lab analyst

<div>
 
 Site Name:
 
 Pakistan - Sindh - Karachi
 
 
 
 Posted Date:
 
 Mar 2 2026
 
 
 
 Job Purpose
 
 
 
 Ensure Quality Compliance of Products / Materials at various stages of testing (including raw material, intermediate and finished product &amp; stability testing) to fulfill regulatory and GMP/GLP requirements, coordinate for the fulfillment of GMP compliance and various quality requirements as per GQMPs and GQPs and manage the product validation program in line with GMP requirements.
 
 
 
 Key Responsibilities
 
 
 
 
 <ul>
 <li>
 Receiving and analysis of representative samples of Finished product, Intermediate product, Raw material, Stability, Trace/CLV for timely release by Lab operations.
 </li>
 <li>
 Release of Finished product, intermediate and Raw material in LIMS &amp; SAP.
 </li>
 <li>
 Analysis of Stability or Validation samples and interpretation of results
 </li>
 <li>
 Support in the management of Stability Program for timely assure the Stability.
 </li>
 <li>
 Inventory Maintenance, handling and disposition of Reference Standards after expiry.
 </li>
 <li>
 Follow GMP and safety requirement of Laboratory and participate in Various EHS activities.
 </li>
 <li>
 Participate in the testing of new products and product development.
 </li>
 <li>
 Conduct and participate in Mandatory OJT/ GMP training sessions.
 </li>
 <li>
 Support in preparation and revision of existing SOPS, Testing standards and Testing Methods to set standards as per GMP compliance.
 </li>
 <li>
 Demonstrate proficiency in standard computer software for the use of Analytical Instruments.
 </li>
 <li>
 Destruction of the product material left after analysis and managing the destruction of hazardous chemical waste.
 
 
 
 </li>
 </ul>
 
 Education, Experience &amp; Skills
 
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s or Master&rsquo;s degree in Pharm D, Applied Chemistry, Chemistry, Biochemistry, Analytical Chemistry, industrial engineering, or a related science discipline.
 </li>
 <li>
 0 to 2 years of relevant laboratory experience in quality control, analytical testing, or a similar regulated environment.
 </li>
 <li>
 Practical experience or familiarity with common analytical techniques and instruments such as HPLC, GC, UV-visible spectrophotometry or equivalent.
 </li>
 <li>
 Basic computer skills including MS Office and willingness to learn LIMS (Laboratory Information Management System) and SAP or other ERP systems.
 </li>
 <li>
 Clear written and verbal communication skills and ability to work collaboratively in diverse teams.
 </li>
 <li>
 Understanding of good laboratory and good manufacturing practices and commitment to following procedures.
 </li>
 <li>
 Exposure to method validation, method transfer, or finished product testing.
 </li>
 <li>
 Experience supporting investigations, root cause analysis and corrective actions.
 </li>
 <li>
 Knowledge of quality management systems and document control processes.
 </li>
 <li>
 Strong attention to detail, organisation and basic data calculation skills.
 
 
 
 </li>
 </ul>
 
 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>

Lab Analyst

University of Massachusetts

<div>Overview:
<div>
POSITION SUMMARY:
</div><div>Under the direct supervision of Lab Management, the Lab Analyst I performs laboratory assays for the timely detection of newborn disorders. The Lab Analyst I maintains competency in high complexity testing (as defined by CLIA) in all laboratory methodologies of the section. The analyst performs other related laboratory tasks in support of laboratory management. Responsibilities include careful adherence to established laboratory protocols, or specific directives of appropriate laboratory managers. This is an entry level laboratory position that will receive a high level of direction and supervision to perform assigned work.</div>
Responsibilities:
<div>
ESSENTIAL FUNCTIONS:</div><ul><li>
Performs laboratory assays (clinical or research) with appropriate documentation, as an integral member of the section&rsquo;s laboratory analysts, following validated protocols.</li><li>
Follows established safety and privacy protocols.</li><li>
Assists management in the performance and documentation of laboratory activities for the technical development, validation, performance and troubleshooting of laboratory assays (both laboratory-developed tests as well as kit assays) used in the screening procedures.</li><li>
Assists management in laboratory activities for validation, troubleshooting the performance of and management of instrumentation used in the screening procedures.</li><li>
Assists management in laboratory activities for validation, troubleshooting and monitoring of the instrumentation relationships with LIMS.</li><li>
Works as an integral team member as needed in the preparation and validation of reagents, materials and kits used in the laboratory.</li><li>
Contributes data for laboratory documentation of quality assurance, quality control, and competency data in accordance with Program policies and CLIA requirements.</li><li>
Perform other duties as required.</li></ul>
Qualifications:
<div>
REQUIRED QUALIFICATIONS:</div><ul><li>
Bachelor&rsquo;s degree in chemical, life or clinical sciences; or equivalent</li><li>
0-2 years of experience including previous laboratory experience</li><li>
Must satisfy CLIA requirements for high complexity testing</li><li>
Experience with standard concepts, practices, and procedures within the clinical laboratory</li><li>
Good communication and organizational skills, with focus on detail and orderliness</li><li>
Ability to perform laboratory procedures as assigned once trained, with great care and attention</li><li>
Strong interpersonal skills</li><li>
Experience with productivity software (Excel, Word, Access)</li><li>
Flexibility in work schedule as required by laboratory section (i.e., weekend and holiday rotations).</li></ul> 

