- No. 30, Jalan Tasik Selatan 3, Bandar Tasik Selatan Sungai Besi WP Kuala Lumpur Malaysia 57000

工作地点
职位描述
任职资格
Fresh graduates are encouraged to apply.
Good communication skills in English and Bahasa Malaysia.
Good organisational skills and attention to detail when handling quality documentation and records.
Able to prepare, maintain and update quality-related documents accurately.
Good communication and coordination skills when working with internal departments and external parties.
Willing to learn quality assurance procedures, audit processes and regulatory compliance requirements.
Responsible, proactive and able to work independently as well as in a team.
岗位职责
Document Control
Assist in managing the quality document control system.
Prepare and revise Quality Procedures for process owners.
Prepare Document Change Notices (DCN).
Issue documents with proper identification, including Master Copy, Controlled Copy, Uncontrolled Copy and For Training Purpose Only.
Update and maintain the Document Master List and Records Master List, and control document distribution within the Quality & Regulatory Compliance Management System (QRCMS).
Maintain Master Copies, Controlled Copies and obsolete documents.
Technical Documentation
Assist in preparing and maintaining Technical Documentation in accordance with EU MDR 2017/745 requirements.
Liaise with OM to obtain updated Technical Documentation periodically.
Audits
Assist in planning and coordinating Supplier / OM periodic evaluation audits.
Participate in internal audits, Supplier / OM periodic evaluation audits and external audits.
Compile and maintain audit files and related documentation.
Design and Development
Communicate with OM to assess the feasibility of new designs or modifications to existing designs.
Coordinate with cross-functional teams, including Sales and Marketing, QA, QC and RA, to align design and development project objectives.
Prepare design plans and monitor project timelines.
Prepare Sample Requisition Forms for Design and Development (SRD).
Organise review meetings with team members at each stage of design and development.
Conduct product verification and validation to ensure compliance with applicable requirements.
Complete and maintain design and development files.
Artwork Verification
Check, review and verify medical device packaging labels to ensure compliance with customer requirements and applicable regulatory requirements.
Liaise with suppliers, designers and OM regarding artwork amendments and conversions.
Coordinate with customers for artwork amendments and approvals.
Compile and maintain artwork files.
Other Responsibilities
Participate in the Risk Management Team.
Assign GS1 barcode numbers for new or modified items.
Assign lot numbers for legal manufacturer's products.
Perform other work-related duties as assigned by the superior.
好处
MRT - SERDANG RAYA UTARA
0.9 km
MRT - SUNGAI BESI
1.6 km
LRT - SUNGAI BESI
1.6 km
LRT - BUKIT JALIL
1.8 km
重要安全守则
申请工作时,切勿提供您的银行或信用卡详细资料。不要转账或完成无关的在线调查问卷。如果您发现可疑内容,请举报此招聘广告。