Job Description

Fine Chemicals requires the services of a highly competent ADD Supervisor for the Analytical Development Department. To qualify for this position the most suitable candidate must fulfill the following requirementsJOB REQUIREMENTS:

• National Diploma or Bachelor of Science Degree in Analytical Chemistry or equivalent
• A minimum of 5 years experience in a pharmaceutical laboratory with at least 2 years in a leading role.
• Experienced in the practical application of analytical test methods, instrumentation software, troubleshooting, and data processing, especially related to chromatography would be advantageous
• Ability to design and coordinate execution of the method validation experiments
• Knowledge and experience in cleaning validation procedures.
• Understanding of reference standard qualification and inventory management.
• Good knowledge and understanding of GLP (Good Laboratory Practice).
• Experience in or knowledge of the API testing environment would be an added advantage
• Technologically proficient working with various software platforms i.e., Power BI, MS Office, ERP Systems, LIMS

BASIC JOB TASKS INCLUDE BUT NOT LIMITED TO THE FOLLOWING: * Deliver comprehensive analytical support to internal and external stakeholders.

• Develop, implement, and maintain the cleaning validation program.
• Manage the qualification and administration of reference standards.
• Maintain rigorous GLP compliance, including meticulous documentation of results, thorough investigation and reporting of Out-of-Specification (OOS) events, and safe handling and disposal of laboratory materials.
• Ensure all personnel meet the required training standards.
• Execute all assigned tasks according to established training protocols.
• Maintain and enforce GLP standards throughout the laboratory.
• Develop and train team members, manage employee performance, and timekeeping, recruitment of staff, and maintain staff discipline in accordance with the company disciplinary SOPs / code of conduct.
• Adhere to all Company Occupational Health, Safety, and Environmental (OHSE) rules and regulations.
• Ensure all activities comply with Good Manufacturing Practice (GMP) requirements as outlined in Company Standard Operating Procedures (SOPs) and written instructions.

PERSONAL ATTRIBUTES (Brief Summary): * Strong time management and planning abilities.

• Excellent problem-solving and analytical skills.
• Service-oriented mindset.
• Proven team player, quality-conscious, trustworthy, flexible, and detail-oriented.
• Knowledge of relevant processes and systems.
• Exceptional attention to detail and accuracy.
• Effective written and verbal communication, including report writing and document review.
• Proficiency in operating laboratory equipment and critically evaluating data.
• Availability for after-hours and overtime work as needed.

Suitably qualified applicants are invited to submit their CVxe2x80x99s online on or before the specified date. Preference will be given to applicants from designated groups in accordance with laws governing employment equity, where such laws are applicable to the Aspen entity that will employ the successful candidate. If you have not heard from the HR department within 30 days of this advert closing, please consider your application unsuccessful.

Aspen Pharmacare