Senior Analytical Chemist - Pharmaceutical

Placements24; Queenstown; On-site; NZD 96,000 - 138,000; Full time

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

About the Role

Our client, a prominent pharmaceutical company dedicated to developing high-quality therapeutic products, is seeking a Senior Analytical Chemist to join their Quality Control and Assurance department in Queenstown, Eastern Cape . This vital role focuses on developing, validating, and implementing analytical methods for raw materials, in-process samples, and finished products. You will play a key role in ensuring product quality and compliance with regulatory standards through rigorous testing and data analysis. The ideal candidate will possess extensive experience with a variety of analytical techniques, a strong understanding of pharmaceutical regulations, and a meticulous approach to quality control. This position offers a challenging and rewarding career within a company committed to scientific excellence and patient well-being.

Key Responsibilities

Develop, validate, and transfer analytical methods for pharmaceutical raw materials, intermediates, and finished products according to ICH guidelines. Perform routine and non-routine analytical testing using techniques such as HPLC, GC, UV-Vis, FTIR, KF titration, and dissolution testing. Analyze and interpret analytical data, preparing comprehensive reports for quality assurance and regulatory submissions. Troubleshoot analytical instrumentation and methods, identifying root causes of issues and implementing corrective actions. Maintain laboratory equipment and ensure its calibration and qualification. Collaborate with R&D, production, and regulatory affairs teams to support product development and manufacturing. Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulatory requirements. Train and mentor junior analytical chemists and technicians. Contribute to process improvement initiatives within the QC laboratory. Stay updated on current analytical technologies and regulatory trends in the pharmaceutical industry.

Requirements

Master's degree in Analytical Chemistry, Pharmaceutical Chemistry, or a related discipline. A minimum of 6 years of experience in analytical chemistry within the pharmaceutical industry. Extensive hands-on experience with HPLC and GC systems, including method development and validation. Proficiency in operating and maintaining various analytical instruments. Solid understanding of pharmaceutical quality control, GMP, and regulatory guidelines. Strong data analysis and interpretation skills. Excellent problem-solving abilities and attention to detail. Effective written and verbal communication skills. Ability to manage multiple tasks and prioritize effectively in a busy laboratory environment. Experience with stability studies and method transfer is desirable.

Benefits

Our client offers a competitive salary, a comprehensive benefits package including medical aid, retirement fund, and performance incentives. Employees have access to modern laboratory facilities and opportunities for professional development and training. The work environment in Queenstown, Eastern Cape is professional and team-oriented, supporting a healthy work-life balance. This role provides an excellent opportunity to contribute to the delivery of safe and effective medicines.