Total 5 quality assurance job vacancies in Singapore

• Reputable Data Centre in Singapore
• Global coverage

About Our Client

My client is a leading global data center provider known for delivering secure, high-performance infrastructure solutions to support the digital operations of businesses worldwide.

Job Description

• Keep the Quality Management System effective, following company's guidelines and certification standards.
• Handle Data center certification strategy and plan for audits.
• Perform internal audits to meet internal and global standards.
• Coordinate external certification audits as per the plan.
• Maintain a central database to track issues and improvements found in audits, identify the causes, and ensure timely resolutions.
• Work to bring different management systems under one Integrated Management System for better efficiency and certification compliance.
• Continuously update instructional documents for the QMS.
• Keep the document management system organized and up to date.
• Track and report key performance indicators (KPIs) for quality.
• Assist the Senior Director of Quality & Accreditation with regular reporting and management reviews.
• Help other departments maintain high-quality standards and support them with client requests and audit

The Successful Applicant

• Bachelor degree holder or equivalent professional experience in Data Center industry
• Strong knowledge of management systems and related certifications in Data Center
• 5 years+ of relevant experience in quality management.
• Ability to work well in an international team environment.

What's on Offer

• Attractive package will be offered to the right candidate.

Contact

Hazel Choi (Lic No: R24122391 /EA no: 18S9099)

Quote job ref

JN-102024-6557651

Phone number

+65 6533 2777

Michael Page International Pte Ltd | Registration No. 199804751N

• To join a Global Engineering Company
• Exposure to industrial trends and technology

About Our Client

The client is a global engineering company specializing in environmental systems, HVAC (heating, ventilation, and air conditioning), and industrial paint finishing systems. The company is renowned for its innovative solutions in air quality control, energy efficiency, and cleanroom technology, particularly in sectors such as automotive, electronics, pharmaceuticals, and semiconductors. With a strong focus on sustainability and process automation, the company serves industries across the world, offering tailored engineering services and systems that improve operational efficiency and environmental performance. The company also emphasizes compliance with international standards like ISO and QS, positioning itself as a leader in industrial engineering and quality management.

Job Description

Responsibilities

• Visualize and map business processes to identify inefficiencies and bottlenecks.
• Develop and implement SOPs for consistent practices across departments.
• Lead automation initiatives, including Robotic Process Automation (RPA) and paperless processes.
• Define performance indicators and regularly review them to enhance operational efficiency
• Implement a culture of continuous improvement using the Plan-Do-Check-Act (PDCA) cycle across local entities.
• Regularly review processes and propose improvements based on performance data.
• Facilitate ongoing training for staff on new systems, improvement methodologies, and leadership skills.
• Promote the use of digital communication platforms (e.g., Microsoft Teams) to enhance teamwork and information sharing.
• Conduct risk assessments and ensure compliance with legal and regulatory standards, focusing on information security.
• Regularly audit and update compliance processes in response to business and legal changes.
• Implement and maintain a knowledge management system to accumulate and share internal knowledge across the region.
• Standardize document creation, storage, version control, and archiving processes to improve efficiency and security.

The Successful Applicant

Skills & Experience Required

• Proven experience in business process improvement and quality management (ISO/QS).
• Strong knowledge of document management systems and business standardization.
• Expertise in IT systems (ERP, CRM) and digital tools for process optimization.
• Strong data analysis and evaluation skills.
• Familiarity with legal regulations and compliance standards.
• Excellent communication, leadership, and training abilities.
• Experience in change management and cultural adaptability in a regional/global setting.

What's on Offer

The company offers an exciting opportunity to be part of a global leader in engineering solutions. Candidates will have the chance to play a crucial role in shaping operations across Southeast Asia and South Asia, contributing to the growth and standardization of the company's processes in these regions. The company provides a dynamic work environment focused on innovation, continuous improvement, and sustainability. Employees will benefit from exposure to advanced technologies in quality management and automation, professional development opportunities, and the chance to collaborate with a diverse and skilled global team. Additionally, the company's commitment to ISO and QS standards ensures a structured and high-performing environment, allowing individuals to develop expertise in industry-leading practices.

