Job description

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