Lab Analyst

GSK; Karachi Division; On-site; PKR 600,000 - 900,000; Full time

Job summary

GSK invites applications for a Lab Analyst to ensure quality compliance across finished products, raw materials, and stability testing in a regulated lab environment. The role emphasizes GMP/GLP adherence, method verification, and data integrity while supporting EHS initiatives and training programs.

Candidate should hold a bachelor’s degree in chemistry or related discipline with 1–2 years of pharma QC experience; proficiency in LIMS/SAP and instrument software is preferred.

Qualifications

• Bachelor’s in applied chemistry, chemistry, industrial chemistry or related discipline.
• 1–2 years in a pharmaceutical QC laboratory or similar regulated environment.
• Fundamental understanding of pharmaceutical quality control, analytical techniques and GMP/GLP principles.
• Hands-on experience with analytical instruments and stability/validation testing.
• Familiarity with EHS requirements for laboratory operations and hazardous waste management.
• Continuous improvement mindset and willingness to contribute to SOP/method updates and quality initiatives.
• Proficiency in standard computer applications; willingness to learn LIMS/SAP and instrument software.
• Effective communication skills and ability to work collaboratively within cross-functional teams.

Responsibilities

• Receive and analyse representative samples of finished product, intermediate product, raw materials, stability and trace/CLV to enable timely release by Lab Operations.
• Perform routine and non-routine testing, including stability and validation samples, interpret results and escalation OOS/OOT in line with GMP and site procedures.
• Support the management of the Stability Programme, ensuring on-time testing, data review and maintenance of stability records.
• Maintain inventory, proper handling, labelling and disposition of reference standards and control materials, including management after expiry as per SOPs.
• Ensure strict adherence to GMP, GLP and laboratory safety requirements; actively participate in EHS activities, risk assessments and continuous safety improvements.
• Contribute to testing of new products and product development samples, including method verification/validation where required.
• Participate in and deliver mandatory OJT / GMP training; maintain personal training compliance.
• Support preparation, review and revision of SOPs, testing standards and methods to ensure documents remain current and compliant with GMP.
• Use standard computer software and laboratory informatics systems (e.g. LIMS, SAP, instrument software) for data entry, reporting and instrument operation.
• Manage destruction of analysed product materials and hazardous chemical waste in line with EHS and GMP requirements.
• Perform any other tasks assigned by line management in support of business and quality objectives.

Skills

Data Integrity

Detail-Oriented

Digital Fluency

GxP Regulations

Lean Management

Problem Solving

Quality Assurance

Quality Control

Risk Awareness

Testing Operations

Education

Bachelor’s in Applied Chemistry

Chemistry/Industrial Chemistry related discipline

Tools

LIMS

SAP

Instrument Software

Job description

Job Purpose

The Lab Analyst will ensure Quality Compliance of Products / Materials at various stages of testing (including raw material, intermediate and finished product & 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

• Receive and analyse representative samples of finished product, intermediate product, raw materials, stability and trace/CLV to enable timely release by Lab Operations.

• Perform routine and non-routine testing, including stability and validation samples, interpret results and escalation OOS/OOT in line with GMP and site procedures.

• Support the management of the Stability Programme, ensuring on-time testing, data review and maintenance of stability records.

• Maintain inventory, proper handling, labelling and disposition of reference standards and control materials, including management after expiry as per SOPs.

• Ensure strict adherence to GMP, GLP and laboratory safety requirements; actively participate in EHS activities, risk assessments and continuous safety improvements.

• Contribute to testing of new products and product development samples, including method verification/validation where required.

• Participate in and deliver mandatory OJT / GMP training; maintain personal training compliance.

• Support preparation, review and revision of SOPs, testing standards and methods to ensure documents remain current and compliant with GMP.

• Use standard computer software and laboratory informatics systems (e.g. LIMS, SAP, instrument software) for data entry, reporting and instrument operation.

• Manage destruction of analysed product materials and hazardous chemical waste in line with EHS and GMP requirements.

• Perform any other tasks assigned by line management in support of business and quality objectives.

Education, Experience & Skills

• Minimum bachelor’s in applied chemistry, Chemistry, Industrial Chemistry or a related discipline.

• 1-2 years of Experience in a pharmaceutical QC laboratory or similar regulated environment.

• Fundamental understanding of pharmaceutical quality control, analytical techniques and GMP/GLP principles.

• Hands-on experience with analytical instruments and stability/validation testing.

• Familiarity with EHS requirements for laboratory operations and hazardous waste management.

• Continuous improvement mindset and willingness to contribute to SOP/method updates and quality initiatives.

• Good proficiency in standard computer applications; willingness to learn and use LIMS/SAP and instrument software.

• Effective communication skills and ability to work collaboratively within cross-functional teams.

Skills

Data Integrity, Detail-Oriented, Digital Fluency, GxP Regulations, Lean Management, Problem Solving, Quality Assurance (QA), Quality Control (QC), Risk Awareness, Testing Operations

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 – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’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.