Senior Analytical Chemist — GMP QC Method Expert

Placements24

Queenstown

On-site

NZD 96,000 - 138,000

Full time

2 days ago
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Benefits offered by this job

Medical aid
Retirement fund
Performance incentives
Modern laboratory facilities
Professional development

Job summary

Placements24 invites applications for a Senior Analytical Chemist in Queenstown. The role focuses on developing, validating, and implementing analytical methods for raw materials, in-process samples, and finished products within the Quality Control and Assurance department.

The ideal candidate will have a Master’s in Analytical Chemistry and 6+ years of pharma experience, with hands-on HPLC/GC expertise, GMP knowledge, and strong data analysis skills.

Qualifications

  • Master's degree in Analytical Chemistry or a related discipline.
  • 6+ years of analytical chemistry experience in the pharmaceutical industry.
  • Experience with HPLC and GC including method development and validation.
  • Solid understanding of GMP and regulatory guidelines.
  • Strong data analysis and interpretation skills.
  • Excellent written and verbal communication.

Responsibilities

  • Develop, validate, and transfer analytical methods for APIs, intermediates, and finished products.
  • Perform routine and non-routine analytical testing using HPLC, GC, UV-Vis, FTIR, KF titration, and dissolution testing.
  • Prepare comprehensive reports for QA and regulatory submissions.
  • Troubleshoot instrumentation and methods and implement corrective actions.
  • Maintain calibration and qualification of laboratory equipment; train junior staff.

Skills

HPLC
GC
UV-Vis
FTIR
Data analysis

Education

Master's degree in Analytical Chemistry or related

Tools

HPLC systems
GC systems
FTIR spectrometer
Dissolution tester
KF titrator

Job description

Placements24 invites applications for a Senior Analytical Chemist in Queenstown. The role focuses on developing, validating, and implementing analytical methods for raw materials, in-process samples, and finished products within the Quality Control and Assurance department.

The ideal candidate will have a Master’s in Analytical Chemistry and 6+ years of pharma experience, with hands-on HPLC/GC expertise, GMP knowledge, and strong data analysis skills.

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