Additional Information:
<div>
PREFERRED QUALIFICATIONS:</div><ul><li>
Experience with standard concepts, practices, and procedures within the clinical laboratory</li></ul></div>

Lab Analyst I NENSP

Marc

<div>MARC for Medical Services and Scientific Research is an integrative research center that aims to advance science by conducting research in interdisciplinary disease areas. Our goal is to conduct high-priority and ethical basic, preclinical and clinical research, bridging the gap between science and community to improve health and quality of life.
MARC is looking to have an experienced candidate for Bioequivalence In-vivo Lab Analyst<ul><li>
Key responsibilities:</li><li><ul><li>
Perform bioanalytical method development, validation, and in-vivo sample analysis using LC&ndash;MS/MS in compliance with SOPs, GLP, and regulatory guidelines.</li><li>
Ensure proper equipment calibration, maintenance, and documentation in accordance with GLP.</li><li>
Prepare and process samples and reagents while ensuring data accuracy, traceability, and integrity per ALCOA+ principles.</li></ul></li></ul> 
Requirements 
<ul><li><ul><li>
Bachelor&rsquo;s degree in science or pharmacy</li><li>
1&ndash;3 years of experience in a bioanalytical laboratory.</li><li>
At least one year of hands-on experience with LC&ndash;MS/MS and bioanalytical method development and validation</li><li>
Ability to perform routine bioanalytical analysis.</li></ul></li></ul></div>

Bioequivalence In-vivo Lab Analyst

MARC

<div>
 MARC for Medical Services and Scientific Research is an integrative research center that aims to advance science by conducting research in interdisciplinary disease areas. Our goal is to conduct high-priority and ethical basic, preclinical and clinical research, bridging the gap between science and community to improve health and quality of life.
 
 
 MARC is looking to have an experienced candidate for
 
 Bioequivalence In-vivo Lab Analyst
 
 
 
 <ul>
 <li>
 Key responsibilities:
 </li>
 <li>
 Perform bioanalytical method development, validation, and in-vivo sample analysis using LC-MS/MS in compliance with SOPs, GLP, and regulatory guidelines
 </li>
 <li>
 Ensure proper equipment calibration, maintenance, and documentation in accordance with GLP
 </li>
 <li>
 Prepare and process samples and reagents while ensuring data accuracy, traceability, and integrity per ALCOA+ principles.
 
 
 </li>
 </ul>
 
 Requirements
 
 
 
 <ul>
 <li>
 Bachelor's degree in science or pharmacy
 </li>
 <li>
 1-3 years of experience in a bioanalytical laboratory
 </li>
 <li>
 At least one year of hands-on experience with LC-MS/MS and bioanalytical method development and validation
 </li>
 <li>
 Ability to perform routine bioanalytical analysis
 </li>
 </ul>
</div>

FIPCO

MUST HAVE STRONG KNOWLEDGE OF STANDARDS, QUALITY ASSURANCE,COMPLIANCE, MICROBIAL &amp; CHEMICAL TESTING OF FOOD INGREDIENTS ANDPRODUCTS &amp; DOCUMENTATION.HANDS-ON EXPERIENCE WITH LAB EQUIPMENT AND PROCEDURESGOOD UNDERSTANDING OF FOOD QUALITY AND SAFETY STANDARDSCANDIDATES LIVING NEARBY KORANGI WILL BE PREFERRED.EXPERIENCEFresh-1 year of experience in QA, Compliance, QualityControl, Baking &amp; RnDOnly female candidates based in Karachi may apply.Job Type: Full-timePay: Rs30,000.00 - Rs50,000.00 per monthWork Location: In person

