Remote Pharmaceutical Quality Control Analyst

Placements24; Cape Town; Hybride; ZAR 480 000 - 720 000; Plein temps

Avantages offerts par ce poste

Medical aid

Retirement contributions

Performance-based bonuses

Résumé du poste

Placements24 in South Africa is seeking a dedicated Remote Pharmaceutical Quality Control Analyst to support a global leader in pharmaceutical manufacturing. This role focuses on analytical testing, method validation, and data interpretation to ensure products meet regulatory and quality standards.

Ideal candidates have a degree in Chemistry or Pharmaceutical Sciences, at least three years' experience in QC or analytical development, and strong knowledge of ICH cGMP guidelines.

Qualifications

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, Analytical Chemistry, or a related field.
• Minimum of 3 years of experience in pharmaceutical quality control or analytical development.
• Proficiency with analytical instrumentation such as HPLC, GC, UV-Vis, FTIR, and dissolution apparatus.
• Strong knowledge of cGMP, ICH guidelines, and regulatory requirements for pharmaceutical testing.
• Excellent data analysis and interpretation skills, with a proven ability to identify and resolve technical issues.
• Exceptional organizational and time management skills, with the ability to manage multiple tasks effectively in a remote environment.
• Strong written and verbal communication skills for clear and concise reporting.
• Comfortable working independently and as part of a virtual team, demonstrating proactivity and self-motivation.

Responsabilités

• Perform analytical testing of materials and products using techniques (e.g., HPLC, GC, spectroscopy).
• Develop, validate, and transfer analytical methods per ICH guidelines.
• Interpret test results and document deviations or out-of-spec results.
• Troubleshoot instrumentation and maintain calibration.
• Review and approve QC data in line with procedures and regs.
• Collaborate with manufacturing, R&D, and regulatory affairs to resolve quality issues.
• Maintain understanding of cGMP and regulatory standards.
• Prepare technical reports and summaries for management and regulatory submissions.

Connaissances

Analytical chemistry

Data analysis

Remote work

Time management

Written and verbal communication

Independent worker

Formation

Bachelor's or Master's in Chemistry/Pharmaceutical Sciences

Outils

HPLC

GC

UV-Vis

FTIR

Dissolution apparatus

Description du poste

About the Role

Our client, a globally recognized pharmaceutical company, is actively seeking a dedicated and meticulous Remote Pharmaceutical Quality Control Analyst to join their expanding operations. This fully remote position offers the flexibility to work from anywhere within South Africa, allowing you to contribute to critical quality assurance processes without geographical constraints. You will be responsible for ensuring that our pharmaceutical products meet the highest standards of safety, efficacy, and quality through rigorous testing and analysis. This role is vital to maintaining regulatory compliance and upholding the integrity of our product portfolio. The ideal candidate will possess a strong background in analytical chemistry and a keen eye for detail, coupled with the ability to work independently in a remote setting. Join a forward-thinking organization committed to excellence in pharmaceutical manufacturing and quality assurance.

Key Responsibilities

• Perform analytical testing of raw materials, in-process samples, and finished pharmaceutical products using various techniques (e.g., HPLC, GC, spectroscopy).
• Develop, validate, and transfer analytical methods according to ICH guidelines and regulatory requirements.
• Interpret test results, document findings accurately in laboratory notebooks and reports, and identify any deviations or out-of-specification results.
• Troubleshoot analytical instrumentation and methodologies, ensuring equipment is calibrated and maintained.
• Review and approve quality control data, ensuring compliance with internal procedures and external regulations.
• Collaborate with cross-functional teams, including manufacturing, R&D, and regulatory affairs, to resolve quality-related issues.
• Maintain a thorough understanding of current Good Manufacturing Practices (cGMP) and other relevant regulatory standards.
• Prepare technical reports and summaries for internal management and regulatory submissions as required.

Requirements

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, Analytical Chemistry, or a related field.
• Minimum of 3 years of experience in pharmaceutical quality control or analytical development.
• Proficiency with analytical instrumentation such as HPLC, GC, UV-Vis, FTIR, and dissolution apparatus.
• Strong knowledge of cGMP, ICH guidelines, and regulatory requirements for pharmaceutical testing.
• Excellent data analysis and interpretation skills, with a proven ability to identify and resolve technical issues.
• Exceptional organizational and time management skills, with the ability to manage multiple tasks effectively in a remote environment.
• Strong written and verbal communication skills for clear and concise reporting.
• Comfortable working independently and as part of a virtual team, demonstrating proactivity and self-motivation.

Benefits

• This remote position offers a competitive annual salary, a comprehensive benefits package including medical aid and retirement contributions, potential for performance-based bonuses, and extensive opportunities for professional growth and development within a leading pharmaceutical company.
• You will have the autonomy to manage your workday while contributing to vital global health initiatives.