Qms Document Controller Executive

Responsibilities Establish and enforce document control policies and procedures aligned with company QMS for Singapore operations. Receive, review, register and distribute incoming/outgoing documents (drawings, contracts, SOPs, regulatory filings) across internal teams and external parties. Maintain strict version control, naming conventions, controlled...

Our vision is to transform how the world uses information to enrich life for all.Join an inclusive team passionate about one thing: using their expertise in the relentless pursuit of innovation for customers and partners. The solutions we build help make everything from virtual reality experiences to breakthroughs in neural networks possible. We do it all...

Competency Requirement - Bachelor of Engineering or equivalent or higher - 10 years’ experience in Quality Assurance - 5 years’ experience in QMS such as MDR, EN ISO 13485, FDA 21 CFR 820 - Certified ISO 13485 Lead Assessor **Responsibilities**: - Perform activities related to the documentation of Quality Management System (QMS) and ensure relevant...

Industry/ Organization Type: Manufacturing - Position Title**:Document Controller**: - Working Location: Joo Koon - Working Hours: 5 days (8am-5.30pm) - Salary Package**:Basic Salary $2,800 + Variable Bonus**: - Duration: Permanent **Key Responsibilities** - Track and manage document revisions to ensure only the latest versions are in use. - Coordinate...

**Primary Job Responsibilities**: - Sustain an active Quality Management System, such as Management Review, Internal Audit, CAPAs, NCRs, Document Control, Change Control, Risk Management and Training. - Establishes, reviews, maintains and improves quality documents (e.g., SOPs, specifications, methods, records, etc.) to ensure compliance with ISO 13485, MDR...

Job Description Industry/ Organization Type: Manufacturing Position Title: Document Controller Working Location: Joo Koon Working Hours: 5 days (8am-5.30pm)Salary Package: Basic Salary $2,800 + Variable Bonus Duration: Permanent Key Responsibilities Track and manage document revisions to ensure only the latest versions are in use. Coordinate document review...

Overview The Quality Management System(QMS) and Regulatory Manager is responsible for the operational leadership and oversight of the organization’s QMS and regulatory compliance functions. This individual serves as the QMS Management Representative in accordance with ISO 13485 and as the Person Responsible for Regulatory Compliance (PRRC) under the EU...

1. Preparation and revision of QA SOPs and always keep it current. 2. Review SOPs and Work instructions of other departments and verify compliance. 3. Issuance, retrieval and tracking of QMS documents across the site. 4. Tracking and facilitating timely completion of QMS events (e.g., Change control, deviation, OOS, CAPA) and related documentation. 5....

European MNC with manufacturing of medical parts Location: Ang Mo Kio Area 5 day work week - Collaborate with internal stakeholder and customers on inspection, testing, process capability support and inspection plans - Own nonconformance issues raised and drive for disposition, investigation, CAPA and customer communication - Lead in ERP and QMS System -...

Regulatory Affairs & QMS Manager Reporting to the Chief QARA Officer (Based in Singapore), you will be responsible for: Regulatory Affairs & Compliance Serve as the Person Responsible for Regulatory Compliance (PRRC) under Article 15 of the EU MDR for full or selected scope of responsibility. Interpret and apply global medical device regulations and...