Senior Program Manager

Judge Direct Placement; Milford (OH); On-site; USD 160,000 - 175,000; Full time

Benefits offered by this job

Relocation assistance

Job summary

The Judge Group is seeking a Senior Program Manager in the Milford, OH area with strong experience leading Product Development Programs in medical device, pharmaceutical, or combination product environment.

The role requires 8+ years in regulated manufacturing, cross-functional leadership, and strong design control knowledge. Onsite work only with relocation available for the right candidate. US citizen or GC required.

Qualifications

• Bachelor of Science in Engineering or Life Science, etc.
• 8+ years of experience in Medical Device or Pharmaceutical manufacturing with ISO, FDA, MDD, and/or other healthcare industry regulations
• 3+ years of experience in product development activities and processes leading cross-functional, matrixed teams

Responsibilities

• Manage full life-cycle management partner programs
• Support Design Control principles (Gate reviews, freezes, Design reviews, Change management, approvals)
• Set and track project KPI (Strategy, Regulatory pathway, Clinical build progress, status, Schedule, Allocate resources, risk)
• Maximize relationships with external partners (Pharmaceutical, Healthcare)

Education

Bachelor of Science in Engineering or Life Science, etc

Job description

The Judge Group is seeking a Senior Program Manager in the Milford, OH area with strong experience leading Product Development Programs in medical device, pharmaceutical, or combination product environment.

COMPENSATION

160k to 175k

WORKSITE

Onsite (NO REMOTE)

RELOCATION

Available for the right candidate

MUST HAVE

Bachelor of Science in Engineering or Life Science, etc

MUST HAVE

8+ years of experience in Medical Device or possibly Pharmaceutical manufacturing with ISO, FDA, MDD, and/or other healthcare industry regulations

MUST HAVE

3+ years of experience in product development activities and processes leading cross-functional, matrixed teams

LIKE TO HAVE

PMP, CAPM, CPMP

MUST BE

A US Citizen or a Green Card Holder

EXPERIENCE

• Manage full life-cycle management partner programs
• Support Design Control principles (Gate reviews, freezes, Design reviews, Change management, approvals)
• Set and track project KPI (Strategy, Regulatory pathway, Clinical build progress, tatus, Schedule, Allocate resources, risk)
• Maximize relationships with external partners (Pharmaceutical, Healthcare)

QUALIFICATIONS

• 8+ years of experience in Medical Device or possibly Pharmaceutical manufacturing with ISO, FDA, MDD, and/or other healthcare industry regulations
• 3+ years of experience in product development activities and processes leading cross-functional, matrixed teams