Quality Associate

Baxter Healthcare; Tijuana; Presencial; MXN 839,000 - 1,120,000; Jornada completa

Descripción de la vacante

A healthcare company in Tijuana seeks a Compliance Quality Associate to ensure the regulatory compliance of complaint records. Ideal candidates will have a degree in Science or Engineering and 2-5 years of experience in a cGMP environment. Responsibilities include complaint handling, regulatory reporting, and continuous improvement efforts. Applicants should demonstrate strong critical thinking and leadership skills in a collaborative setting.

Formación

• 2-5 years relevant work experience in cGMP related industry.
• Experience with driving process improvement initiatives preferred.
• Ability to communicate across different functions.

Responsabilidades

• Serve as a Subject Matter Expert for complaint handling.
• Establish and maintain processes to ensure compliance.
• Monitor automated tools for accuracy within complaint records.

Conocimientos

Ability to handle multiple projects

Problem solving

Leadership

Strong critical thinking

Detail Oriented

Educación

Bachelor’s degree in Science or Engineering

Herramientas

Complaint management system

Automated tools for compliance

Descripción del empleo

This is whereyour work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride.

This is where your work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride.

Your Role at Baxter

The Compliance Quality Associate is responsible for identifying, assessing, and driving actions to correct regulatory and quality risks within complaint records, to ensure compliance and congruency of complaint records across Regions and Segments. This position serves as a Subject Matter Expert for Postmarket surveillance processes such as complaint handling and Regulatory Reporting. This role is also responsible for process and tools needed to ensure compliance and for driving actions/corrections to the complaint records.

Ability to handle multiple projects and demonstrate effectiveness in task completion, decision-making, empowerment of others, problem solving and leadership. A strong understanding of the complaint management system, procedures, FDA, ISO and Baxter Quality systems is also required.

Your Team at Baxter

Within Quality, every role makes a difference. Products that Baxter makes are shipped worldwide for patients in need. Whether it's building a new process from scratch or facing a never-before-seen production hurdle, individuals within Quality are given the trust and opportunity to bring creativity to the table. Regardless of your specific role with a product, it is sure to touch a portion of our global operation.

The mission of Baxter is to save and sustain lives. This mission is embedded into everything we do. This means if there is a decision to be made where quantity and quality are at odds, we will always choose quality. Our patients come first, always.

The Quality function values both working together as a team and independently. We draw energy from working in a plant or an office where there are opportunities to collaborate. As the company evolves, so does the way our team approaches work as it strives to create top-of-the-line products.

We build relationships with each other to get work done. Building these relationships is easy because we all share common traits of being reliable, ethical, and caring. We lean on our colleagues for their expertise and hold each other accountable. We feel empowered to speak up when there's a new insight or opportunity to improve something. This open dialog builds trust within the team and helps create a better product for our customers.

What you'll be doing

• Serves as a Subject Matter Expert for complaint handling and Regulatory Reporting
• Establishing and maintaining processes and automation tools to ensure compliance and congruence of complaint records
• Monitoring output of the automated tools and proactively identifying potential congruency or accuracy issues within complaint records
• Ensuring corrections are made in a timely manner and monitoring results of the corrections and actions
• Effectively identifying improvements and leading continuous improvement efforts and projects, including NCRs/CAPAs
• Leading audit readiness activities and efforts for Postmarket Surveillance function, including potential risk identification, mitigations, and improvements
• Participating in external and internal Audits as a complaint process Subject Matter Expert, including direct interactions with the Auditor(s), providing support to Audit requests, providing support to responses, and driving completion of Audit commitments
• Maintaining a high level of expertise in current regulatory requirements
• Writing, reviewing, and revising written Procedures and submitting procedural changes as needed
• Creating operations metrics/KPI performance data and leading complaint timeliness governance as assigned
• Coaching complaint handling team on complaint file documentation, congruency and accuracy
• Providing training of the Product Surveillance team.
• May perform other Postmarket activities as assigned

What you'll bring

• Bachelor’s degree in Science or Engineering required
• 2-5 years relevant work experience in cGMP related industry
• Experience with driving process improvement initiatives and projects preferred
• Ability to effectively communicate (verbal and written) across different functions and across multiple levels within the organization
• Strong understanding of complaint process and regulatory reporting regulations applicable to Baxter products (medical devices, pharmaceuticals, etc.)
• Strong critical thinking and problem solving skills
• Ability to work independently and to prioritize effectively
• Ability to drive decisions and actions quickly and effectively
• Ability to make independent decisions
• Understanding of scientific strategies and ability to invent new methods or new avenues of analyzing large data
• Good project management skills
• Collaboration and Teamwork
• Detail Oriented
• Strong technical writing skills

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice

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Emilio Flores #2471-A|Col. Cañon del Padre|22203 Tijuana, BCN|Mexico