Senior Pharmaceutical Analytical Scientist

Placements24; Mossel Bay; On-site; ZAR 700,000 - 1,200,000; Full time

Benefits offered by this job

Health benefits

Continuous learning

Career growth opportunities

Paid leave

Job summary

Placements24 represents a prominent pharmaceutical company in Mossel Bay seeking a Senior Pharmaceutical Analytical Scientist to lead method development, validation, and stability testing in a cGMP environment.

The role requires 5+ years in pharmaceutical analytics, strong HPLC/GC skills, and familiarity with SAHPRA/FDA regulatory expectations. You will work within a well-equipped lab, collaborating across QA, regulatory, and R&D teams to ensure product quality and compliance.

Qualifications

• Master's or PhD in Analytical Chemistry, Pharmaceutical Sciences, or a related field.
• Minimum of 5 years hands-on experience in pharmaceutical analytical development and quality control.
• Extensive expertise operating and troubleshooting analytical instruments (HPLC, GC).
• Strong understanding of method development and validation per ICH guidelines.
• Experience with stability testing programs and regulatory requirements (SAHPRA, FDA).
• Excellent problem-solving and communication skills.
• Ability to manage multiple projects and prioritize effectively.

Responsibilities

• Develop, validate, and transfer analytical methods for drug substances and finished products.
• Perform routine and non-routine analytical testing using instrumental techniques (HPLC, GC, UV-Vis, IR).
• Conduct stability studies and analyze data to assess shelf-life.
• Analyze raw materials, intermediates, and finished products to meet specs.
• Troubleshoot instrumentation and resolve testing issues.
• Prepare and review validation and stability reports and other docs.
• Ensure laboratory activities comply with cGMP, GLP, and regulatory requirements.
• Collaborate with QA, regulatory affairs, and formulation teams.

Skills

Analytical method development

Regulatory compliance

Problem solving

Communication

Project management

Education

Master's or PhD in Analytical Chemistry or Pharmaceutical Sciences

Tools

HPLC

GC

UV-Vis

IR

Job description

About the Role

Our client, a prominent pharmaceutical company based in Mossel Bay, Western Cape , is seeking to hire a Senior Pharmaceutical Analytical Scientist. This role is critical for ensuring the quality and compliance of pharmaceutical products through rigorous analytical testing and method development. The successful candidate will be responsible for overseeing a range of analytical activities, including method validation, stability testing, and raw material analysis, adhering strictly to regulatory guidelines. You will work within a well-equipped laboratory environment, collaborating with cross‑functional teams to support product development and release. This is an excellent opportunity for an experienced analytical chemist to advance their career in the pharmaceutical industry in the picturesque setting of Mossel Bay .

Key Responsibilities

• Develop, validate, and transfer analytical methods for drug substances and finished products according to ICH guidelines.
• Perform routine and non‑routine analytical testing using various instrumental techniques (e.g., HPLC, GC, UV‑Vis, IR, KF).
• Conduct and manage stability studies, analyzing samples and interpreting data to assess product shelf‑life.
• Analyze raw materials, intermediates, and finished products to ensure they meet predefined specifications.
• Troubleshoot analytical instrumentation and resolve analytical issues encountered during testing.
• Prepare and review analytical method validation reports, stability reports, and other technical documentation.
• Ensure all laboratory activities comply with cGMP, GLP, and relevant regulatory requirements.
• Collaborate with formulation scientists, quality control, and regulatory affairs teams.
• Maintain laboratory equipment and ensure compliance with calibration and maintenance schedules.
• Stay updated on industry trends and advancements in pharmaceutical analytical sciences.

Requirements

• Master's or PhD degree in Analytical Chemistry, Pharmaceutical Sciences, or a related field.
• Minimum of 5 years of hands‑on experience in pharmaceutical analytical development and quality control.
• Extensive expertise in operating and troubleshooting analytical instruments, particularly HPLC and GC.
• Strong understanding of analytical method development and validation principles as per ICH guidelines.
• Experience with stability testing programs and data analysis.
• Knowledge of regulatory requirements for pharmaceutical product testing (e.g., SAHPRA, FDA).
• Excellent problem‑solving abilities and attention to detail.
• Strong written and verbal communication skills.
• Ability to manage multiple projects and prioritize effectively.
• Experience working in a pharmaceutical R&D or QC environment in the Western Cape is preferred.

Benefits

• Competitive salary package reflective of experience and expertise.
• Comprehensive health and wellness benefits.
• Opportunities for continuous learning and professional growth.
• Access to advanced analytical instrumentation and technologies.
• A stable and rewarding work environment in Mossel Bay .
• Generous paid leave and holiday allowance.
• Potential for career advancement within the organization.