Job Openings at Nurture Brands

Responsibilities:

• Analysis of raw materials as allocated by the QC Supervisor: on time and according to specification.
• Analysis of tablet intermediate products and fill oils as allocated by the QC Supervisor: on time and according to specification.
• Performing water sampling and testing: on time and according to specification.
• Accurate completion of all test reports in compliance with GLP requirements.
• Capturing of data to be done timeously and accurately.
• Assisting in the compilation and review of SOPs.
• Perform GLP roster testing timeously and accurately.
• Assist with analytical investigations as required.
• Maintaining appropriate levels of GLP and hygiene in the laboratory at all times.
• To assist with waste disposal as required
• To assist with equipment maintenance and qualification as required.

Requirements:

Essential:

• National Diploma in Chemistry or Food Science or BSc with Chemistry or equivalent.
• Computer literacy (MS Word, MS Excel, Powerpoint).
• Knowledge of GLP,GMP

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Responsibilities:

• Perform line opening/Closing as per SOP and ensure that the areas and equipment are clean and that only components and products related to a specific batch are being issued.
• Continuous monitoring of production areas to ensure SOP and GMP compliance in all aspects of production.
• Ensure that the quality of products produced complies with the Company’s Policy and specifications.
• Report on GMP compliance and non-compliance in all production areas.
• Initiate and review of operating procedures to govern process ensuring compliance.
• Initiate and review deviations, investigations, incident reports, risk assessments and other related documentation. 
• Documentation review - check all product batch related documentation before and after manufacturing and packaging when required.

Requirements

Essential:

•  Grade 12 certificate
•  Post Basic Pharmacist Assistant: Registration at the SA Pharmacy Council.

Desired:

•  Previous experience in Pharmaceutical manufacturing.

go to method of application »

Responsibilities:

• Aid in the production and manufacturing of pharmaceutical products according to established protocols and guidelines.
• Assist with quality control checks to ensure product integrity and compliance in line with regulatory standards
• Perform line opening/Closing as per SOP. Ensure that the areas and equipment are clean and that only components and products related to a specific batch are being issued.
• Continuous monitoring of production areas to ensure SOP and GMP compliance in all aspects of production.
• Ensure that the quality of products produced complies with the Company’s Policy and specifications.
• Report on GMP compliance and non-compliance in all production areas.
• Initiate and review of operating procedures to govern process ensuring compliance.
• Initiate and review deviations, investigations, incident reports, risk assessments and other related documentation. 
• Documentation review - check all product batch related documentation before and after manufacturing and packaging when required.

Requirements

Essential:

• Bachelors Degree in Pharmacy or related field.
• Valid pharmacy license or certification
• Strong understanding of pharmaceutical production and manufacturing processes
• Knowledge of current good manufacturing (cGMP) and other regulatory guidelines
• Excellent attention to detail and ability to follow strict protocols and procedures.
• Good organizational and time management skills
• Strong communication and interpersonal skills
• Ability to work well in a team and collaborate with cross-functional departments.
• Prior experience in a pharmaceutical production or manufacturing setting is a plus
• Proficiency in Microsoft Office Suite and other relevant software applications.