JUNIOR LAB ANALYST

Tech Pinacle Innovation Pvt Ltd

Job Title: PathNet &amp; Lab Interfaces Analyst (LIS Integration Specialist)Role OverviewThe PathNet &amp; Lab Interfaces Analyst is responsible for supporting, optimizing, and integrating Laboratory Information System (LIS) workflows, including PathNet, across enterprise healthcare environments. This role ensures accurate and efficient laboratory order processing, specimen tracking, result reporting, and seamless system interoperability using HL7 interfaces and middleware solutions.The ideal candidate has strong experience in LIS workflows, interface troubleshooting, lab analytics, and healthcare integration standards, with the ability to collaborate effectively with laboratory staff, clinical teams, and IT stakeholders.Key ResponsibilitiesLIS Workflow Management (PathNet)<ul><li>Support and optimize end-to-end LIS workflows, including:</li><li>Order entry and accessioning</li><li>Specimen collection and tracking</li><li>Testing and result validation</li><li>Result reporting and distribution</li><li>Configure test catalogs, reference ranges, and result rules.</li><li>Maintain system dictionaries, order codes, and test mappings.</li><li>Support laboratory compliance and regulatory requirements.</li></ul>HL7 Interface Management &amp; Troubleshooting<ul><li>Monitor and troubleshoot HL7 interfaces between LIS, EMR, middleware, and external systems.</li><li>Analyze inbound/outbound HL7 messages (ADT, ORM, ORU, etc.).</li><li>Resolve interface errors, message mapping issues, and data discrepancies.</li><li>Coordinate with interface engine teams and vendors for issue resolution.</li><li>Support new interface builds, upgrades, and system migrations.</li></ul>Middleware &amp; Instrument Integration<ul><li>Support laboratory middleware tools for instrument connectivity.</li><li>Maintain analyzer interfaces and device communication workflows.</li><li>Troubleshoot instrument result transmission and data integrity issues.</li><li>Validate result routing and reflex testing logic.</li></ul>Lab Analytics &amp; Reporting<ul><li>Develop and maintain laboratory analytics dashboards and reports, including:</li><li>Turnaround time (TAT)</li><li>Test volumes</li><li>Quality indicators</li><li>Productivity metrics</li><li>Analyze lab performance trends and recommend workflow improvements.</li><li>Support operational and financial reporting needs.</li></ul>Production Support &amp; Incident Management<ul><li>Provide Level 2/3 support for PathNet and lab interfaces.</li><li>Perform root cause analysis for system or interface failures.</li><li>Participate in change management and release validation.</li><li>Ensure minimal disruption to laboratory operations.</li></ul>Compliance &amp; Data Governance<ul><li>Support HIPAA compliance and patient data security.</li><li>Maintain audit logs and validation documentation.</li><li>Assist in regulatory readiness and accreditation requirements (e.g., CAP, CLIA).</li></ul>Required Qualifications<ul><li>Bachelor&rsquo;s degree in Healthcare Informatics, Information Systems, Laboratory Science, or related field (or equivalent experience).</li><li>5+ years of experience supporting LIS environments (PathNet preferred).</li><li>Strong knowledge of laboratory workflows.</li><li>Hands-on experience troubleshooting HL7 interfaces.</li><li>Experience with lab middleware and instrument integrations.</li><li>Familiarity with healthcare integration standards (HL7, TCP/IP).</li><li>Strong analytical and troubleshooting skills.</li><li>Ability to collaborate with lab operations and IT teams.</li></ul>Preferred Qualifications<ul><li>Experience with enterprise interface engines (e.g., Cloverleaf, Rhapsody, Mirth).</li><li>Experience in multi-site or hospital laboratory networks.</li><li>Knowledge of SQL for reporting and data validation.</li><li>Certification in healthcare IT or laboratory informatics (preferred).</li></ul>Key Competencies<ul><li>LIS Workflow Optimization</li><li>HL7 Interface Troubleshooting</li><li>Middleware &amp; Instrument Integration</li><li>Laboratory Analytics &amp; Reporting</li><li>Healthcare Data Standards</li><li>Incident &amp; Change Management</li><li>Regulatory Compliance Support</li><li>Cross-Functional Collaboration</li></ul>Job Types: Full-time, PermanentPay: ₹550,768.19 - ₹1,834,611.95 per yearWork Location: Hybrid remote in Noida

PathNet & Lab Interfaces Analyst (LIS Integration Specialist)

ENVIRODESIGNS ECO LABS

Analyst / Senior Analyst (Instrumentation Section) required for an NABL accredited testing lab in Kochi. The person should be well versed in analysis, method validation, verification, Measurement Uncertainty calculations of food, water, environmental samples etc., including independent handling of instrument LCMSMS.Operational knowledge of instruments like GCMSMS, ICP MS, IC, HPLC, FTIR etc. and wet lab analysis experience preferred. M.Sc. / B.Sc. Chemistry candidates from Kerala with more than 2 years experience in NABL accredited testing labs may apply.Job Type: Full-timePay: ₹15,000.00 - ₹30,000.00 per monthApplication Question(s):<ul><li>Please inform your current and expected salary per month.</li></ul>Experience:<ul><li>Instrumentation analysis: 2 years (Preferred)</li></ul>Work Location: In person

Analyst (Instrumentation Section) - LCMSMS

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Lab Analyst

Lab Analyst I NENSP

Bioequivalence In-vivo Lab Analyst

Bioequivalence In-vivo Lab Analyst

JUNIOR LAB ANALYST

PathNet & Lab Interfaces Analyst (LIS Integration Specialist)

Analyst (Instrumentation Section) - LCMSMS