Senior Quality Engineer

About CooperSurgical

CooperSurgical is a leading fertility and womens healthcare company dedicated to putting time on the side of women babies and families at the healthcare moments that matter most in life. As a division of CooperCompanies were driven by a unified purpose to enable patients to experience lifes beautiful moments. Guided by our shared values dedicated innovative friendly partners and do the right thing our offerings support patients throughout their lifetimes from contraception to fertility and birth solutions to womens and family care and beyond. We currently offer over 600 clinically relevant medical devices to healthcare providers including testing and treatment options as well as an innovative suite of assisted reproductive technology and genomic testing solutions. Learn more at.

Work location: North Tonawanda NY (on-site)

Scope:

The Quality Engineer Sr is responsible for owning the Change Control program and providing QA oversight of validation equipment lifecycle management and risk management systems. This role ensures compliance with FDA regulations and current Good Manufacturing Practices (cGMP) including 21 CFR Parts 210 211 applicable elements of 21 CFR Part 820 and relevant ISO standards (e.g. ISO 13485) while embedding risk-based thinking across all quality system processes and site operations and leads the application of formal risk management principles across the Quality Management System (QMS) ensuring business decisions process improvements and quality actions are prioritized justified and executed based on scientific data-driven risk assessment.

Job Summary:

The Quality Engineer Sr provides site-wide leadership in risk-based quality engineering with primary accountability for the Change Control program QA oversight of validation and equipment management and the integration of risk management into all quality and operational processes at the North Tonawanda NY facility. This role ensures that all changes validation activities and quality systems are executed using robust risk assessment methodologies enabling compliant efficient and inspection-ready operations and works extensively with cross-functional teams to support new and improved processes ensuring that risks are proactively identified evaluated controlled and continuously monitored. This role also leads and supports supplier quality investigations CAPA audit response and inspection readiness while contributing to site training and quality culture development.

• Own and govern the site Change Control program ensuring all changes are initiated risk-assessed approved implemented and closed in compliance with regulatory and internal requirements; drive continuous improvement in effectiveness cycle time and compliance metrics.
• Lead and embed risk management practices across the site applying ICH Q9 principles to Change Control validation investigations CAPA and supplier quality; facilitate formal risk assessments (e.g. FMEA) ensure risk-based decision-making and proactively identify and mitigate systemic risks.
• Provide QA oversight for validation and equipment lifecycle management including equipment qualification (IQ/OQ/PQ) process validation cleaning validation and CSV; ensure all activities are risk-based compliant and aligned with cGMP and data integrity requirements.
• Partner cross-functionally with Engineering Manufacturing Validation Regulatory Supply Chain and other stakeholders to support new and improved processes ensuring quality-by-design and risk-based principles are embedded in process design changes and technology transfers.
• Perform complex investigations and CAPA ensuring robust root cause analysis risk prioritization and implementation of effective sustainable corrective and preventive actions that address systemic issues.
• Support the site supplier quality program including supplier-related investigations CAPA change evaluations risk assessments and audit follow-up activities to ensure supplier compliance and performance.
• Support audit and inspection activities including internal supplier and regulatory audits; serve as a key QA representative during inspections ensure effective response to audit observations and maintain a continuous state of inspection readiness.
• Review and approve complex quality documentation ensuring accuracy completeness and compliance with cGMP and data integrity standards.
• Support site training initiatives and quality culture development including training on Change Control validation and risk-based quality systems; provide mentorship and technical guidance to cross-functional teams.
• Serve as site SME for Change Control validation oversight equipment quality systems and risk management influencing quality strategy and decision-making at all levels.
• Perform other duties as assigned.

Travel:

This position may require 10-20% domestic and/or international travel.

Knowledge Skills and Abilities:

• Advanced expertise in risk management methodologies (e.g. FMEA hazard analysis risk ranking tools) and their application in regulated environments.
• Strong experience applying ICH Q9 risk management principles within a pharmaceutical or medical device QMS.
• Proven ability to lead risk-based decision making across multiple quality systems.
• Advanced knowledge of Change Control ownership and governance.
• Deep understanding of validation and equipment lifecycle risk management.
• Extensive experience in investigations CAPA and root cause analysis with risk prioritization.
• Experience supporting or leading regulatory inspections and audit responses.
• Strong understanding of FDA (21 CFR 210/211/820) and ISO standards (ISO 13485).
• Ability to influence cross-functional stakeholders using data-driven risk insights.
• Excellent analytical communication and leadership skills.
• Ability to operate as the senior QA engineering authority onsite.

Work Environment:

• Production/Clean Room/Warehouse/Office Environment which may require long periods of sitting standing or getting up and down throughout the day.
• Occasionally lift to 35 pounds.

Experience:

• 5 years experience working in regulated manufacturing environment preferably within pharmaceutical or medical device related field.
• Significant experience leading risk-based quality systems Change Control and validation oversight.
• Demonstrated role as a senior or lead QA professional.

Education:

• Bachelors degree in a Health Engineering or Science field or associatesdegreewith 5 years of relevantexperienceor high school diploma with10 years of relevant experience required.
• Advanced degree preferred.

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Our Benefits:

As an employee of CooperSurgical youll receive an outstanding total compensation plan. As we believe your compensation goes beyond your paycheck we offer a great compensation package medical coverage 401(k) parental leave fertility benefits paid time off for vacation personal sick and holidays and multiple other perks and benefits. Please visit us atto learn more about CooperSurgical and the benefits of becoming a member of our team.

To all agencies: Please no phone calls or emails to any employee of CooperSurgical about this opening. All resumes submitted by search firms/employment agencies to any employee at CooperSurgical via-email the internet or in any form and/or method will be deemed the sole property of CooperSurgical unless such search firms/employment agencies were engaged by CooperSurgical for this position and a valid agreement with CooperSurgical is in the event a candidate who was submitted outside of the CooperSurgical agency engagement process is hired no fee or payment of any kind will be paid.

We are committed to equal employment opportunity regardless of race color ancestry religion sex national origin sexual orientation age citizenship marital status disability gender gender identity or expression or veteran status. We are proud to be an equal opportunity workplace.

For U.S. locations that require disclosure of compensation the starting base payfor this role is between$90000.00 - $115000.00 annually. Theactual base payincludes many factors and is subject to change and modification in the future. This position may also be eligible for other types of compensation and benefits.