Senior Analytical Scientist

Placements24; Riverton (UT); On-site; USD 54,000 - 85,000; Full time

Benefits offered by this job

Competitive salary

Medical, dental, and vision insurance

Retirement savings plan

Paid time off and holidays

Professional development and training

Relocation assistance

Job summary

Placements24 is seeking a Senior Analytical Scientist for our client in Upington, South Africa, to lead analytical development in the Quality Control and Assurance department.

The role requires 5+ years in pharma analytics, with hands-on HPLC/GC/MS experience, and a strong grasp of regulatory guidelines. You will mentor staff, drive method validation, and contribute to audits and process improvements.

Qualifications

• M.Sc. or Ph.D. in Analytical Chemistry, Organic Chemistry, Pharmaceutical Sciences, or a related field.
• Minimum of 5 years of experience in analytical development and quality control within the pharmaceutical industry.
• Extensive hands‑on experience with HPLC, GC, Mass Spectrometry, and other relevant analytical techniques.
• Strong understanding of method validation principles and ICH guidelines.
• Proven ability to develop, troubleshoot, and optimize analytical methods.
• Proficiency in data analysis and interpretation using relevant software (e.g., Empower, ChemStation).
• Excellent knowledge of GMP and regulatory compliance requirements.
• Strong problem-solving skills and attention to detail.
• Effective written and verbal communication skills.
• Ability to work independently and as part of a collaborative team.
• Experience in leading analytical projects is a significant advantage.

Responsibilities

• Develop, validate, and implement analytical methods for raw materials, in-process samples, and finished pharmaceutical products using techniques such as HPLC, GC, MS, UV-Vis, FTIR, and dissolution testing.
• Perform routine and non-routine analytical testing according to established SOPs and regulatory guidelines.
• Troubleshoot and resolve analytical issues encountered during method development, validation, or routine testing.
• Conduct stability studies and analyze data to determine product shelf-life and storage conditions.
• Interpret complex analytical data and generate comprehensive reports.
• Ensure compliance with GMP, GLP, and other regulatory requirements.
• Maintain laboratory equipment, including calibration, qualification, and preventive maintenance.
• Mentor and provide technical guidance to junior analytical chemists and technicians.
• Participate in internal and external audits as an analytical SME.
• Contribute to continuous improvement of analytical processes and methodologies.
• Stay updated with the latest advancements in analytical chemistry and pharmaceutical regulations.

Skills

Analytical development

Quality control experience

Data analysis

Leadership experience

Problem-solving

Education

M.Sc. or Ph.D. in Analytical Chemistry or related field

Tools

HPLC

GC

Mass Spectrometry

Empower

ChemStation

Job description

About the Role Our client, a leading pharmaceutical research and manufacturing company, is seeking a highly skilled Senior Analytical Scientist to join their Quality Control and Assurance department in Upington, Northern Cape.

Key Responsibilities

• Develop, validate, and implement analytical methods for raw materials, in-process samples, and finished pharmaceutical products using techniques such as HPLC, GC, MS, UV-Vis, FTIR, and dissolution testing.
• Perform routine and non-routine analytical testing according to established SOPs and regulatory guidelines.
• Troubleshoot and resolve analytical issues encountered during method development, validation, or routine testing.
• Conduct stability studies and analyze data to determine product shelf-life and storage conditions.
• Interpret complex analytical data and generate comprehensive reports.
• Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory requirements.
• Maintain laboratory equipment, including calibration, qualification, and preventative maintenance.
• Mentor and provide technical guidance to junior analytical chemists and technicians.
• Participate in internal and external audits as an analytical subject matter expert.
• Contribute to the continuous improvement of analytical processes and methodologies.
• Stay updated with the latest advancements in analytical chemistry and pharmaceutical regulations.

Requirements

• M.Sc. or Ph.D. in Analytical Chemistry, Organic Chemistry, Pharmaceutical Sciences, or a related field.
• Minimum of 5 years of experience in analytical development and quality control within the pharmaceutical industry.
• Extensive hands‑on experience with HPLC, GC, Mass Spectrometry, and other relevant analytical techniques.
• Strong understanding of method validation principles and ICH guidelines.
• Proven ability to develop, troubleshoot, and optimize analytical methods.
• Proficiency in data analysis and interpretation using relevant software (e.g., Empower, ChemStation).
• Excellent knowledge of GMP and regulatory compliance requirements.
• Strong problem-solving skills and attention to detail.
• Effective written and verbal communication skills.
• Ability to work independently and as part of a collaborative team.
• Experience in leading analytical projects is a significant advantage.

Benefits

• Competitive salary and bonus structure.
• Comprehensive medical, dental, and vision insurance.
• Retirement savings plan with company contributions.
• Generous paid time off and company holidays.
• Opportunities for professional development, including specialized training and conference attendance.
• Access to modern analytical instrumentation and facilities in Upington.
• A supportive and quality-focused work environment.
• Potential for career advancement within the organization.
• Relocation assistance may be available.