Program Manager
Found in: Whatjobs IN C2 - 3 weeks ago
We are seeking a highly skilled and experienced Program Manager with a strong background in the Health and Medical Device Manufacturing industry. The ideal candidate will have proven expertise in Shop floor management ,managing complex programs, leading cross-functional teams, and driving projects from conception to completion within the medical device manufacturing sector.
Key Responsibilities:
Program Leadership and Strategy:
- Lead the planning, execution, and delivery of multiple programs related to the development, manufacturing, and launch of medical devices.
- Develop comprehensive program strategies, objectives, and timelines in alignment with business goals and customer requirements.
- Provide strategic guidance and direction to cross-functional teams, ensuring clarity of objectives, roles, and responsibilities.
Cross-functional Team Management:
- Build and lead cross-functional teams comprising engineering, manufacturing, quality assurance, regulatory affairs, and other stakeholders.
- Foster a collaborative and high-performance team culture, promoting open communication, knowledge sharing, and problem-solving.
- Manage team dynamics, conflicts, and dependencies to ensure smooth project execution and achievement of program milestones.
Project Planning and Execution:
- Develop detailed project plans, schedules, and budgets, identifying critical path activities, resource requirements, and risk mitigation strategies.
- Monitor and track program progress, milestones, and key performance indicators (KPIs), proactively addressing deviations and ensuring timely delivery.
- Conduct regular project reviews, status meetings, and reporting to stakeholders, providing transparent and accurate updates on program status, risks, and opportunities.
Quality Assurance and Regulatory Compliance:
- Ensure compliance with relevant regulatory standards, industry guidelines, and quality management systems (e.g., ISO 13485, FDA regulations) throughout the product lifecycle.
- Collaborate with quality assurance and regulatory affairs teams to facilitate product registrations, submissions, audits, and certifications as required.
- Implement and maintain robust quality control processes, inspection procedures, and documentation practices to uphold product quality and safety standards.
Supplier and Contract Management:
- Manage relationships with suppliers, contractors, and external partners involved in the manufacturing and supply chain of medical devices.
- Should have experience in Procurement or Sourcing of Medical Devices components and parts.
Qualifications:
- Bachelor’s degree in Mechanical engineering , Bio Medical ,Life Sciences or related field; advanced degree preferred.
- Minimum of 12-15 years of experience in program management or leadership roles within the Health and Medical Device Manufacturing industry.
- Proven track record of successfully managing complex programs from initiation to completion, preferably in regulated environments (Manufacturing & Testing of medical devices Eg: CT, MRI , C Arm , Xray , Ultrasound etc.. ).
- Strong understanding of medical device development processes, manufacturing technologies, and regulatory requirements (e.g., FDA, CE Mark, ISO standards).
- Excellent leadership, communication, and interpersonal skills, with the ability to influence and collaborate effectively across diverse teams and stakeholders.
- PMP, Six Sigma, or other relevant certifications are a plus.
- Proficiency in project management tools, ERP systems, and Microsoft Office Suite.
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