Jobs Available at Nurture Brands

Key Responsibilities:

• Assist in reviewing and updating standard operating procedures (SOPs)
• Support internal audits and documentation reviews.
• Help maintain quality management systems (QMS) and records.
• Participate in deviation, CAPA (Corrective and Preventive Action), and change control processes.
• Collaborate with cross-functional teams including R&D, Production, and Regulatory Affairs.
• Assist in data collection and report preparation for quality metrics.

Qualifications:

• Qualification in Pharmacy, Life Sciences, Chemistry, or related field.
• Strong attention to detail and organizational skills.
• Basic understanding of GMP, GLP, or other regulatory standards (preferred).
• Proficient in Microsoft Office (Word, Excel, PowerPoint).
• Excellent written and verbal communication skills.Ability to work independently and as part of a team

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Description

• Amend and create Bills of Materials (BOMs) and Process/MES templates in line with change requests and new product developments.
• Liaise with suppliers to gather and verify documentation for approval of new or alternative raw and packaging materials.
• Compile and process approval documentation in accordance with manufacturer, supplier, and material approval procedures (QA28).
• Initiate non-technical deviations as required by Planning and Production.
• Maintain accurate administration and filing of completed projects and records.
• Create and manage gelatine colour masters for all relevant products.
• Raise requisitions and coordinate outsourced analytical testing and raw material procurement for trials.
• Manage and maintain primary reference standards for QC and PD laboratories.
• Coordinate with PD Chemists to create and finalise Analytical Procedures for raw materials and finished products.
• Liaise with Halal certification authorities (MJC) for raw material approvals.
• Foster a positive work environment, engage in ongoing professional development, and ensure adherence to best practices.

Requirements

• National Diploma in Analytical Chemistry (B.Sc. advantageous).
• Minimum 1 year in an administrative role (pharmaceutical/lab experience preferred).
• Knowledge of Syspro, GMP, QMS, and Change Control Records.
• Proficient in MS Word, Excel, and PowerPoint (Syspro experience beneficial).