Senior Program Manager (Med Device) (1145294)

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

Benefits offered by this job

Relocation assistance

Job summary

The Judge Group seeks a Senior Program Manager in Milford, OH to lead product development programs within medical device or pharmaceutical environments. The role is onsite with relocation available for the right candidate.

Requirements include a BS in Engineering or Life Science, 8+ years in regulated manufacturing, and 3+ years guiding cross-functional product development efforts. PMP/CAPM/CPMP are nice-to-haves.

Qualifications

• Bachelor of Science in Engineering or Life Science required.
• 8+ years in medical device or pharmaceutical manufacturing with ISO, FDA, MDD, or other healthcare regulations.
• 3+ years leading cross-functional product development activities.

Responsibilities

• Manage full life-cycle management of partner programs.
• Support Design Control principles (Gate reviews, freezes, Design reviews, Change management, approvals).
• Set and track project KPIs (strategy, regulatory pathway, clinical build progress, status, schedule, allocate resources, risk).
• Maximize relationships with external partners in Pharma and Healthcare.

Skills

8+ years in medical device/pharma

3+ years product development lead

Cross-functional leadership

Education

Bachelor of Science in Engineering or Life Science

Job description

Location: Milford, OH

Salary: $160,000.00 USD Annually - $175,000.00 USD Annually

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
• 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

LIKE TO HAVE:

PMP, CAPM, CPMP

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

• BS in Engineering / Life Science, etc.
• 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

LIKE TO HAVE:

PMP, CAPM, CPMP

#jdp

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Contact: [e-mail]

This job and many more are available through The Judge Group. Find us on the web at www.judge.com