Assoc II, Quality

Baxter Healthcare - Welch Allyn de Mexico, S. de R.L. de C.V.; Tijuana; Presencial; MXN 200,000 - 400,000; Jornada completa

Descripción de la vacante

A medical technology company in Tijuana seeks an Associate II, Quality who will lead multi-functional teams as an Owner of Field Interventions. Responsibilities include handling Field Actions to closure, leading departmental activities, and collaborating with internal customers. The ideal candidate will hold a Bachelor's degree in sciences or engineering, have 3-5 years of relevant experience in a Medical Device or Pharma company, and possess strong critical thinking and problem-solving skills. Proficiency in English (B2+) is required.

Formación

• 3-5 years of experience in Quality with a Medical Device/Pharma company or similar industry.
• B2+ English proficiency required.
• Ability to invent new methods for analyzing large data.

Responsabilidades

• Lead multi-functional teams as an Owner of Field Interventions.
• Handle Field Actions (FAs) and oversee their closure.
• Participate in FA review boards and prepare monthly status reports.

Conocimientos

Critical thinking

Problem solving

Collaboration

Detail oriented

Educación

Bachelor’s degree in sciences or engineering

Descripción del empleo

Your role at Baxter:

As Assoc II, Quality, you will lead multi-functional teams as an Owner of Field Interventions. You will facilitate the execution and closure of multiple US/global Field Actions. This position supports additional field action process activities as detailed below

What you'll be doing:

• Responsible for handling Field Actions (FAs) as FA Owner through FA closure.
• Lead daily departmental activities for areas of direct responsibility
• Lead activities of self and Field Action (FA) team members in achieving defined Quality/FA goals in an efficient, accurate, and timely manner. Must be recognized as an authority in their area and demonstrate leadership ability
• Participate in FA review boards and Monthly reviews when vital, coordinate approvals for FA related documents, and drive FAs to closure per approved plans
• Lead FA Strategy team meetings to draft customer letters and Global FA Plans with global multi-functional teams
• Collaborate with internal customers on issues and questions related to the implementation of FAs
• Prepare and Verify FA monthly status reports
• Assist with data collection and report generation
• Perform periodic reviews for FA communications and coordinate efforts with other FA staff to ensure accurate documentation and data is assembled, entered and stored appropriately
• Work closely with regional gatekeepers, business leads, and FA team members to implement and support FA plans, supervise FA completion and resolve issues to drive FA’s to closure
• Present FA Metrics to management on an as needed basis and participate in internal and external inspections and assist with implementing solutions to audit findings
• Be directly involved in, and where appropriate, lead improvement projects which may include improving current FA processes, data generation, report development and presentation, or improving other quality processes /systems to demonstrate lean proficiencies
• Prepares periodic metrics for executive and segment management reviews, as needed

What You'll Bring!

• Bachelor’s degree in sciences or engineering.
• 3-5 years of experience in Quality with a Medical Device/Pharma company or other similarly supervised industry.
• B2+ English.
• Understanding of scientific strategies and ability to invent new methods or new avenues of analyzing large data.
• Strong critical thinking and problem solving skills.
• Detail Oriented.
• Collaboration and Teamwork