QA Software Manager
- Employer
- Thornshaw Recruitment
- Location
- Dublin (County), Leinster (IE)
- Salary
- Negotiable depending on experience
- Start date
- 31 Aug 2022
- Closing date
- 30 Sep 2022
View more
- Discipline
- Quality, QA / QC
- Hours
- Full Time
- Contract Type
- Contract
- Experience Level
- Management
Job Details
On behalf of my client, we have a new vacancy for a Software QA Manager. Innovation & Research, this is a fantastic time to join a cutting-edge medical device company.
Role & Responsibilities:
To manage quality and compliance activities associated with Software and drive the execution of related objectives
- Lead and manage software quality assurance activities and drive the execution of day-to-day QMS activities towards related objectives Drive software quality assurance improvements, as needed, to ensure that all software quality systems remain fit for purpose and satisfy all customer requirements Develop quality and regulatory strategies for company software, data management, and cybersecurity with QA/RA Director and Technical Team Collaborate with the wider team to ensure that necessary and sufficient QA activities are planned, executed, and recorded Interpret relevant standards and regulations and ensure the company meets requirements ahead of regulatory submissions and audits Participate in cross functional product development and provide practical QA and Design Assurance expertise, related to software design and development, risk management, manufacture, and control Manage suppliers to support quality assurance of product software and assessment/validation of QMS software Train and mentor members of the QA/RA Team and Technical Team with a focus on Software Quality and Compliance best practices
Engage with the QMS and the organisation to ensure delivery of the overall quality strategy & support the achievement of the business quality objectives
Essential
- Bachelor’s Degree in Engineering, Science, or related field
- 7+ years’ experience in medical device quality/design assurance role with focus on medical device software Recent regulatory experience including FDA regulations, ISO 13485, Medical Device Directive and other applicable national and international regulations and standards Desirable
- Master’s degree in Engineering, Science, or related field
- Experience in medical device software design, development, and control
Experience with, or exposure to medical electronics development
For full job spec and details send your CV to zhamilton@thornshaw.com or call Zoe at +353 1 2784671
Thornshaw Scientific is a division of the CPL Group www.thornshaw.com
Company
Thornshaw Scientific Recruitment was first established in 1999 and since then has become a leader in Scientific recruitment. In 2005 we partnered with Cpl Resources, one of Europe’s most successful recruitment companies.
Our wealth of experience in specialised recruitment allows us to offer the right solution to each employer, whatever their recruitment requirements.
Over the years we have developed strong relationships with our clients in the market and we pride ourselves on our repeat business from clients.
Our Industries
We are a global provider and have been providing a reputable recruitment service to the Biotech, Pharmaceutical, Clinical Research, Medical Device, Engineering and Healthcare industries for over 20 years.
Our Specialities
Clinical Research, Regulatory Affairs, Quality Assurance, Medical Affairs, Pharmacovigilance, Biostatistics, QC, Validation.
Our Mission
For further details on our services contact Tina at +353 1 2784701 or email tdunne@thornshaw.com
- Website
- http://www.thornshaw.com/
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