Quality Control Analyst - Full-time

Placements24; East London; Presencial; ZAR 360.000 - 600.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical aid

Retirement fund

Paid annual leave

Professional development

Descripción de la vacante

Placements24 seeks a Quality Control Analyst for a pharmaceutical manufacturing company in East London, SA. You will perform analytical testing on raw materials, in-process samples, and finished products, ensuring compliance with GMP/GLP and regulatory standards.

Responsibilities include method validation participation, equipment calibration, and precise data reporting; a Bachelor’s in Chemistry/Pharmacy and 2+ years QC lab experience are required.

Formación

• Bachelor's degree in Chemistry, Pharmacy, or related discipline.
• 2+ years in a pharmaceutical QC lab environment.
• Proficiency with analytical instruments: HPLC and GC.
• Knowledge of GMP and GLP principles.
• Strong data recording and reporting accuracy.
• Proficient in Microsoft Office tools.

Responsabilidades

• Perform analytical testing of raw materials, intermediates and finished products using HPLC, GC, UV-Vis and titration.
• Prepare reagents, solutions, and standards for testing.
• Record, document, and report test results per GLP and SOPs.
• Calibrate and maintain lab equipment to ensure accuracy.
• Troubleshoot analytical methods and equipment; escalate issues as needed.
• Participate in method validation and transfer activities.

Conocimientos

Attention to detail

Communication

Organizational skills

Teamwork

Educación

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

Herramientas

HPLC

GC

UV-Vis

Titration

Microsoft Office Suite

Descripción del empleo

About the Role

Our client, a leading pharmaceutical manufacturing company, is looking for a dedicated Quality Control Analyst to join their laboratory team in East London, Eastern Cape, ZA. This role is integral to ensuring the consistent quality and safety of our client's pharmaceutical products through rigorous testing and analysis. As a QC Analyst, you will perform a variety of laboratory tests on raw materials, in-process samples, and finished products, ensuring they meet stringent specifications and regulatory standards. This is an excellent opportunity for a scientifically inclined individual to contribute to high-quality pharmaceutical production and develop their career in quality control.

Key Responsibilities

• Perform analytical testing of raw materials, intermediates, and finished products using various laboratory techniques (e.g., HPLC, GC, UV-Vis, titration).
• Prepare reagents, solutions, and standards required for testing.
• Accurately record, document, and report test results according to established procedures and Good Laboratory Practices (GLP).
• Calibrate and maintain laboratory equipment, ensuring its proper functioning and accuracy.
• Troubleshoot analytical methods and equipment issues, escalating as necessary.
• Participate in method validation and transfer activities.
• Ensure adherence to all safety procedures and maintain a clean and organized laboratory environment.
• Review batch records and analytical data for completeness and accuracy.
• Contribute to the continuous improvement of laboratory processes and quality systems.

Requirements

• Bachelor's degree in Chemistry, Pharmacy, or a related scientific discipline.
• A minimum of 2 years of experience in a pharmaceutical Quality Control laboratory setting.
• Proficiency in operating and maintaining analytical laboratory instrumentation, particularly HPLC and GC.
• Solid understanding of analytical chemistry principles and techniques.
• Familiarity with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
• Strong attention to detail and accuracy in data recording and reporting.
• Excellent organizational skills and the ability to manage multiple tasks effectively.
• Proficiency in Microsoft Office Suite.
• Strong written and verbal communication skills.
• Must be able to work effectively in a laboratory setting in East London, Eastern Cape, ZA.

Benefits

• Our client offers a competitive salary, commensurate with experience and qualifications.
• The benefits package includes medical aid, a retirement fund, and paid annual leave.
• Opportunities for professional development and training in advanced analytical techniques will be provided.
• You will be working in a modern laboratory facility with state-of-the-art equipment.
• Join a supportive and professional team dedicated to ensuring the quality and safety of pharmaceutical products manufactured in East London, Eastern Cape, ZA.
• This is a stable role within a well-established company.