Software Quality Engineer (Clinical Testing)

About Us

Revvity is a developer and provider of end-to-end solutions designed to help scientists, researchers, and clinicians solve the world's greatest health challenges. We pair the enthusiasm of an industry disruptor with the experience of a longtime leader. Our diverse team of 11,000+ colleagues from around the globe are vital to our success and the reason we're able to push boundaries in pursuit of better human health.

Find your future at Revvity

In this role, the Software Quality Engineer for the Revvity Omics Clinical Laboratories will provide support to Laboratory Directors, Bioinformatics, Information Technology (IT) and related personnel on software and data quality related matters. S/he will work with the Sr. Director, Quality Assurance to develop, implement, execute, and maintain policies and procedures as well as training and education programs, with an emphasis on software development, software implementation, and data related concerns such as security, storage and destruction. This role requires performing internal and external audits, as well as developing and maintaining required documentation and quality metrics. S/he will participate in quality meetings. A strong candidate for this position will be able to maintain good rapport and communication with leadership and team members while ensuring solid execution of quality programs.

Duties and Responsibilities:

• Provide advice and support to the Laboratory Directors, Bioinformatics, Information Technology (IT), Quality Manager and testing personnel on software and data quality issues

• Assist in the implementation of assurances, process controls, and CAPA systems designed to meet or exceed internal and external requirements with an emphasis on software and data related items

• Understand the Document Control System (PolicyTech) to ensure SOPs, Trainings and Policies are current versions and assigned appropriately. Notify Department leaders of employee signoffs not completed within deadlines

• Assist in the review of SOPs, validations, and incident reports with emphasis on software and data related items to ensure they meet Quality standards and adhere to company guidelines

• Participate in the maintenance of laboratory licensure as required by CLIA, CAP and other regulatory bodies

• Quality assurance and control of laboratory performance through internal and external audits

• Training & Education: Assist with training and education programs, to educate employees and management on quality processes, standards, and results

• Project Management: Participate in the planning, initiation, and management of quality improvement projects

• Lead and implement various product and process improvement methodologies

• Maintain good communication with leadership, team members and customers

• Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Data privacy and security, and other regulatory requirements

• Familiarity with operation of laboratory instruments and applicable computer software and data

• Other duties as assigned

Basic Qualifications:

• Bachelor of Computer Science or related degree

• Minimum 3 years of experience in clinical / healthcare quality management

• Demonstrated experience with Quality Assurance and Quality Control of software and data

Preferred Qualifications:

• Knowledge of clinical laboratory, clinical trial and / or life science manufacturing software and data requirements

• Experience with healthcare data privacy and protection requirements

• Able to partner and work collaboratively with laboratory operations staff

• Proven track record of delivering continual positive process improvement in systems and process

• Proven leadership and excellent organization and communication skills

• A good balance of negotiating and influencing skills

• Excellent presentation skills

• Be detail oriented, organized, with excellent verbal and written communication skills

• Able to work effectively and able to deliver on tight datelines

• Comfortable working in a fast-paced environment

Working Conditions: (describe office, lab environment, include shifts and any travel)

• This position on-site preferred with remote considered; must be able to work with computer, screen, and keyboard for majority of time

• A professional work environment that is private, free of distraction, and with limited background noise must be maintained.

• Video and voice calls are required

• Travel of 0 - 10% of time

Physical Requirements:

• While performing the duties of this job, the employee is regularly required to sit, stand, and use a keyboard, type

• Reach above/below the shoulder, bend at the knees and waist

What do we offer?

We provide competitive and comprehensive benefits to our employees.Below are some highlights of our benefits:

• Medical, Dental, and Vision Insurance Options

• Life and Disability Insurance

• Paid Time-Off

• Parental Benefits

• 401k with Company Match

• Employee Stock Purchase Plan

Learn more about Revvity's benefits by visiting ourWhy Revvitypage.

*For benefit-eligible roles only. Part-time and temporary roles may not be eligible for all benefits listed. Please reach out to your recruiter for more information.

Revvity is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability status, age, or veteran status or any other characteristics protected by applicable law. Revvity is committed to a culturally diverse workforce.