5 дней назад
Software Quality Engineering Manager
153 216 - 239 400$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Software Quality Engineering Manager (Laboratory Software): Leading quality engineering teams that test and validate software powering analytical instruments, with an accent on automation, regulatory compliance, and risk-based verification. Focus on developing distributed teams, integrating quality throughout the product lifecycle, and ensuring traceability, test evidence, reliability, and compliance for chromatography and mass spectrometry software.
Location: US-CA-Santa Clara
Salary: $153,216–$239,400 per year, plus eligibility for bonus, stock, and benefits.
Company
advances scientific and laboratory work by delivering analytical instruments and software that provide trusted results.
What you will do
- Lead and develop Software Quality Control and Test Engineering teams in Santa Clara and Waldbronn.
- Set priorities, allocate resources, and build organizational capabilities aligned with business objectives.
- Coach engineers and technical leaders while supporting career development and evolving quality and regulatory needs.
- Partner with software development, product management, and regulatory teams to define verification and validation strategies.
- Oversee manual and automated testing, risk management, defect resolution, traceability, and test evidence.
- Drive test automation, shift-left quality, continuous improvement, and compliance with applicable QMS and regulatory requirements.
Requirements
- Bachelor’s or Master’s degree in Life Sciences, Analytical Chemistry, Software Engineering, Computer Science, or a related field.
- At least one year of formal or informal leadership experience involving people, projects, or programs.
- Experience leading software quality or testing organizations covering both manual and automated testing.
- Knowledge of chromatography and mass spectrometry software, including acquisition, instrument control, data processing, and workflow solutions.
- Knowledge of ISO 9001, FDA 21 CFR Part 11, ALCOA+ data integrity principles, Agile/Scrum, CI/CD, Secure SDLC, and risk-based testing.
- Strong stakeholder management, communication, and presentation skills across engineering, product, regulatory, and business functions.
Nice to have
- Experience managing third-party suppliers or outsourced development and testing partners.
- Experience managing geographically distributed teams across regions and time zones.
- Experience leading organizational change and strategic initiatives in a global environment.
- Understanding of analytical laboratory workflows and LC and LC/MS acquisition software requirements.
Culture & Benefits
- Full-time day-shift position with no stated end date.
- Occasional travel is required.
- Benefits include bonus eligibility, stock, and company benefits.
- Inclusive workplace committed to equal employment opportunity and accessibility.
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