Contact

Timothy Huang (Lic No: R1980928/ EA no: 18S9099)

Quote job ref

JN-102024-6569887

Phone number

+65 6416 9863

Michael Page International Pte Ltd | Registration No. 199804751N

• Be part of a visionary company transforming healthcare and empowering innovation
• High visibility role with empowerment to create direct impact to the business

About Our Client

They are a pan-Asian brand with a longstanding history in the market, having been selling across Asia for decades. Their medicine is the bestselling in its category due to its efficacy and strong brand recognition. They are currently seeking a highly skilled and experienced Quality Control (QC) Manager to ensure that all pharmaceutical products meet the organisation's quality standards and regulatory requirements before commercialisation.

Job Description

• Oversee and conduct testing of raw materials, APIs, finished goods, and stability samples to ensure adherence to quality standards
• Lead and mentor a team of QC analysts, ensuring alignment with quality goals, providing training, and offering technical support when necessary
• Review, validate, and approve laboratory data, ensuring accuracy, precision, and reliability of results
• Develop and implement new testing methods and ensure team adherence to industry standards and regulatory guidelines
• Act as a liaison between the QC team and cross-functional teams including Production, Quality Assurance, and Regulatory Affairs to resolve quality issues
• Lead investigations into out-of-specification results, deviations, and customer complaints, ensuring root cause analysis and effective corrective/preventive actions (CAPAs) are taken
• Monitor manufacturing processes to ensure adherence to product specifications, and proactively address potential quality risks
• Collaborate with senior management to develop strategies for improving quality control processes and implementing best practices
• Ensure compliance with regulatory requirements (FDA, EMA, ICH etc.) by preparing comprehensive reports and maintaining up-to-date documentation for internal and external audits
• Ensure laboratory equipment is maintained, calibrated, and ready for accurate testing operations
• Support continuous improvement initiatives and lead team projects aimed at optimizing quality control processes

The Successful Applicant

• Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related discipline
• Experience in a quality control or analytical laboratory, preferably in the pharmaceutical manufacturing industry, preferably from an oral solid dosage formulation plant
• Strong knowledge of Good Manufacturing Practices (GMP), International Conference on Harmonisation (ICH) guidelines, and regulatory requirements such as FDA
• Expertise in analytical techniques such as HPLC, GC, UV-VIS, and FTIR
• Excellent problem-solving, decision-making, and troubleshooting abilities
• Ability to work effectively in a fast-paced, regulated environment
• Demonstrate excellent communication skills, ability to effectively present strategies and solutions with stakeholders/ cross-functional teams

What's on Offer

This opportunity offers a dynamic environment where you can continually grow and push your capabilities to greater height. You'll be part of a team that values your contributions and is committed to your growth and development.

Contact

Vanessa Chan (Lic No: R2197577/ EA no: 18S9099)

Quote job ref

JN-102024-6553996

Phone number

+65 6643 9742

Michael Page International Pte Ltd | Registration No. 199804751N

• Global Corporation
• Exciting Career Development

About Our Client

Our Client is a global company that provides a wide range of business services, focusing on products and services related to apparel, safety supplies, and facility services. With their ever-expanding portfolio in providing services for their customers, they aim to maintain and improve their current performance both locally and regionally of which they are seeking a Supply Chain Quality Assurance/ Social Compliance Specialist (Apparel) to be based at their HQ in Singapore.

Job Description

You will be reporting to the Head of Department directly. The majority of your responsibilities will include meeting with various suppliers to ensure safety and quality compliance, supply chain process improvements and product development.

