Work Flexibility: Hybrid or Onsite
What will you do:
- Primarily responsible for Risk management and risk assessment as per ISO 14971 Risk Table creation & Analysis FMEAs Quality Plan Literature Review Device Master Record Quality Training Plan and Technical File.
- Primary participant in new supplier selection validation and contract development. Assists vendors in resolving manufacturing and quality issues as required.
- Partners with the operations team to develop and maintain a robust internal and external supply chain.
- Develop procedures for incoming in-process and final inspections for new product development
- Assists/Leads in the trending and analysis of quality data (e.g. complaints scrap warranty return rate etc.) and provides guidance to address issues as appropriate.
- Authors and reviews procedures to ensure GMP and ISO 13485 compliance and provide inputs for NPDP for adherence to QMS along with good documentation practices
- Lead product quality related projects. Supports the business in addressing and solving quality problems
- Support process validation programs for new product development
- Work with engineering & manufacturing teams to develop robust verification test strategies to ensure product safety and reliability
What you need:
Basic Qualifications:
- Bachelors in mechanical or biomedical or Biotech Engineering.
- Good understanding of Quality Management Systems. (ISOCRF 820)
- Minimum 2 to 6 years of relevant work experience.
- Experience in the NPD process and various phases of new product development.
- Knowledge of ISO 14971 IEC -1 family of standards.
Preferred Qualifications:
- Good analytical and problem-solving skills.
- Demonstrated ability to effectively work with others in various coordinate disciplines and on multi-national teams.
- Expert-level knowledge of current industry standards for New Product Development and risk management practices
- Excellent communication and presentation skills
- Must have delivered multiple projects in AQE function and understand Risk Management processes in depth.
Travel Percentage: 20%
Work Flexibility: Hybrid or OnsiteWhat will you do:Primarily responsible for Risk management and risk assessment as per ISO 14971 Risk Table creation & Analysis FMEAs Quality Plan Literature Review Device Master Record Quality Training Plan and Technical File.Primary participant in new supplier sele...
Work Flexibility: Hybrid or Onsite
What will you do:
- Primarily responsible for Risk management and risk assessment as per ISO 14971 Risk Table creation & Analysis FMEAs Quality Plan Literature Review Device Master Record Quality Training Plan and Technical File.
- Primary participant in new supplier selection validation and contract development. Assists vendors in resolving manufacturing and quality issues as required.
- Partners with the operations team to develop and maintain a robust internal and external supply chain.
- Develop procedures for incoming in-process and final inspections for new product development
- Assists/Leads in the trending and analysis of quality data (e.g. complaints scrap warranty return rate etc.) and provides guidance to address issues as appropriate.
- Authors and reviews procedures to ensure GMP and ISO 13485 compliance and provide inputs for NPDP for adherence to QMS along with good documentation practices
- Lead product quality related projects. Supports the business in addressing and solving quality problems
- Support process validation programs for new product development
- Work with engineering & manufacturing teams to develop robust verification test strategies to ensure product safety and reliability
What you need:
Basic Qualifications:
- Bachelors in mechanical or biomedical or Biotech Engineering.
- Good understanding of Quality Management Systems. (ISOCRF 820)
- Minimum 2 to 6 years of relevant work experience.
- Experience in the NPD process and various phases of new product development.
- Knowledge of ISO 14971 IEC -1 family of standards.
Preferred Qualifications:
- Good analytical and problem-solving skills.
- Demonstrated ability to effectively work with others in various coordinate disciplines and on multi-national teams.
- Expert-level knowledge of current industry standards for New Product Development and risk management practices
- Excellent communication and presentation skills
- Must have delivered multiple projects in AQE function and understand Risk Management processes in depth.
Travel Percentage: 20%
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