GMP/GLP QC Lab Analyst Internship

Pintern

Karachi Division

On-site

PKR 670,000 - 1,004,000

Full time

14 days+

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Job summary

GSK is seeking a Lab Analyst to ensure quality compliance across materials and products through GMP/GLP-aligned testing. You will handle samples, perform analyses, review stability data and support EHS compliance in a regulated laboratory.

The role requires a bachelor’s in chemistry-related field and 1–2 years in a pharmaceutical QC lab, with hands-on instrument experience and willingness to contribute to SOP updates and quality initiatives. Collaborative cross-functional work is essential.

Qualifications

  • Bachelor's degree in applied chemistry, chemistry, industrial chemistry or 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.

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

Tools

LIMS
SAP
Instrument Software

Job description

GSK is seeking a Lab Analyst to ensure quality compliance across materials and products through GMP/GLP-aligned testing. You will handle samples, perform analyses, review stability data and support EHS compliance in a regulated laboratory.

The role requires a bachelor’s in chemistry-related field and 1–2 years in a pharmaceutical QC lab, with hands-on instrument experience and willingness to contribute to SOP updates and quality initiatives. Collaborative cross-functional work is essential.

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