Regulatory Affairs/Quality Assurance APAC

NEVEON Executive Committee; Singapore; Sur place; SGD 90 000 - 150 000; Plein temps

Résumé du poste

Greiner Bio-One Singapore Pte. Ltd. is seeking a Regulatory Affairs / Quality Assurance professional to support APAC regulatory compliance, registrations and QA activities.

You will link regional markets with global functions to ensure products meet regulatory and quality standards. The role requires coordinating with local authorities, distributors and internal teams, handling registrations and audits, and advising on regulatory changes across APAC.

Qualifications

• Bachelor's degree in Life Sciences or related field.
• 3–5 years in medical device or IVD regulatory work preferred.
• Familiar with APAC regulatory frameworks (HSA, TGA, NMPA, PMDA, TFDA).
• Knowledge of the MDSAP Audit programme is an advantage.
• Strong analytical and documentation skills; good stakeholder management.

Responsabilités

• Manage regulatory applications, renewals and licenses for APAC markets.
• Coordinate with regional partners and HQ on registrations and compliance.
• Act as expert on regulatory requirements across APAC regions.
• Maintain regulatory documentation and update the registrations database.
• Support internal audits and regulatory inspections by authorities.
• Assist design changes and post-market incident processes.
• Monitor and respond to regulatory changes affecting APAC markets.

Connaissances

Regulatory affairs

Quality assurance

Stakeholder management

English communication

Regulatory intelligence

Formation

Bachelor's degree in Life Sciences / Pharmacy / Biomedical Engineering

Description du poste

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We are not offering you a job, but rather we are offering you aworkplace that feels like home at Greiner Bio-One.

Regulatory Affairs/Quality Assurance APAC

Location:

Singapore, SG, 068902

Employment Type: Permanent

We are looking for a Regulatory Affairs / Quality Assurance professional to join Greiner Bio-One Singapore and support regulatory and quality activities across the Asia-Pacific (APAC) region.
In this regional role, you will work closely with local subsidiaries, distributors, and global Regulatory Affairs and Quality Management teams to support regulatory compliance, product registrations and quality-related activities across APAC markets. You will serve as an important link between regional markets and Greiner Bio-One's global functions, helping to ensure that products are compliant with applicable regulatory requirements and maintained to the company's quality standards.

Core Responsibilities:

• Manage the application, renewal and maintenance of GBO-APAC local countries’ product registration and licenses; coordinate and work closely withGBO-APAC market authorized holders and GBO headquarters
• Regularly coordinate and liaise with internal stakeholders, GBO-APAC business partners, and local authorities/regulators
• Act as the Medical Devices Regulatory and Compliance Subject Matter Expert in APAC; beaware of and monitor global and local regulations and standards changes and provide advice onlocal andregional requirements
• Maintain regulatory documentation and ensure theregistration database is updated
• Support and assist internal/external audits; participate in regulatory inspections by the external authorities/regulators
• Support, assist and provide advice of product design changes and control processes
• Support, process and manage product incidence reports, post-market
• Ensures complaints are processed and documented according to regulatory requirements
• Ensures complaints are investigated in due time and work cross-functionally with HQ on prioritization
• Assist in implementing and maintaining thelocal QMS, training system and related procedures.
• Support and coordinate monitoring and review of issues, customer dissatisfaction, and complaints received for APAC

Your Profile

• Bachelor’s Degree in Life Sciences, Pharmacy, Pharmaceutical Sciences, Biomedical Engineering, or a related scientific discipline.
• Minimum 3-5 years of experience in medical device or IVD product registration ispreferred.
• Familiarity with national health authority registration frameworks across APAC (e.g., HSA in Singapore, TGA in Australia, NMPA in China, PMDA in Japan, TFDA Taiwan, ASEAN Medical Device Regulatory Framework).
• Familiarity with the MDSAP Audit programme.
• Strong analytical, organisational and documentation skills with excellent attention to detail.
• Good communication and stakeholder management skills, with the ability to work effectively across different cultures and countries.
• Ability to manage multiple projects and regulatory timelines independently.
• Proficiency in English; additional Asian languages would be an advantage.

Our Offer

Company Overview:

Greiner Bio-One Singapore Pte. Ltd. is part of Greiner Bio-One, a globally active medical technology company for the in-vitro diagnostics, biotechnology, diagnostic and pharmaceutical industries. The broad portfolio is sold in more than 100 countries worldwide. By using state-of-the-art technologies, Greiner Bio-One creates the basis for top performance in pre-analytics, diagnostics, basic research and pharmaceutical drug discovery. The company operates in the market via the two business units Preanalytics and BioScience and has more than 2300 employees and 28 subsidiaries.
Established in Singapore in 2022, Greiner Bio-One Singapore serves as a regional hub supporting market development and customers across the Asia and Pacific regions. Greiner Bio-One Singapore is located at 112 Robinson Road, Singapore, and works closely with colleagues, customers, distributors and regional stakeholders across the APAC market.

Why join Greiner Bio-One Singapore?
You will have the opportunity to work in a regional APAC role within a global medical technology organisation, collaborating with colleagues across different markets and functions. The position provides exposure to regulatory and quality requirements across Asia-Pacific while contributing to products and solutions that support healthcare professionals, laboratories and patient safety.

We provide equal opportunities for everyone and see diversity as our strength. Therefore, we welcome all applicants – regardless of identifying characteristics such as gender, age, background, social status, veteran status, sexual orientation, religion, or mental and physical abilities. We have additionally set the goal of empowering women and increasing female leader representation. We foster an inclusive work environment and encourage all individuals to apply.

Job ID: 4487

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