QA Director

Scilligence; Massachusetts; Remote; USD 90,000 - 150,000; Full time

Job summary

Join a forward-thinking company as a QA Director in Massachusetts, where you will lead a dedicated QA team focused on optimizing quality assurance processes. This role involves managing software testing strategies, ensuring compliance with industry standards, and maintaining rigorous documentation for audits. You will thrive in a collaborative environment, working alongside talented professionals who are committed to excellence in scientific software. If you're passionate about quality assurance and eager to make an impact, this is the perfect opportunity for you to shine.

Qualifications

• 5+ years of QA management experience in enterprise software.
• Extensive knowledge of QA best practices and methodologies.

Responsibilities

• Lead and manage the QA team to optimize processes.
• Maintain documentation for auditing and compliance.

Skills

Quality Assurance Management

Software Testing

QMS or Document Management Software

ISO Regulations Knowledge

Time Management

Collaboration Skills

Education

Bachelor's or Master's in Chemistry, Biology, Pharmaceutical

Tools

Test Planning Tools

Documentation Software

Job description

We are looking for a QA Director to join our Cambridge team in Massachusetts. The primary role of this position is to lead our QA team and optimize our QA processes.

Responsibilities:

• Manage and lead QA team (remote)
• Optimize our QA strategy that aligns with the company's goals and objectives.
• Optimize our software testing process, including test planning, test case design, execution, and reporting.
• Maintain comprehensive documentation of testing processes, test plans, and test results for auditing and compliance purposes.
• Lead efforts associated with external audits against ISO regulations and standards

Ideal Qualifications:

• Bachelor's or Master's degree in Chemistry, Biology, Pharmaceutical or a related field.
• 5+ years of experience in a QA management role for enterprise software
• 3+ years experience with QMS or Document management software and industry standards
• Extensive experience in quality assurance and software testing, particularly in a scientific software environment.
• In-depth knowledge of software development methodologies and QA best practices.
• Knowledge of relevant industry regulations and standards (e.g., FDA CFR Part 11, ISO9001 and ISO27001).

Who You Are:

• Have initiative to learn whatever is needed in order to complete your task
• Highly organized, and results-focused, with excellent written and verbal (presentation) skills
• Excellent at time management and Able to prioritize tasks and detail-oriented
• Self-motivated and people-oriented, with the ability to work collaboratively and productively in a global, multi-cultural environment
• Creative in inspiring customer loyalty, solving problems and contributing to best practices

Job Type:Full Time

Job Location:MA