Your responsibilities include:

• Policy Adherence: Ensure compliance with company policies and procedures, including those related to supplier management and internal communication.
• Internal Communication: Regularly update Global Supply Chain Partners on support status, projects, and issues through monthly and weekly reports. Conduct root cause analysis of supplier problems and communicate findings to leadership.
• Product Quality: Support product quality through analysis and inspections, maintaining understanding of computer systems and procedures, and collaborating with suppliers to meet quality specifications.
• Vendor Start-Ups: Assist with vendor start-ups, coordinating with planning teams on volume needs and ensuring product specifications and quality standards are met before production.
• Social Compliance: Perform social compliance audits, follow up on audit items, and address social compliance non-conformance at suppliers.
• C-TPAT Compliance: Ensure proper security measures are in place for C-TPAT certified vendors and plants.
• Safety and 6-Sigma Training: Provide input for safety improvements based on OSHA training, and offer 6-Sigma training as requested and applicable.
• Process Improvement: Recommend process improvements to vendors and plants to enhance cost, quality, and delivery. Suggestions may include organizational improvements, in-line controls, and efficiency studies.
• Engineering Support: Conduct GSD analysis, increase productivity, and reduce labor costs through improvements in work methods, process controls, and throughput time. Provide support for costing analysis and evaluate preventative maintenance programs.

The Successful Applicant

You should have at least a Degree in Logistics/Supply Chain or Engineering related fields and experience in supply chain process improvements and corporate health and safety compliance. You must possess strong analytical and reporting capabilities. It is essential that you have been exposed to Six Sigma Lean Belt training and have done quality assurance improvement processes. You will need to have great communication skills to work closely with vendors. Travelling is required for this role and prior experience in a garment manufactuing/ factory setting is a pre-requisite.

What's on Offer

You will be working in a large organization that has good brand equity and consistently innovating for consumers. The company recognizes talents by offering comprehensive benefits and extensive training to nurture employees & provide you with excellent career advancement. The company culture is about high levels of commitment and care for employees that helps achieve an effective mix between work and home life and supports their efforts to have a positive impact on their communities. They also place a lot of emphasis in workplace safety and employee welfare.

Contact

Shangari Manoharan (Lic No: R21101201/ EA no: 18S9099)

Quote job ref

JN-022024-6336783

Phone number

+65 6643 9733

Michael Page International Pte Ltd | Registration No. 199804751N

• Global MNC, Market leader in Pharmacuetical Industry
• Dynamic and professional development-oriented environment

About Our Client

The client is a global pharmaceutical and healthcare organisation. They are a leading player in the industry, known for its extensive research and development efforts in the fields of pharmaceuticals, biotechnology, and healthcare solutions. With a strong commitment to innovation, they aim to improve patient care and well-being through the discovery and development of a wide range of medical treatments, including prescription drugs, generics, and cutting-edge therapies. They have a significant global presence and a diverse portfolio of products, spanning from pharmaceuticals to generic medications. Currently, they are looking for Quality Control Manager to join their team.

Job Description

• Optimise workflow efficiency and procedures, assist in validation procedures and reports
• Establish quality systems for the QC Raw Material lab in compliance with regulations
• Ensure timely document review and testing, implement production tracking systems to facilitate raw material quality testing and evaluation
• Manage budgeting and resource planning
• Manage global stakeholders
• Address deviations and propose corrective actions, review QA/QC documents to ensure compliance with specifications and regulations
• Improve test procedures for enhanced efficiency, provide technical support to various departments, and train QA/QC staffs on new methodologies and instrumentation

The Successful Applicant

• Bachelor Degree in Biologics, Chemistry, Pharmaceutical, Chemical Engineering or relevant field
• Experience with Quality Control Raw Materials processes within biopharmaceutical industry
• Strong leadership skills
• Strong in stakeholder management and equipped with business and financial acumen
• Prior knowledge of regulatory requirements, along with familiarity with industry tools and systems
• Demonstrate good understanding of cGMP, knowledge of manufacturing, quality control and validation requirements and activities

What's on Offer

• Dynamic, collaborative and engaged workplace culture
• Attractive renumeration package with great career advancement opportunities
• Strong leadership team