Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

This role will be responsible for method transfer/verification/validation, and project work supporting the manufacture and release of pharmaceutical raw materials, intermediates, and products. The role contributes to building and maintaining QC lab cGMP systems, delivering analytical solutions to clients through expertise in method qualification and validation strategies, ensuring timely delivery of projects.

Responsibilities:

Support new equipment qualification, lab computerized systems, and chemistry lab setupPerform transfer/verification/validation of laboratory procedures within the teamPrepare technical documentation (protocols, analytical write-ups, SOPs, specifications, reports)Conduct cGMP-compliant analysis of incoming goods, intermediates, and finished productsReview analytical and laboratory data for accuracy, completeness, and procedural complianceStay updated with new pharmacopoeia and regulations; identify and close compliance gapsPerform investigation write-ups and deviations, ensuring timely closure under QMS proceduresManage QC chemical, reference standards, and consumable stock levelsMaintain personal training records and assist in training team membersCommunicate effectively locally and internationally and engage in problem solvingParticipate in Practical Process Improvement (PPI) and continuous improvement initiativesPromote a Quality Culture and the company’s 4i valuesEnsure compliance with cGMP, HSE, and 5S in all areas of workUndertake ad-hoc activities as required by the business

Minimum Requirements / Qualifications:

Degree in Chemistry or closely related scientific disciplineAt least 3 years relevant industry experienceKnowledge and application of GMP regulations and international guidelinesAbility to work independently and meet critical timelinesEffective communication skills at all levelsExcellent attention to detailExcellent organisational skills