Sr Program Manager

MissionStaff; Malvern (Chester County); On-site; USD 130,000 - 170,000; Full time

Job summary

MissionStaff is seeking a Sr Program Manager to lead engineering and cross-functional teams through the entire product development lifecycle for regulated medical device programs. The role requires coordinating hardware and software efforts, managing risk, and ensuring milestones meet quality and regulatory standards.

You should have deep knowledge of product development processes and regulations (FDA QSR, GMP, ISO 60601/13485/14971), strong communication, and a history of delivering complex

Qualifications

• Knowledge of product development processes and dependencies.
• Familiarity with FDA QSR, GMP, and ISO regulations (60601, 13485, 14971).
• Strong communication and problem-solving skills; Six Sigma certification preferred.

Responsibilities

• Lead engineering and cross-functional teams through the full product lifecycle.
• Drive on-time, on-budget delivery with high quality and regulatory compliance.

Skills

Product development

Regulatory knowledge

Cross-functional leadership

Embedded & cloud software

Communication & problem solving

Education

Bachelor of Science in Engineering

Job description

We connect top talent in Business Services, Tech, Marketing & Creative with companies of all sizes—offering flexible, high-touch staffing solutions. We are currently filling the following direct-hire job for our client.

Job Title: Sr Program Manager

Overview:

This highly visible role offers an exciting opportunity to lead engineering and cross-functional teams through the entire product development lifecycle, including new product introduction, installed base programs, and product lifecycle management. Perfect for candidates with R&D and software development experience, the Sr Program Manager will be a vital right-hand to the leadership team, driving innovative, market-leading solutions in a regulated industry. The role involves strategic collaboration, risk mitigation, and ensuring timely, on-budget delivery with high quality and compliance.

Required Skills:

• Extensive knowledge of product development processes and dependencies
• Familiarity with FDA QSR, GMP, and ISO regulations (60601, 13485, 14971)
• Strong communication and problem-solving skills, preferably with Six Sigma certification or equivalent
• Demonstrated ability to build and lead cross-functional teams and resolve conflicts
• Experience with hardware and software applications, including embedded and cloud-based platforms

Nice to Have Skills:

• R&D and software development background, particularly in embedded or cloud software platforms
• PMP certification or equivalent project management credentials

Preferred Education and Experience:

• Bachelor of Science in Engineering or a related technical field
• 3+ years as a Program Manager in the medical device industry, managing full program lifecycles from concept to market launch
• 5+ years in regulated industries such as pharmaceutical, life sciences, aerospace, or military

MissionStaff is an equal opportunity employer. Please note that we do not accept unsolicited resumes from third-party recruiters or agencies. Additionally, candidates must be U.S. citizens or Permanent Residents to be considered for this position.