Specialist, Qa Operations (master Batch Record)

Lonza Group

Tuas, Singapore
Competitive compensation programs; comprehensive m...
Not specified (assumed onsite)
Review batch records and logbooks
Manage deviation investigations with rca
Monitor capa implementation and closure
Lonza Group is seeking a QA Operations Specialist for their Tuas, Singapore facility, focusing on quality assurance activities in a large-scale GMP Biotech Manufacturing environment. The ideal candidate will possess a degree and 2-5 years of relevant experience, with strong communication skills and meticulous attention to detail

Job Summary

  • The role involves providing day-to-day Quality Assurance activities support for a large-scale GMP Biotech Manufacturing facility.
  • Candidates will review batch records, compile lot genealogy, and oversee product status and shipping documentation.
  • Lonza offers competitive compensation, comprehensive medical insurance, company transport, and opportunities for global exposure.

Matching Summary

Match Score: 85

Lonza Group is seeking a QA Operations Specialist for their Tuas, Singapore facility, focusing on quality assurance activities in a large-scale GMP Biotech Manufacturing environment. The ideal candidate will possess a degree and 2-5 years of relevant experience, with strong communication skills and meticulous attention to detail.

Salary

Competitive compensation programs; Comprehensive medical insurance; Company transport provided

Skills & Requirements

Must-have

  • Review batch records and logbooks
  • Manage deviation investigations with RCA
  • Monitor CAPA implementation and closure
  • Conduct shop floor QA walk-downs
  • Support regulatory inspections and audits

Nice-to-have

  • Agile career and dynamic working culture
  • Strong focus on safety and timelines
  • Meticulous and systematic approach
  • Team player with good communication skills
  • Experience in cross-functional projects

Key Requirements

  • Degree with 2-5 years of experience
  • Familiarity with FDA, EMEA, and ICHQ7 regulations
  • Practical knowledge of quality management systems in GMP facilities

Work Rights

Not specified

Tailored Resume

Cover Letter