Shift Analyst Midrand

Neoc Group Pty Ltd; Gauteng; On-site; ZAR 400 000 - 550 000; Full time

Job summary

A leading company in the pharmaceutical sector is looking for a Shift Laboratory Analyst to conduct quality control analyses. The role requires precision in analytical methods and adherence to regulatory standards. Candidates should possess a relevant degree and have extensive laboratory experience, particularly in HPLC. The analyst will ensure compliance with GLP standards and maintain high-quality analytical services while meeting reporting deadlines.

Qualifications

• Minimum 5 years laboratory experience, including HPLC expertise.

Responsibilities

• Perform analytical tasks including chromatographic analysis and dissolution testing.
• Validate analytical methods and assist in method development.
• Maintain compliance with Good Documentation and Laboratory practices.

Skills

Communication

Analytical Skills

Teamwork

Education

Diploma or Degree in Analytical Chemistry

Tools

HPLC

Job description

Shift Laboratory Analyst

Reference: JHB-Sines-1

Our client is seeking a Shift Laboratory Analyst responsible for conducting quality control analyses in accordance with the Quality Management System and South African Health Products Regulatory Authority requirements. The role involves performing analytical methods, adhering to standard operating procedures, and reporting results with high precision and accuracy to ensure high-quality analytical services.

The analyst will meet reporting deadlines for various samples/commodities, maintain confidentiality, and perform duties aligned with GLP standards within a pharmaceutical analytical environment.

Responsibilities

1. Perform analytical tasks as assigned, including chromatographic analysis, dissolution testing, IR, UV, titrations, and physical tests.
2. Validate analytical methods and assist in method development in collaboration with senior analysts and management.
3. Complete and maintain accurate logbooks and calibrate apparatus according to SOPs and calibration programs, verifying standards and calibration dates.
4. Ensure deviations are authorized by QA Manager or responsible persons and maintain compliance with Good Documentation, Manufacturing, and Laboratory practices.
5. Prepare reagents accurately, document procedures and results, and ensure data integrity following ALCOA guidelines.
6. Maintain laboratory cleanliness, participate in safety procedures, and adhere to health and safety policies.
7. Perform other duties as assigned by management, ensuring productivity and meeting key performance indicators.

Qualifications & Experience

• Relevant Diploma or Degree in Analytical Chemistry or equivalent.
• Minimum 5 years laboratory experience, including HPLC expertise.

Skills

• Strong verbal and written communication skills.
• Deadline-oriented with a focus on quality.
• Ability to work under pressure and as part of a team.
• Detail-oriented with excellent analytical skills.