GMP Trainee: Pharma Ops & Compliance (15-Month Program)

Lonza Group Ltd.

Singapore

Vor Ort

SGD 27.000 - 36.000

Vollzeit

14 Tage+
Bewerbungsgenerator

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Benefits dieser Stelle

Agile career culture
Inclusive workplace
Daily bus from MRT to Tuas site

Zusammenfassung

Lonza Group Ltd. in Singapore Tuas is offering a 15-month site-based trainee program within a GMP-regulated manufacturing environment. You will learn and apply GMP principles, SOPs, and company policies while supporting day-to-day operations and documentation under supervision.

The role involves basic laboratory and technical tasks, equipment monitoring, and collaboration with cross-functional teams. A diploma/degree in a relevant science field is required, with strong communication and

Qualifikationen

  • Diploma/ Degree in relevant science discipline.
  • Strong interpersonal and communication skills.
  • Meticulous attention to detail and teamwork.
  • Willingness to learn GMP and regulatory requirements.

Aufgaben

  • Learn and apply GMP principles, SOPs, and company policies in daily activities.
  • Support routine operations within assigned departments while maintaining compliance with quality, safety, and regulatory requirements.
  • Assist with documentation, data entry, record review, and maintenance of GMP documents (logbooks, batch records, reports).
  • Perform basic laboratory, manufacturing, or technical tasks under supervision.
  • Support equipment monitoring, housekeeping, and workplace organization.
  • Participate in sample collection, testing, investigations, or process monitoring activities where applicable.
  • Assist with equipment qualification, validation, technology transfer, or process improvement initiatives.

Kenntnisse

Interpersonal skills
Verbal and written communication
Detail oriented
Team player

Ausbildung

Diploma/ Degree in relevant science discipline

Tools

LIMS
MES
ERP

Jobbeschreibung

Lonza Group Ltd. in Singapore Tuas is offering a 15-month site-based trainee program within a GMP-regulated manufacturing environment. You will learn and apply GMP principles, SOPs, and company policies while supporting day-to-day operations and documentation under supervision.

The role involves basic laboratory and technical tasks, equipment monitoring, and collaboration with cross-functional teams. A diploma/degree in a relevant science field is required, with strong communication and

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