jobs in NOVARTIS SINGAPORE PHARMACEUTICAL MANUFACTURING PTE. LTD.

Kerja Manufacturing Biotechnologist (Career Conversion Programme Trainee), Gaji tinggi SGD 2,560 di NOVARTIS SINGAPORE PHARMACEUTICAL MANUFACTURING PTE. LTD. West Region (Singapore) - Maukerja

Manufacturing Biotechnologist (Career Conversion Programme Trainee)

NOVARTIS SINGAPORE PHARMACEUTICAL MANUFACTURING PTE. LTD.

West Region (Singapore)

Kongsi
Simpan

Lokasi Kerja

  • 8 TUAS BAY LANE West Region (Singapore) Singapore

Penerangan Kerja

Tanggungjawab

Overview of Career Conversion Program (CCP)

Administered by the Workforce Advancement Federation (WAF),the Career Conversion Program (CCP) for Biomedical ManufacturingExecutives/Professional (Attach-And-Train) is a premier talent developmentinitiative designed to cultivate the next generation of skilled professionalsfor Singapore’s Biomedical manufacturing industry. This comprehensive15-monthprogram features structured on-the-job training (OJT) provided atNovartis Singapore Pharmaceutical Manufacturing Pte Ltd (NSPM), facilitatingthe practical application of acquired knowledge and ensuring participantsdevelop the essential competencies required for their roles.

Eligibility for CCP:

  • Singapore Citizen or Permanent Resident, age 21 and above;
  • Mid-Career Individual: Have graduated and/or completed National Service for at least 2 years at the point of application; OR
  • Fresh Graduate: Have graduated and/or completed National Service for less than 2 years at the point of application;
  • Should not be shareholders, ex-employees of Novartis, or be related to shareholders of Novartis.


Job Summary

  • Involve in hands-on execution of the plant operations and trouble-shooting
  • Perform plant setup activities (including cleaning, configuration and equipment dismantling) and carry out “first fix” for plant issues
  • Monitor and analyze processing parameters for atypical trends and improvement opportunities
  • Interface with other departments to resolve issues related to daily operations
  • Write and revise SOPs and other manufacturing related documentations.
  • Support deviations investigations and CAPAs implementations (both Quality and HSE)
  • Support transfer of new processes and commission/validation of new projects
  • Lead / support continuous improvement initiatives
  • Conduct / support GMP and Safety audits


Requirements

  • Diploma in Chemical Engineering, Science or related discipline. ITE graduates open to apply.
  • Able to work on 12-hour rotating shift (morning /night)
  • Able to work in in clean room environment

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