About this role
The role will focus on supporting training development, laboratory operations, documentation activities, and quality processes to ensure compliance with internal and regulatory requirements. Jobscope: • Support the development and maintenance of Quality training materials and competency-based learning packages. • Work with Subject Matter Experts (SMEs) and cross-functional teams to gather information and support training initiatives. • Assist in creating training content such as learning materials, job aids, and assessments. • Support Operations and Microbiology laboratory activities, including backlog clearance activities. • Assist with drafting, reviewing, and maintaining quality documentation such as SOPs and related records. • Support review activities for QC testing, utilities, and environmental monitoring samples. • Ensure compliance with GMP requirements, company procedures, and quality standards. • Support continuous improvement and day-to-day quality operations activities. Requirements: • • Diploma or Degree in Life Sciences, Chemistry, Biotechnology, Pharmaceutical Sciences, or related disciplines. • Experience in pharmaceutical, biologics, biotechnology, or GMP-regulated manufacturing environments preferred. • Exposure to Quality, QC, QA, laboratory, or manufacturing operations environments is advantageous. • Familiarity with laboratory systems such as Empower or chromatography systems is a plus. • Knowledge of GMP practices and quality documentation processes preferred. • Good communication and stakeholder management skills with strong attention to detail. To find out more about this opportunity, please contact Fiona Koh; fiona.koh@gmprecruit.com We regret that only shortlisted candidates will be notified. GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Fiona Koh | Registration No: R1109239
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