A Snapshot of Your Day as Quality Supervisor As a Quality Supervisor, your day is defined by a balance of strategic leadership and technical rigor, serving as the primary guardian of our product integrity and regulatory excellence. You will provide essential direction to the quality control team, fostering an environment where high performance meets uncompromising standards. Much of your time will be dedicated to developing and implementing sophisticated programs for testing and trend analysis, ensuring that every facet of our operation remains in strict alignment with Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP).

Whether you are spearheading ISO initiatives or driving facility-wide quality goals, your expertise ensures that our compliance framework is both robust and forward-thinking.

Beyond oversight, you are a master of execution and timing. You will spend your day planning staff strategies to guarantee that testing and releases are completed on schedule, taking personal responsibility for the evaluation and release of highly regulated, critical products. As a pillar of our Quality Management System (QMS), you will actively manage and provide vital inputs for core processes including design control, risk management, and corrective actions.

You serve as a key advisor to Management, translating complex process data into clear, actionable insights. By providing the rationale behind critical decisions—always prioritizing regulatory compliance—you ensure that our leadership team is fully informed and that our commitment to quality remains our competitive advantage.

How You Will Make an Impact Strategic Leadership: Lead and develop a high-performing QA specialist team, ensuring technical competency and resource allocation are aligned with both regulatory requirements and operational priorities.

Regulatory & Sanitary Alignment:



Act as a vital link to the Responsible Sanitary, ensuring all data-driven decisions, cold chain compliance, and stability programs are fully aligned and transparently communicated.

Operational Agility: Optimize quality control systems and continuous improvement initiatives to enhance process efficiency and commercial impact without disrupting business continuity.

Quality System Oversight: Manage the full lifecycle of quality processes, from reviewing engineering designs and change requests to overseeing IQ/OQ/PQ validation plans and maintaining the validated state.

Risk & Issue Resolution: Lead critical investigations and corrective actions (CAPA), ensuring rapid closure of quality issues and the precise execution of ship holds, FSCAs, or recalls.

Actionable Intelligence: Provide Management and the Responsible Sanitary with continuous, trend-based reporting to enable informed, joint decision-making and full visibility of process health.

Audit Readiness & Training: Drive a culture of compliance by coordinating cGMP/ISO training and leading internal and external audits to ensure the facility remains inspection-ready at all times.

What you brings Educational Foundation: A Bachelor’s degree (BA/BS) or equivalent in a science, engineering, or a related technical field.

Proven Leadership: 5+ years of relevant experience in Quality Systems, including a strong track record in a supervisory or people-management role.

Regulatory Expertise:



Deep experience operating within highly regulated environments, ensuring strict adherence to industry standards.

Risk Management Mastery: A solid understanding of risk management regulations and the ability to apply these principles to complex operational challenges.

Training Excellence: Proven experience acting as a GMP and/or ISO trainer, with the ability to build technical competencies and foster a culture of compliance across the team.

Compliance Mindset: A combination of education and hands-on experience that enables you to balance regulatory requirements with operational agility.

Compensation: Market compatible compensation.

Who We Are: For 70 years, Bio-Rad has focused on advancing the discovery process and transforming the fields of science and healthcare. As one of the top five life science companies, we are a integral leader in developing, manufacturing, and marketing a broad range of high-quality research and clinical diagnostic products. We help people everywhere live longer, healthier lives.

Recently voted a Best Place to Work, Bio-Rad offers a unique employee experience with collaborative teams that span the globe. Here, you are supported by leadership to build your career and are empowered to drive change that makes an impact you can see.

EEO Statement: Bio-Rad is an Equal Employment Opportunity/Affirmative Action employer, and we welcome candidates of all backgrounds. people with special abilities, and people of all races, ethnicities, genders, ages, and orientations are encouraged to apply.

Agency Non-Solicitation: Bio-Rad does not accept agency resumes, unless the agency has been authorized by a Bio-Rad Recruiting Representative. Please do not submit resumes unless authorized to do so. Bio-Rad will not pay for any fees related to unsolicited resumes.

📌 Supervisor de Aseguramiento de la Calidad (Cuautitlán Izcalli)
🏢 Bio-Rad LAM
📍 Cuautitlán Izcalli