5 - 10 years
7 - 12 Lacs
Posted:13 hours ago|
Platform:
Work from Office
Full Time
Job Description
Roles & Responsibilities
Collaborate with cross-functional teams to define, plan, and execute manufacturing programs for new product introductions, process improvements, and production ramp-ups.
Develop comprehensive program plans, including scope definition, resource allocation, risk management strategies, and detailed timelines.
Monitor program progress against established milestones, identifying potential roadblocks and implementing proactive solutions.
Manage program budgets, track expenses, and ensure adherence to financial targets, identifying opportunities for cost optimization.
Partner with R&D, Engineering, Quality, Supply Chain, and Operations teams to ensure seamless integration and execution of program deliverables.
Establish and maintain clear communication channels with all stakeholders, providing regular updates on program status, risks, and mitigation plans.
Ensure all manufacturing processes and products comply with relevant regulatory requirements (e.g., FDA, ISO 13485) and internal quality standards.
Champion continuous improvement initiatives within manufacturing programs, identifying opportunities for process optimization and efficiency gains.
Facilitate problem-solving efforts and root cause analysis for manufacturing-related issues, implementing sustainable solutions.
Support and develop team members, fostering a culture of collaboration, innovation, and shared success.
Basic Qualifications
Bachelors degree in Engineering (Mechanical, Electrical, Biomedical, Industrial) or a related technical field. Masters degree preferred.
Minimum of 5+ years of experience in manufacturing , including at least 3 years in program management (experience with global locations, transfer program execution, or NPI) within the medical device industry.
Demonstrated ability to manage complex manufacturing programs from initiation through successful completion.
Desired Qualifications
PMP or equivalent certification preferred
Experience in the healthcare or medical device industry
Strong understanding of medical device regulations (e.g., FDA 21 CFR Part 820, ISO 13485) and quality management systems.
Proficiency in program management methodologies and tools (e.g., Gantt charts, critical path analysis, risk registers). PMP or equivalent certification highly desirable.
Excellent leadership, communication, and interpersonal skills, with the ability to influence and motivate cross-functional teams.
Proven ability to manage multiple priorities in a fast-paced, dynamic environment.
Strong analytical and problem-solving skills, with a data-driven approach to decision-making.
Experience with lean manufacturing principles and Six Sigma methodologies is a plus.
Proficiency in enterprise resource planning (ERP) systems and manufacturing execution systems (MES).
WIPRO GE HEALTHCARE PRIVATE LIMITED
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