Job summary
Job overview
The Manager, Quality Assurance at Standard BioTools will lead the quality team in enhancing the Quality Management System and ensuring compliance with quality standards across various international markets.
Responsibilities and impact
Daily responsibilities include managing the quality system, leading quality operations for lab and design controls, overseeing CAPA processes, and mentoring team members to foster engagement and growth.
Experience and skills
Candidates should have a Sc./M.Sc. in Physical Sciences, Engineering, or Biology, along with 5+ years in a quality function, preferably in In Vitro Diagnostics, and experience with ISO standards and quality management systems.
Work environment and culture
The work environment is a typical office setting with occasional laboratory work, requiring on-site presence at least three days a week and some international travel.
Company information
Standard BioTools is focused on developing tools to accelerate breakthroughs in human health, supporting a range of regulatory and quality requirements across multiple markets.
Job location and travel
The position is based in Boulder, requiring on-site work and some travel.
Company overview
Standard BioTools, formerly known as Fluidigm, specializes in developing and manufacturing innovative life science research tools and systems. They generate revenue by selling advanced instruments, reagents, and software used in genomics, proteomics, and cell biology research. Founded in 1999, the company has a rich history of pioneering microfluidic technologies and has undergone significant rebranding to align with its expanded focus on comprehensive biological research solutions.
How to land this job
Tailor your resume to emphasize your leadership experience in quality assurance and management of quality systems, particularly in laboratory, pharma, or medical device environments, as these are crucial for the Manager, Quality Assurance role at Standard BioTools.
Highlight your knowledge and experience with ISO 9001:2015, ISO 13485:2016, 21 CFR Part 820, and CLIA regulations, as well as your ability to implement and maintain quality management systems, as these are key requirements in the job description.
Apply through various platforms including Standard BioTools' corporate site, LinkedIn, and any other relevant job boards to maximize your chances of being noticed for this position.
Connect with professionals in the quality assurance division at Standard BioTools on LinkedIn. Ice breakers could include discussing your shared interests in quality standards or asking about their experiences with implementing ISO certifications.
Optimize your resume for ATS by incorporating specific keywords from the job description such as 'Quality Management System', 'ISO 9001', 'CAPA', and 'design controls' to ensure it passes initial screenings.
Utilize Jennie Johnson's Power Apply feature to streamline your application process, ensuring your resume is tailored and effectively highlights your qualifications while managing your time efficiently during your job search.
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