Project Manager

Acro Service Corp; San Clemente (CA); On-site; USD 80,000 - 120,000; Full time

Job summary

Acro Service Corp is looking for a Senior Project Manager to join their R&D team in San Clemente, California. This role involves leading complex projects in a regulated environment, supporting various business units including Infusion, Oncology, and Pain Management.

The ideal candidate will have over 4 years of project management experience, strong communication skills, and proficiency in MS Project and related tools. Experience in the medical device or healthcare sectors is preferred.

Qualifications

• 4+ years of Project Management experience in a professional setting.
• Experience in an FDA-regulated environment.
• Knowledge of project management methodologies.

Responsibilities

• Lead project planning, scheduling, execution, and delivery.
• Manage timelines, budgets, risks, and project documentation.
• Coordinate cross-functional teams across multiple sites.

Skills

Project Management

Communication skills

Leadership skills

Organizational skills

Problem-solving skills

Tools

MS Project

Excel

PowerPoint

Word

Outlook

SharePoint

Job description

Senior Project Manager – R&D / Medical Device

We are seeking a Senior Project Manager to support the Consumables R&D organization across Infusion, Oncology, Vascular Access, and Pain Management business units. This role will manage complex cross‑functional projects in an FDA‑regulated environment and partner with teams including R&D, Quality, Regulatory, Operations, Supply Chain, Marketing, and Medical Affairs.

Responsibilities:

• Lead project planning, scheduling, execution, and delivery
• Manage timelines, budgets, risks, and project documentation
• Coordinate cross‑functional teams across multiple sites
• Provide project status updates to leadership and stakeholders
• Support design control activities and manufacturing processes
• Ensure projects are completed on time and within budget

Requirements:

• 4+ years of Project Management experience
• Experience in an FDA‑regulated environment
• Knowledge of project management methodologies
• Familiarity with design controls and manufacturing processes
• Strong communication, leadership, and organizational skills
• Proficiency with MS Project, Excel, PowerPoint, Word, Outlook, and SharePoint

Preferred:

• Medical Device, Healthcare, Pharma, or Life Sciences experience