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Manager Microsoft Internal Audit Jobs in Puerto Rico

PR · On-site

Support internal audits and regulatory inspections as the Subject Matter Expert (SME) for Cleaning ... Ability to manage multiple validation projects simultaneously. * Strong attention to detail and ...

PR · On-site

Support internal audits and regulatory inspections as the Subject Matter Expert (SME) for Cleaning ... Ability to manage multiple validation projects simultaneously. * Strong attention to detail and ...

PR · On-site

Support internal audits and regulatory inspections as the Subject Matter Expert (SME) for Cleaning ... Ability to manage multiple validation projects simultaneously. * Strong attention to detail and ...

PR · On-site

Support internal audits and regulatory inspections as the Subject Matter Expert (SME) for Cleaning ... Ability to manage multiple validation projects simultaneously. * Strong attention to detail and ...

PR · On-site

... and internal audits.Ensure effective communication with clients at all times, including periodic ... Proficiency in Microsoft Windows applications: Word, Excel, Outlook, Canva Pro, Meta Business Suite ...

PR · On-site

Provides the tracking and improvement of internal control procedures based on system analysis ... Communicate audit results, consequences, and recommendations to operating management and assist in ...

PR · On-site

Works with the Benefit team, Account Management and Quality Internal Audits to evaluate complex ... Proficiency in Microsoft Office. * Possess a high degree of initiative, judgment, discretion, and ...

PR · On-site

... management, reporting requirements, and audit readiness. * Conduct periodic internal reviews or ... Proficiency in Microsoft Office 365 (Word, PowerPoint, Excel, etc.) * Computer knowledge * Business ...

Quality Engineer

Caguas, PR

$70K - $90K/yr

Plan and manage all process validation projects and customers related PPAP, FAI, V&V, DVT projects ... Participate in internal audits, customer audits, supplier audits, and regulatory Audits. Support ...

Quality Engineer

Caguas, PR · On-site

$62K - $68K/yr

Plan and manage all process validation projects and customers related PPAP, FAI, V&V, DVT projects ... Participate in internal audits, customer audits, supplier audits, and regulatory Audits. Support ...

Showing results 21-40

Manager Microsoft Internal Audit information

What is the difference between Manager Microsoft Internal Audit vs Internal Auditor?

AspectManager Microsoft Internal AuditInternal Auditor
CertificationsCIA, CPA, CISA often preferredCIA, CPA, CISA common
Work EnvironmentCorporate, internal audit teams at MicrosoftVaries: corporate, consulting, or external firms
ResponsibilitiesOversees audit processes, manages teams, strategic planningConducts audits, tests controls, reports findings
Industry UsageCommon in large tech companies like MicrosoftWidespread across industries and companies

The main difference is that a Manager Microsoft Internal Audit typically oversees audit teams and strategic processes within Microsoft, requiring leadership skills and advanced certifications. An Internal Auditor performs the hands-on testing and reporting of controls, often with less managerial responsibility. Both roles require similar certifications and work environments, but the manager role involves higher-level oversight and team management.

What are the most commonly searched types of Microsoft Internal Audit jobs in Puerto Rico?

The most popular types of Microsoft Internal Audit jobs in Puerto Rico are:

What are popular job titles related to Manager Microsoft Internal Audit jobs in Puerto Rico?

For Manager Microsoft Internal Audit jobs in Puerto Rico, the most frequently searched job titles are:

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What cities in Puerto Rico are hiring for Manager Microsoft Internal Audit jobs?

Cities in Puerto Rico with the most Manager Microsoft Internal Audit job openings:

Packaging Project Manager

Mirus Consulting Group

Gurabo, PR

Full-time

Re-posted 21 days ago


Job description

mîrus Consulting Group is a Puerto Rico based technical services firm headquartered in Humacao. The company specializes in Computer System Validation (CSV) and Information Technology consulting for the pharmaceutical and life sciences industries across Puerto Rico and parts of the United States. Its services include the assessment and validation of automation systems, network infrastructures, and business processes, as well as comprehensive project management support to ensure compliance, efficiency, and operational excellence.Key Responsibilities
  • Lead end-to-end execution of packaging-related projects, including planning, scheduling, budgeting, coordination, and implementation.

  • Coordinate activities across Packaging Operations, Engineering, Validation (CSV/CQV), Automation, Manufacturing, and Facilities to ensure successful project execution.

  • Manage packaging equipment installation, upgrades, modifications, integration, and startup activities.

  • Develop and maintain detailed project plans, schedules, resource plans, and risk mitigation strategies for packaging initiatives.

  • Ensure compliance with cGMP regulations, safety requirements, internal procedures, and quality standards throughout all project phases.

  • Oversee commissioning, qualification, and validation activities (IQ/OQ/PQ) associated with packaging equipment and systems.

  • Coordinate change control activities, impact assessments, technical documentation, and implementation plans.

  • Support packaging process improvements, operational readiness activities, and efficiency initiatives.

  • Serve as the primary point of contact between clients, vendors, contractors, and cross-functional internal teams.

  • Monitor project performance, budgets, deliverables, and KPIs while providing regular project status updates to leadership.

  • Identify and resolve project risks, operational challenges, scheduling conflicts, and resource constraints.

  • Support audits, inspections, and maintain projects in a state of compliance and inspection readiness.

Minimum Qualifications
  • Bachelor’s Degree in Engineering (Mechanical, Electrical, Chemical, Industrial, or related discipline required).

  • Minimum of 5+ years of project management experience within pharmaceutical, biotechnology, or medical device industries.

  • Proven experience supporting packaging operations, packaging equipment, serialization, labeling systems, inspection systems, or manufacturing support projects.

  • Strong knowledge of cGMP regulations and pharmaceutical packaging operations.

  • Hands-on experience with Commissioning, Qualification, and Validation (CQV) activities related to packaging systems and equipment.

  • Experience managing Change Control systems within regulated manufacturing environments.

  • Experience coordinating vendors, contractors, packaging equipment manufacturers, and cross-functional project teams.

  • Strong leadership, organizational, communication, and problem-solving skills.

  • Bilingual communication skills (English and Spanish preferred).

  • Proficiency in MS Office applications including Word, Excel, PowerPoint, and Microsoft Project.

This Company is an equal employment opportunity employer. We adhere to a policy of making employment decisions without regard to race, color, religion, sex, sexual orientation, national origin, citizenship, age or disability. We assure you that your opportunity for employment with this Company depends solely on your qualifications.