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.

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.