Human Resources Visa Sponsorship Jobs in New York

This is a highly visible, mission‑critical role that requires strong leadership, exceptional communication, and a deep understanding of quality systems in regulated environments. In this role you will be leading meetings, managing projects, escalating risk on time - leading remediation team for process validation - set up the governance structure and drive the change, creating the procedures.

Job Responsibilities

• Program Management: Manages multi-site or medium/high complex programs over 2–3 years or financial impact of > €10M. Innovates and elevates program and portfolio capabilities.
• Strategic Leadership: Provides strategy and direction for major functional areas through assessment of intangible variables and identification of fundamental issues.
• Risk Management: Encourages balanced risk-taking and mitigates risks to maintain program health. Familiarity with risk management standards such as ISO 14971.
• Quality Compliance: Utilizes quality principles (QMS, CAPA, Nonconformance, Calibration, PM, Process and Production Controls, Warehousing, etc.) within project management.
• Stakeholder Engagement: Interacts internally and externally with senior-level management; negotiates extremely critical matters including influencing policymaking.
• Methodology & Coaching: Expertise in applying PM standards (PMI, PMBoK, SAFe) and coaching others in project/program management processes.
• Operational Execution: Uses detailed knowledge of company operations to promote innovative concepts and develop resolutions to critical issues.
• On-site presence required.

Minimum Requirements

• Education: Bachelor’s or Master’s degree in life sciences, business administration, or engineering.
• Experience: 5–10 years of relevant working experience, including all aspects of project development and execution. 5+ years of program management experience with a demonstrated record of success.
• Certification: Philips Project Management Practitioner/Expert/Master or equivalent (PMI, PMBoK, SAFe).
• Compliance Knowledge: Knowledge of ISO 13485 and FDA 21 CFR Part 820 for medical devices; comprehensive training in Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP).

Preferred Qualifications

• Experience: Experience working in programs specifically supporting the program manager in program management activities.
• Expertise: Known authority on process-oriented skills with consistent application.

Preferred Skills

• Project/Program Management (PMI, PMBoK, SAFe)
• Quality Management Systems (QMS)
• CAPA Processes
• ISO 13485 & FDA 21 CFR Part 820
• ISO 14971 Risk Management
• Strategic Planning & Policy Influencing
• Negotiation & Senior Stakeholder Management
• Innovative Problem Solving

How We Work Together

We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations. For this project, you’ll be contracted via a Randstad company as a temporary worker/contractor and placed at our Client. As a contractor, you'll enjoy cutting-edge challenges and unexpected experiences that make you a more in-demand professional.

Equal Opportunity Employer

Randstad is an equal opportunities employer and does not discriminate against Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact kari.carapella@randstadsourceright.com