Senior Pharmaceutical Quality Control Analyst

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

Benefits offered by this job

Competitive salary

Medical aid

Provident Fund

Professional development opportunities

Generous annual leave

Paid sick leave

Wellness initiatives

Job summary

Placements24 is seeking a Senior Pharmaceutical Quality Control Analyst for our Queenstown facility. The role focuses on analytical testing of raw materials, in-process samples, and finished products, with responsibility for method validation, data integrity, and regulatory compliance.

The ideal candidate holds a chemistry degree (BSc or MSc) and at least 5 years of QC experience, with hands-on use of HPLC, GC, UV-Vis, FTIR, Karl Fischer, and dissolution equipment.

Qualifications

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Chemistry, or a related field.
• Minimum 5 years of hands-on QC Analyst experience in pharmaceutical industry.
• Proficiency with analytical instruments: HPLC, GC, UV-Vis, FTIR, Karl Fischer, dissolution testers.

Responsibilities

• Perform a wide range of analytical tests on materials and finished products.
• Operate, calibrate, and maintain analytical instrumentation (HPLC, GC, UV-Vis, FTIR, dissolution testers).
• Develop and validate analytical methods per ICH guidelines; transfer methods.
• Analyze data, prepare certificates of analysis and reports; investigate OOS and deviations.
• Assist in audits and maintain cGMP/GLP compliance.

Skills

Analytical chemistry

Data analysis

Attention to detail

Written & verbal communication

Independent work

Education

Bachelor's degree in Chemistry/Pharmaceutical Chemistry

Master's degree preferred

Tools

HPLC

GC

UV-Vis

FTIR

Karl Fischer titrator

Dissolution testers

Job description

About the Role

Our client, a renowned pharmaceutical manufacturer, is seeking a highly skilled and experienced Senior Pharmaceutical Quality Control Analyst to join their laboratory team in Queenstown, Eastern Cape . This role is pivotal in ensuring the quality and integrity of our pharmaceutical products by performing a comprehensive range of analytical tests. You will be responsible for executing tests on raw materials, intermediates, and finished products, validating analytical methods, and maintaining laboratory compliance with cGMP and regulatory standards. The ideal candidate will possess a strong background in analytical chemistry, extensive experience with various analytical instruments, and a meticulous approach to data analysis and reporting. This is a fantastic opportunity to contribute to patient safety and product excellence in a challenging yet rewarding environment. This is a No remote position, requiring full-time dedication at our Queenstown facility.

Key Responsibilities

Perform a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using various instrumental and wet chemistry techniques. Operate, maintain, and calibrate analytical instrumentation, including HPLC, GC, UV-Vis spectrophotometers, FTIR, and dissolution apparatus. Develop, validate, and transfer analytical methods in accordance with pharmacopoeial and regulatory requirements. Analyze and interpret test data, ensuring accuracy and compliance with specifications. Prepare accurate and timely analytical reports, certificates of analysis, and other required documentation. Investigate out-of-specification (OOS) results, deviations, and laboratory investigations, implementing corrective actions. Ensure all laboratory activities are performed in compliance with cGMP, GLP, and relevant regulatory guidelines. Assist in the training and mentoring of junior QC analysts. Contribute to laboratory safety programs and ensure proper handling of chemicals and samples. Participate in internal and external audits as required.

Requirements

Bachelor's degree or Master's degree in Chemistry, Pharmaceutical Chemistry, or a related scientific field. A minimum of 5 years of hands-on experience as a QC Analyst in the pharmaceutical industry. Proficiency in operating and maintaining analytical instruments such as HPLC, GC, UV-Vis, FTIR, Karl Fischer titrator, and dissolution testers. Experience with method development and validation according to ICH guidelines. Thorough understanding of cGMP, GLP, and pharmacopoeial standards (USP, EP, BP). Strong analytical and problem-solving skills, with exceptional attention to detail. Excellent written and verbal communication skills, with the ability to document results clearly and accurately. Ability to work independently and manage multiple priorities effectively. Experience with stability testing programs is a plus. Commitment to maintaining a safe and compliant laboratory environment.

Benefits

Our client offers a competitive salary that reflects your skills and experience, along with potential performance-based bonuses. Comprehensive medical aid coverage and a Provident Fund are provided for your well-being and future security. Opportunities for professional development are abundant, including access to advanced training courses, workshops, and support for relevant scientific certifications. The laboratory environment in Queenstown, Eastern Cape is well-equipped and supportive. Additional benefits include generous annual leave, paid sick leave, and employee wellness initiatives. This is a crucial full-time role within our quality control department.