Validation Engineer (Pharma)

Step into a Career in Pharmaceutical Manufacturing & Quality Looking to build your experience in a structured, regulated manufacturing environment? This opportunity offers hands-on exposure in validation and compliance within a reputable global setup. Why Join This Opportunity: • Monday – Friday, 8:00 AM – 5:00 PM (office hours) • Salary up to 6K (Depending on experienence) • 1-year contract with completion bonus & additional allowances • Comprehensive medical benefits, Company transport provided • Gain valuable experience within a structured and compliance-driven environment What You’ll Be Doing: • Execute validation activities (e.g. equipment, process, or cleaning) in accordance with GMP requirements • Prepare and review validation protocols, reports, and supporting documentation • Investigate deviations and support corrective & preventive actions (CAPA) • Work closely with cross-functional teams to ensure compliance with quality standards • Support continuous improvement initiatives to enhance processes and efficiency What We’re Looking For: • Background in Engineering, Life Sciences, or related field • Prior exposure to GMP or regulated manufacturing environment is an advantage • Detail-oriented with strong documentation and problem-solving skills By submitting your resume, you consent to the collection, use, and disclosure of your personal information per ScienTec’s Privacy Policy (scientecconsulting.com/privacy-policy).  This authorizes us to:  Contact you about potential opportunities.  Delete personal data as it is not required at this application stage.  All applications will be processed with strict confidence. Only shortlisted candidates will be contacted.  Poh Tze Qi (Kayley) | R2197837   ScienTec Consulting Pte Ltd | 11C5781