Pharma QC Analyst: HPLC/GC Testing & Training

Placements24; Queenstown; On-site; NZD 46,000 - 59,000; Full time

Benefits offered by this job

Medical aid benefits

Provident fund participation

On-the-job training and development

Annual leave and sick leave

Job summary

Placements24 is seeking a Quality Control Analyst for our pharmaceutical client in Queenstown (Eastern Cape). You will perform routine analytical testing of raw materials, in-process samples and finished products using HPLC, GC and UV-Vis spectroscopy, ensuring GMP compliance and high data integrity.

You will calibrate instruments, review results, and participate in method validation and OOS investigations while maintaining meticulous records and a safe lab environment.

Qualifications

• Bachelor's degree in Chemistry, Pharmacy, Biotechnology, or related field.
• Minimum 2 years of Quality Control lab experience.
• Proficiency with HPLC, GC, UV-Vis and wet chemistry.
• GMP familiarity and regulatory knowledge.
• Experience with LIMS desirable.

Responsibilities

• Perform routine analytical testing of raw materials, intermediates and finished products using HPLC, GC, UV-Vis and titrations.
• Conduct stability testing and environmental monitoring per protocols.
• Prepare reagents, standards and solutions for analyses.
• Calibrate and maintain laboratory equipment and track calibration schedules.
• Document all activities and results in GMP-compliant systems.
• Investigate OOS results and assist with root cause analysis.
• Assist in validation/verification of methods and equipment.
• Review data to ensure products meet specifications.
• Maintain a clean, organized and safe laboratory.
• Comply with health, safety and environmental regulations.

Skills

HPLC

GC

UV-Vis spectroscopy

Wet chemistry

Data accuracy

Independent & team work

Education

Bachelor's degree in Chemistry, Pharmacy, Biotechnology, or related

Tools

LIMS

Job description

Placements24 is seeking a Quality Control Analyst for our pharmaceutical client in Queenstown (Eastern Cape). You will perform routine analytical testing of raw materials, in-process samples and finished products using HPLC, GC and UV-Vis spectroscopy, ensuring GMP compliance and high data integrity.

You will calibrate instruments, review results, and participate in method validation and OOS investigations while maintaining meticulous records and a safe lab environment.