Lab Analyst

Job Purpose
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

• Receiving and analysis of representative samples of Finished product, Intermediate product, Raw material, Stability, Trace/CLV for timely release by Lab operations.
• Release of Finished product, intermediate and Raw material in LIMS & SAP.
• Analysis of Stability or Validation samples and interpretation of results
• Support in the management of Stability Program for timely assure the Stability.
• Inventory Maintenance, handling and disposition of Reference Standards after expiry.
• Follow GMP and safety requirement of Laboratory and participate in Various EHS activities.
• Participate in the testing of new products and product development.
• Conduct and participate in Mandatory OJT/ GMP training sessions.
• Support in preparation and revision of existing SOPS, Testing standards and Testing Methods to set standards as per GMP compliance.
• Demonstrate proficiency in standard computer software for the use of Analytical Instruments.
• Destruction of the product material left after analysis and managing the destruction of hazardous chemical waste.

Education, Experience & Skills

• Bachelor’s or Master’s degree in Pharm D, Applied Chemistry, Chemistry, Biochemistry, Analytical Chemistry, industrial engineering, or a related science discipline.
• 0 to 2 years of relevant laboratory experience in quality control, analytical testing, or a similar regulated environment.
• Practical experience or familiarity with common analytical techniques and instruments such as HPLC, GC, UV-visible spectrophotometry or equivalent.
• Basic computer skills including MS Office and willingness to learn LIMS (Laboratory Information Management System) and SAP or other ERP systems.
• Clear written and verbal communication skills and ability to work collaboratively in diverse teams.
• Understanding of good laboratory and good manufacturing practices and commitment to following procedures.
• Exposure to method validation, method transfer, or finished product testing.
• Experience supporting investigations, root cause analysis and corrective actions.
• Knowledge of quality management systems and document control processes.
• Strong attention to detail, organisation and basic data calculation skills.

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.

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

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