Analyst

2 weeks ago

Karachi, Sindh, Pakistan GlaxoSmithKline Full time
Site Name: Pakistan - Sindh - Karachi
Posted Date: Mar 26 2025

Job Purpose

The purpose of this position is to ensure that all Standard Operating Procedures (SOPs), specifications, test methods, instruments, and regulatory standards are current and in compliance with corporate and regulatory requirements. This involves the inspection and analysis of raw materials, in-process batches, and finished products through both physical and chemical testing. The role is critical in ensuring that Quality Control methods, instrumentation, and procedures meet current Good Manufacturing Practices, Environmental Health and Safety guidelines, Quality Management System requirements, SOPs, and corporate standards. The position plays a key role in maintaining product quality, safety, and regulatory compliance.

Education, Experience & Skills

  • Pharm-D, MSc in Chemistry, MSc in Biochemistry, or equivalent degree.
  • 1-3 years of experience in a similar pharmaceutical role is preferred.
  • Strong communication and presentation skills.
  • Excellent analytical and problem-solving abilities.
  • Proficient in documentation and report writing.

Key Responsibilities

  • Providing support in raw material and finished product sampling, testing and timely release of required material and product for production as per schedule performing tests according to GSK specification to meet the schedule and to maintain an entry of raw analytical records in logbook, Lot registration and test registration at right time in LIMS and its release in DMERP.
  • Update specifications as per Pharmacopeial updates and to ensure that the SOPs, Internal Factory Specification and analytical Test methods should be current and updated.
  • Testing of buying sample for new supplier/manufacturer development in raw material section.
  • Reporting of OOS/Atypical as per relevant SOP.
  • Maintenance and troubleshooting of relevant laboratory equipment and maintaining the records of reagents, solution and standards.
  • Handling and operations on EMPOWER application.
  • Perform daily checking, cleaning calibration record of instruments and maintaining the record of PPEs.
  • Self-training through e-learning modules and attend training courses and Participate in Level 1 audit.
  • Attending in-house SOP and GMP training and maintaining GMP in lab.
  • Actively participating in departmental projects and team meetings and ensuring implementation of lean lab practices in department.
  • Ensure EHS compliance and attend workshops and training courses.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.

Contact information:

You may apply for this position online by selecting the Apply now button.

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