Summary
Date Posted: Friday, August 16 2024, Base Salary: Not Disclosed

JOB DETAILS:
Quality Plastics (U) LTD is seeking a highly skilled and experienced Quality Assurance Officer to ensure the facility’s overall compliance, premises, processes, methods, equipment, utilities, and axillary units to current Good Manufacturing Practices (cGMP). To make organized arrangements in totality and ensure that products being manufactured meet prescribed quality levels for their intended use throughout the production chain.
If you are performance-driven, possess exceptional organizational and planning skills, excel in problem-solving, and have the ability to motivate others, we would want to hear from you.

Key Responsibilities.
• Author QA SOP, reviewer of SOPs, and Approve of SOPs within the scope of QMS, Author Batch Manufacturing Records
• Change Control documentation, review, and approval.
• Deviation documentation, review, and follow-up on the closure or even closure of deviations
• Factory Nonconformity investigation and CAPA handling, implementation follow up and verification of action(s) effectiveness
• Oversee the cleanliness of production premises, ensure that sanitization points have a sanitizer, the disinfection points have a disinfectant with known concentrations.
• Equipment registration, identification, and labelling
• Equipment qualification and validation of systems.
• Issuance and control of BMR and quality labels and Batch numbers
• Approval of executed BMR and authorization of finished product release.
• Control of all executed BMR
• Preparation of protocols for Equipment qualification and validation of methods, processes, and systems.
• Internal audit coordination and self-inspection implementation
• Control of documents accessibility and availability, keeping track of working and obsolete documents
• Developing and keeping track and follow-up schedules for equipment calibration, medical examination, training, validation, internal audits, microbial water sample collection, preventive maintenance,
• Coordinating training activities and participating in the training of personnel on specific topics of cGMP
• Trending of the key process critical activities and equipment performance, environment humidity, and Temperature.
• Perform product quality reviews and give technical advice on process performance improvement.
• Monitoring the ALCOA+ Adherence and ensuring that data integrity is maintained
• Handling of complaints for both inputs to QPL (complaints to vendors and suppliers) & complaints related to QPL outputs (our customer’s complaints regarding our products) and giving feedback to customers (where necessary)
• Ensuring that personnel is inappropriate PPE while performing manufacturing activities.
• Ensuring compliance to good production practices and ensuring that unauthorized items are not allowed in the facility e.g., earrings, jewellery, lipstick, phones, etc.
• Process validation
• Generating URS for key equipment, material, and packaging material
• Assisting in writing QA respective factory monthly report
• Materials inspections

Requirements
• Minimum Experience :1 year experience in a busy manufacturing plant under Quality Assurance
• Minimum Education: Bachelors Degree in Science, Technology Chemistry or Pharmaceuticals
• Basic knowledge in English (verbal and written)

Work Hours: 8

Experience in Months: 12

Level of Education: Bachelor Degree

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