Project Manager (INTL - Mexico)

Insight Global is seeking a Project Manager to support our Medical Device client. This consultant will sit remotely in Mexico and should have experience in a medical device environment, ideally supporting Quality Systems–related initiatives. This role will manage multiple, overlapping projects and work closely with senior stakeholders to drive execution and visibility. Day to day will consist of the following:

Responsibilities
-Manage multiple concurrent projects within a regulated medical device environment
-Coordinate and communicate with senior‑level stakeholders across teams
-Develop and maintain project plans, timelines, and status updates
-Prepare and coordinate slides, decks, and executive‑ready presentations
-Track risks, dependencies, and deliverables across initiatives

Compensation:
$16/hr to $20/hr.
Exact compensation may vary based on several factors, including skills, experience, and education

We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

-6-8+ years of project management experience within a medical device or regulated life sciences company
-Exposure to Quality Systems initiatives or programs
-Strong stakeholder management and communication skills
-Ability to manage competing priorities in a fast‑paced environment
-Ability to manage training workflows and documentation in a regulated environment.
-Excellent attention to detail, organizational skills, and ability to meet strict deadlines.
-Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).

-Experience with ComplianceWire is a plus, not required

-Prior experience in medical device or pharmaceutical industry.
-Familiarity with Windchill or other document management systems.
-Experience supporting audit remediation projects (FDA, EU MDR, etc.).
-Knowledge of Good Documentation Practices (GDP).

Benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.