Quality System Executive/ QA Executive
2 weeks ago
5 days work week - Location: North/North East - Basic up to $5500 - AWS & VB provided **Job Scope**: **Quality System Engineer - Electronic, PCBA** - Oversee implementation of various management systems and business accreditations. - Maintain and ensure appropriateness of Quality Manuals and Procedures. - Analyze current and future procedural needs of the business. - Manage the internal audit system and corrective action reporting system. - Conduct Quality Systems audits and train/guide other auditors. - Host external Quality System audits. - Review Quality procedures related to plant improvement initiatives. - Maintain Standard Operating Procedure content and coordinate issuance. - Collect quality data for monitoring targets. - Assist with quality awareness training. - Undertake special projects as required. - Ensure quality control through appropriate reviews. - Support/lead process and continuous improvement activities. - Manage and monitor equipment calibration. - Coordinate with Outsource Management for subcon selection and approval. - Establish and improve subcon quality assurance and development system. - Perform audits on new and existing subcons for quality evaluation. - Involved in new production introduction and product transfer to subcon. - Manage Corrective Action Report process and resolution. - Work with subcons on customer complaint 8D. - Develop and maintain policies to measure and ensure subcon performance. - Monitor key quality metrics (Subcon OTD, system, process audit, yield). - Establish sampling plan and testing criteria for incoming, site inspection or subcon production. **Quality Assurance Executive - Biolifescience/Pharmeceutical** - Collect necessary data for management reports on quality metrics and create relevant sections of the reports. - Compose and distribute Standard Operating Procedures (SOPs) for site qualification and validation projects whenever necessary. - Detect deviations and potential risks in manufacturing systems, processes, and methods, along with their potential causes. - Execute validation procedures to assess the systems, methods, and processes employed in manufacturing facilities. - Assess the impact of project changes on validation and define suitable validation requirements and approaches to meet these requirements. - Identify potential gaps and compliance risks and provide recommendations for improvements. - Evaluate and authorize validation deliverables related to Facility/Utilities/equipment, computerized systems (automation), and laboratory equipment/systems to ensure adherence to company procedures, regulatory requirements, cGMP expectations, and project schedules. - Collaborate with counterparts to manage site change control and deviations in order to meet project deadlines. - Ensure adherence to Safety, Health, and Environmental (SHE) requirements at the site. **Job Requirement**: - Relevant quality assurance/management experience Electronic Manufacturing Industry in related to PCBA - OR Relevant quality assurance/management experience in Bio-lifescience/Pharmeceutical Industry - Minimum >2 years relevant experience in related Quality Assurance / Quality Management To Apply, kindly click on the "APPLY NOW" button Staffking Pte Ltd (20C0358) | Chong Kar Ming (John) (R21101412)
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