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COPY - Project Manager (INTL - Mexico)

Insight Global

Danvers, MARemoteJob$16–20/hrPosted 1mo agoSeen in employer's feed 5 days ago

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At a glance

Compensation
$16–20/hr
Location
Danvers, MARemote
Work Authorization
Not specified

Job overview

Insight Global is hiring a COPY - Project Manager (INTL - Mexico). Insight Global is seeking a Project Manager to support a medical device client. This consultant will work remotely from Mexico, ideally with experience in Quality Systems-related initiatives within a medical device environment. The role involves managing multiple projects, coordinating with senior stakeholders, and driving execution and visibility.

Key focus areas include Manage multiple concurrent projects within a regulated medical device environment, Coordinate and communicate with senior-level stakeholders across teams, and Develop and maintain project plans, timelines, and status updates.

Successful candidates bring Project Management Experience, Quality Systems Exposure, and Audit Remediation Experience. Important skills include Quality Systems Initiatives, Stakeholder Management, Communication, Managing Competing Priorities, Managing Training Workflows, and Documentation.

Skills & qualifications

RequiredNice to have

Skills

Quality Systems InitiativesStakeholder ManagementCommunicationManaging Competing PrioritiesManaging Training WorkflowsDocumentationAttention to DetailOrganizational SkillsMeet Strict DeadlinesMicrosoft Office SuiteExcelMicrosoft WordPowerPointComplianceWireWindchillDocument Management SystemsSupporting Audit Remediation ProjectsFDAEU MDR

Qualifications

6-8+ Years Project Management ExperienceMedical Device Environment ExperienceRegulated Life Sciences Company ExperiencePrior Medical Device Industry ExperiencePrior Pharmaceutical Industry Experience

Full job description

Job Description

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 [email protected] 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/.

Skills and Requirements

-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).

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