Project Manager- Medical Device

ALTEN; Gurugram District; Presencial; INR 1.800.000 - 3.200.000; Jornada completa

Descripción de la vacante

ALTEN in India is seeking a Project Manager- Medical Device with 9–12 years of experience to lead software projects from initiation to delivery. You will coordinate cross-functional teams, manage budgets, and drive on-time project completion in a regulated medical device environment.

Key responsibilities include risk identification with mitigation plans, clear stakeholder communication, and ensuring compliance with FDA and international medical device regulations. PMP certification is preferred.

Formación

• 9–12 years of experience in project management.
• Hands-on PM experience in software projects.
• PMP or equivalent certification preferred.
• Experience in Medical Device industry.
• Strong knowledge of FDA and international regulations.

Responsabilidades

• Lead and manage software projects, ensuring delivery on time and within budget.
• Identify risks and develop mitigation strategies with analytical skills.
• Communicate with cross-functional teams to meet requirements.
• Ensure compliance with FDA and international medical device regulations.

Conocimientos

Project leadership

Risk management

Stakeholder comms

Regulatory knowledge

Educación

PMP certification

Descripción del empleo

with Below details

CTC

ECTC

NP: Immediate joiner /15 days /Serving Candidate

Role: Project Manager- Medical Device

Description

• Lead and manage software projects, ensuring successful delivery on time and within budget


• Utilize excellent analytical and problem-solving skills to identify risks and develop mitigation strategies


• Communicate effectively with cross-functional teams to ensure project requirements are understood and met


• Apply knowledge of FDA & International medical device regulations to ensure compliance

Qualification Criteria

• Candidate should have 9 to 12 years of experience


• Hands-on experience in project management


• PMP or equivalent certification preferred


• Experience working in the Medical Device industry


• Strong understanding of FDA & International medical device regulations