GSK

biopharma

LabAnalyst

Karachi, Pakistan FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Entry candidates.

The Brief

“Lab Analyst at GSK. Skills: analytical testing, laboratory skills, data reporting, LIMS, SAP. Perform testing of raw materials, intermediates, and finished products as per effective IFS and TM. Generate and maintain raw data sheets (logbooks), calculation sheets, summary sheets, and electronically signed reports in LIMS”

What You'll Achieve.

ensure product quality and safety

Industry & Context.

biopharma
Problems you'll solve

investigations; root cause analysis

Eligibility Requirements

on-site in Pakistan, full-time presence at the laboratory

What They're Looking For.

Must Have

Master's degree in Chemistry, Pharm-D or a related life sciences field (16 years of education), At least 2 years of laboratory experience in quality control, analytical testing, or a similar environment, Practical knowledge of common lab techniques and instruments such as titration, spectrophotometry, HPLC, GC or basic microbiology methods, Prior use of LIMS, SAP or other enterprise systems for sample tracking and reporting, Basic understanding of good manufacturing practices, quality systems and data integrity principles, Experience in investigations, root cause analysis and CAPA processes

Nice to Have

Exposure to continuous improvement approaches such as Lean or Six Sigma

What You'll Do.

Perform testing of raw materials

and finished products as per effective IFS and TM

Generate and maintain raw data sheets (logbooks)

and electronically signed reports in LIMS

Operate analytical instruments and related software

Calibrate analytical balances

Prepare laboratory solutions

Maintain reference samples

Support standardization of materials

Perform testing for cleaning and cross-contamination studies

Report LIRs including OOS

and errors in line with quality procedures

Ensure daily GMP-compliant housekeeping

Manage document inventory and issuance across the department

Coordinate with document owners for document preparation and revisions

Liaise with the documentation SME/record champion at site for timely and compliant document destruction

How You'll Work.

Team & Collaboration

Work closely with laboratory colleagues, production and quality teams; Coordinate with document owners for document preparation and revisions; Liaise with the documentation SME/record champion at site

Communication Scope

clear communication

Full Job Description

**Role Summary** You will support analytical testing activities at our Pakistan laboratory to help ensure product quality and safety. You will work closely with laboratory colleagues, production and quality teams. We value practical laboratory skills, clear communication, and a commitment to continuous learning. This role offers hands-on experience, clear career growth, and the chance to contribute to GSK’s mission of uniting science, technology and talent to get ahead of disease together. **Key Responsibilities** * Perform testing of raw materials, intermediates, and finished products as per effective IFS and TM, including data reporting in LIMS and SAP transactions, and sample disposal after release * Generate and maintain raw data sheets (logbooks), calculation sheets, summary sheets, and electronically signed reports in LIMS * Operate analytical instruments and related software, calibrate analytical balances, and prepare laboratory solutions * Maintain reference samples, support standardization of materials, and perform testing for cleaning and cross-contamination studies * Report LIRs including OOS, atypical results, and errors in line with quality procedures * Actively participate in EHS, fire safety, and learning activities, report EHS incidents/adverse events, and ensure daily GMP-compliant housekeeping * Maintain departmental document lists and repositories as per SOP (VQD-SOP-051700) * Manage document inventory and issuance across the department * Coordinate with document owners for document preparation and revisions (e.g. SOPs, impact assessments) * Liaise with the documentation SME/record champion at site for timely and compliant document destruction **Education, Experience & Skills** * Master’s degree in Chemistry, Pharm-D or a related life sciences field (16 years of education). * At least 2 years of laboratory experience in quality control, analytical testing, or a similar environment. Fresh graduates with practical laboratory experience are welcome t

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