Life Science Job at Masimo | Candidates Apply Now
Are you looking for a Life Science Job in Regulatory Affairs and Quality Assurance? Masimo Careers is hiring for the position of Quality Regulatory Operations Specialist in Bengaluru, India. This is an excellent opportunity for life science graduates and professionals with experience in regulatory affairs, quality assurance, and medical devices to build a rewarding career. If you’re searching for QC Jobs, Life Science Jobs, or the latest Masimo Careers, explore the complete job details below and apply online.
About Masimo
Masimo is a global medical technology company recognised for developing innovative patient monitoring technologies, sensors, and healthcare solutions. The company focuses on improving patient outcomes through advanced, non-invasive monitoring systems and serves hospitals and healthcare providers across the world. Through Masimo Careers, professionals have the opportunity to work on impactful healthcare innovations while advancing their careers in regulatory affairs, quality assurance, and life sciences.
Job Information
- Company: Masimo
- Position: Quality Regulatory Operations Specialist
- Job ID: 3830
- Location: Bengaluru, India
- Department: Regulatory Affairs
- Job Schedule: Full-Time
Key Responsibilities
The selected candidate will be responsible for:
- Support RA/QA operations across JPAC, including maintaining compliance and documentation accuracy.
- Assist with tender support activities, including preparation and review of regulatory and quality documentation.
- Collaborate with Commercial and cross-functional teams to support the timely submission of required documentation.
- Support regulatory intelligence activities, including tracking regulatory updates and assisting with impact assessments.
- Maintain and organise regulatory documentation and records in alignment with internal systems and requirements.
- Assist in Quality Management System (QMS) processes (ISO 13485), including CAPA tracking, change control, and audit preparation.
- Support internal and external audits, including documentation collection and coordination.
- Assist with complaint handling, vigilance, and post-market activities, including data tracking and documentation.
- Provide support for field actions and recalls, ensuring documentation and coordination activities are maintained.
- Assist with distributor/importer registrations and compliance activities across JPAC markets.
- Support labelling and claims review activities, ensuring documentation is compliant with regional requirements.
- Utilise regulatory and quality systems (RIM/eQMS) to maintain accurate records and support reporting.
- Contribute to process improvements and standardisation initiatives.
Qualifications
Candidates should possess:
- Bachelor’s degree in Life Sciences, Pharmacy, Biomedical Engineering, or a related field.
Experience
Applicants should have:
- 2–5 years of experience in Regulatory Affairs and/or Quality Assurance (medical device or healthcare preferred).
- Basic understanding of JPAC regulatory frameworks (e.g., CDSCO, PMDA, TGA, HSA, NMPA).
- Exposure to Quality Management Systems (ISO 13485) and related processes (CAPA, audits, change control).
- Exposure to or interest in regulatory submissions and product lifecycle processes.
Skills Needed
The ideal candidate should have:
- Strong attention to detail and organisational skills.
- Good analytical and problem-solving abilities.
- Strong written and verbal communication skills.
- Ability to work effectively in a cross-functional environment.
- Familiarity with document management or regulatory systems (RIM/eQMS) is a plus.
If you’re searching for a Life Science Job, QC Jobs, or the latest opportunities through Masimo Careers, this Quality Regulatory Operations Specialist position in Bengaluru is an excellent opportunity to grow your career in Regulatory Affairs and Quality Assurance. Review the eligibility criteria carefully and apply online to become a part of Masimo’s innovative healthcare team.
