a Quality Analyst, you will help ensure SCJ products meet the highest standards of safety, compliance, and performance. You will support the deployment of quality management systems, continuous improvement initiatives, and world‑class best practices across laboratory and manufacturing processes. Your work will play an essential role in maintaining product integrity and protecting consumer trust.</div><div></div><h2 class="jobSectionHeader">
About the Role</h2><div>
In this role, you will lead laboratory and on‑line quality control activities, support ISO and GLP compliance, and guide continuous improvement efforts across the site. You will collaborate with cross‑functional teams, conduct investigations, analyze data, and help drive improvements in product quality, processes, and supplier performance.</div><div></div><h2 class="jobSectionHeader">
About the Team/Department</h2><div>
You will join the Quality function, reporting to the Manager, Quality. The team oversees product and raw‑material testing, regulatory compliance, internal audits, and quality system deployment to ensure SCJ&rsquo;s manufacturing operations deliver safe, compliant, high‑quality products to market.</div><div></div><h2 class="jobSectionHeader">
Responsibilities:</h2><ul><li>Deploy, maintain, and improve QMS standards, GLP practices, and compliance with local and international regulations</li><li>Ensure all lab and online testing staff are trained, qualified, and following required procedures</li><li>Oversee internal audits of equipment, testing methods, and documentation to ensure complete, compliant records</li><li>Lead investigations of quality issues, conduct root‑cause analysis, execute CAPA, and manage release/hold decisions for raw materials and finished goods</li><li>Manage qualification and validation activities for raw materials, products, processes, and lab equipment</li><li>Drive supplier quality improvement; support audits, monitor KPIs, and collaborate on corrective actions</li><li>Ensure accurate, consistent lab and online testing using statistical analysis to support process improvements</li><li>Prepare quality performance reports highlighting KPIs, compliance, risks, and improvement initiatives</li></ul><div></div><h2 class="jobSectionHeader">
Experience You&rsquo;ll Bring:</h2><ul><li>Early experience in Quality Control and Environment, Health &amp; Safety &mdash; ideally in aerosol manufacturing or FMCG</li><li>Technical competency in quality operations and laboratory/test procedures.</li><li>Degree in Chemical Engineering</li><li>Effective at servicing internal and external stakeholders</li><li>Knowledge of ISO 9001:2000, GLP, Pharmacopoeia, and chemical/micro testing procedures</li><li>Ability to work across multidisciplinary teams, drive improvement, and deliver results</li></ul><div></div><h2 class="jobSectionHeader">
Behaviors You&rsquo;ll Need:</h2><ul><li>Strong analytical mindset and attention to detail</li><li>Proactive problem‑solver with a continuous improvement mindset</li><li>Effective communicator and collaborator</li><li>Adaptable and able to thrive in a fast‑paced manufacturing environment</li><li>Commitment to safety, compliance, and quality excellence</li></ul><div></div><h2 class="jobSectionHeader">
Job Requirements:</h2><ul><li>Full‑time position based onsite in Cairo, Egypt</li><li>Not eligible for relocation</li><li>Manufacturing environment&mdash;onsite work required</li><li>Occasional overtime depending on business needs</li></ul><div></div><h2 class="jobSectionHeader">
Benefits:</h2><ul><li>Comprehensive health and wellness benefits</li><li>Employee discounts on SCJ products</li><li>Learning &amp; development opportunities</li><li>Supportive, inclusive, and safety‑focused work environment</li></ul>
#LI-AP2 
Inclusion &amp; Diversity
We&rsquo;re a global business, with people from every culture, ethnicity, race, religion, gender identity, sexual orientation, age, and ability. We recognize the breadth of human experience, and we work to celebrate it. It is our goal to build a diverse, inclusive, and supportive work environment where all people can thrive.
We&rsquo;re committed to ongoing efforts that help us attract, hire, and retain diverse talent who want to build a positive, inclusive environment. Read more about our ongoing initiatives at https://jobs.scjohnson.com/inclusion.</div>

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Bsc chemistry freshers

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