Senior Quality Control Analyst - Pharmaceutical Testing

Placements24; Mbombela (Nelspruit); On-site; ZAR 420,000 - 660,000; Full time

Benefits offered by this job

Competitive salary

Bonuses

Medical coverage

Retirement plan

Paid time off

Holidays

Professional development

Wellness programs

Job summary

Placements24 is partnering with a reputable pharmaceutical manufacturer to appoint a Senior Quality Control Analyst for their Nelspruit laboratory. The role involves performing a wide range of analytical tests on raw materials, in-process samples, and finished products to ensure products meet GMP, regulatory, and quality standards, safeguarding patient safety.

The successful candidate will calibrate and maintain analytical instruments (HPLC, GC, UV-Vis), document results, investigate OOS

Qualifications

• Bachelor's degree in Chemistry, Biochemistry, Pharmacy, or related field.
• Minimum of 4 years of experience in a pharmaceutical QC laboratory.
• Proficiency with analytical instrumentation such as HPLC, GC, spectrophotometry, and wet chemistry.
• Strong GMP/GMP knowledge and regulatory understanding.
• Experience with pharmacopeial methods (USP, EP, BP).
• Excellent attention to detail and data recording.
• Able to work independently and as part of a team.

Responsibilities

• Perform analytical tests on raw materials, intermediates, and finished pharmaceutical products using techniques (HPLC, GC, UV-Vis, KF).
• Analyze test results for accuracy and compliance with specifications.
• Prepare and standardize reagents and solutions for testing.
• Operate, calibrate, and maintain laboratory equipment per SOPs.
• Document all testing activities in notebooks and LIMS.
• Investigate OOS results and identify root causes.
• Participate in method validation and transfer activities.
• Ensure GLP and GMP compliance.
• Train junior analysts on procedures and techniques.
• Contribute to QC process improvements.

Skills

Analytical thinking

Attention to detail

Problem-solving

Team collaboration

Written and verbal communication

Education

Bachelor's degree in Chemistry, Biochemistry, Pharmacy or related field

Tools

HPLC

GC

Spectrophotometry

KF titration

LIMS

Job description

About the Role

Our client, a reputable pharmaceutical manufacturer committed to producing high-quality medicines, is seeking a meticulous and experienced Senior Quality Control Analyst for their laboratory in Nelspruit. This essential role involves performing a wide range of analytical tests on raw materials, in-process samples, and finished products to ensure they meet stringent quality standards and regulatory requirements. The Senior Quality Control Analyst will play a key part in maintaining product integrity and patient safety through precise and reliable testing. This is an excellent opportunity for a detail-oriented scientist to advance their career within a dynamic quality control environment. The ideal candidate will possess strong analytical skills and a thorough understanding of pharmaceutical testing methodologies. We foster a culture of quality excellence and provide opportunities for professional growth within our Nelspruit facility. The Nelspruit location provides a supportive environment for a career focused on ensuring the highest standards of pharmaceutical quality.

Key Responsibilities

• Perform analytical tests on raw materials, intermediates, and finished pharmaceutical products using various techniques (e.g., HPLC, GC, UV-Vis, KF titration).
• Analyze test results for accuracy, completeness, and compliance with established specifications.
• Prepare and standardize reagents and solutions for analytical testing.
• Operate, calibrate, and maintain laboratory equipment according to SOPs and manufacturer guidelines.
• Document all testing activities, results, and observations accurately and meticulously in laboratory notebooks and LIMS.
• Investigate out-of-specification (OOS) results, identify root causes, and implement corrective actions.
• Participate in method validation and transfer activities.
• Ensure compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Train junior analysts on laboratory procedures and analytical techniques.
• Contribute to the continuous improvement of QC processes and procedures.

Requirements

• Bachelor's degree in Chemistry, Biochemistry, Pharmacy, or a related scientific discipline.
• Minimum of 4 years of experience in a pharmaceutical Quality Control laboratory setting.
• Proven proficiency with analytical instrumentation such as HPLC, GC, spectrophotometry, and wet chemistry techniques.
• Solid understanding of pharmaceutical quality control principles, GMP, and regulatory requirements.
• Experience with pharmacopeial methods (e.g., USP, EP, BP).
• Strong analytical, problem-solving, and critical thinking skills.
• Excellent attention to detail and accuracy in data recording and reporting.
• Effective written and verbal communication skills.
• Ability to work independently and as part of a team in a fast-paced environment.
• Familiarity with laboratory information management systems (LIMS) is advantageous.

Benefits

• Our client offers a competitive salary, potential for annual bonuses, and a comprehensive benefits package including medical, dental, and vision coverage.
• We provide a retirement savings plan, generous paid time off, and company-paid holidays.
• Opportunities for professional development and training in new analytical techniques are available.
• The Nelspruit laboratory is well-equipped and provides a collaborative atmosphere.
• Employees also benefit from wellness programs and employee assistance services.

This role in Nelspruit is crucial for ensuring the quality and safety of pharmaceutical products. Join our dedicated team and contribute to public health.