Assistant Manager - Singapore - ABIORES PTE. LTD.

ABIORES PTE. LTD. Singapore

18 hours ago

Description

Roles & Responsibilities

Assistant Manager / Manager, Quality Assurance

About CorDx:

CorDx is a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,000 employees across the world, serving millions of users in over 100 countries.

CorDx is transforming the global diagnostics industry with innovative R&D solutions, a vertically integrated supply chain, and manufacturing footprints in the United States and around the world.

With nearly two decades of IVD experience, CorDx is a leader in IVD research and development, manufacturing, and supply chain. Our proprietary line of rapid diagnostic products is recognized by families and medical professionals for reliability, affordability, and rapid results.

CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious disease such as COVID-19, pregnancy, drugs of abuse, biomarkers, and more. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare.

Job Responsibilities

Implement, manage and constantly improve the company's quality management system, including but not limited to the IVD products and equipment;
Regularly perform internal audits, compile audit reports, problem analysis reports, improvement proposals, and monitor the rectification plan and its implementation;
Lead and Participate in the internal audits and management reviews of the company's quality system as key member of company's quality department;
Manage the system and documents of company's quality management system, including but not limited to the IVD products and equipment;
Be specifically responsible for the IVD equipment quality management system;
Statistical analysis of IVD equipment quality data, and draft reports and corrective and preventive measures;
Update quality standards, laws and regulations and publish company quality policy;
Establish collaborative and cooperative working relationship with key opinion leaders and the regulatory bodies;
Collaborate with cross-functional teams to meet projects goals with overall organizational objectives.
Any other ad-hoc duties or projects as required by the management team.

Qualifications:

Quality system related training and internal auditor training;
Familiar with ISO9000 & ISO13485 quality management system and certification work, experience with successful case(s) will be preferred;
Familiar with GMP and medical device industry standards and specifications;
Strong quality management system knowledge and capabilities;
A bachelor's degree with 7 years of relevant experience, a master's degree with 3 years of relevant experience, or a doctorate degree with at least 1 year of relevant experience. Others are welcome to apply.
Familiar with in vitro diagnostic products such as lateral flow immunoassay, PCR, Immunoassay etc;
Familiar with IVD product development and commercialization life cycle;
Systematical project management, good planning, execution and timely communication. Good presentation skills.
Majoring in biology, medicine, laboratory science, immunology, pharmacy or quality engineering are preferred;
Enthusiastic, proactive, and down-to-earth work attitude, strong communication & execution ability, results driven, and a team player;
Meticulous and strong sense of responsibility; able to handle stress and tight schedule;

How to Apply:

Please send a comprehensive resume, a cover letter (if applicable), along with your current and expected salary to or click to submit here @ My careerfuture.
We regret that only shortlisted candidates will be contacted

Tell employers what skills you have

Biomarkers
Quality Management
Quality Assurance
Quality System
Global Health
Supply Chain
GMP
in Vitro
Reliability
Auditor
Quality Engineering
Audits
Presentation Skills
Product Development
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