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Sr. Project Manager

  • Nextern
  • Cartago, Costa Rica
  • CRC 360,000 – CRC 540,000

This position will be responsible for coordinating new process-product development according to customer specifications, developing hands-on product solutions and supporting the business development cycle. It requires utilizing a collaborative approach to service new partners commercially and supports the new product introduction process for existing partners. It will also require working with a team approach by helping to improve manufacturing methods, systems and processes to produce a high-quality product at optimal cost. The Sr. Project Manager aids in managing a complete device project from the early concept, through Nextern’s detailed phase gate development, and through product manufacturing/commercialization.

DUTIES AND RESPONSIBILITIES:

  • Coordinates new product development with customers and internal project teams

  • Works with engineering team leads and management to create and tracks schedules, budgets, performance targets, resource plans, prioritization and delegation of tasks, and general planning activities for engineering deliverables

  • Provides visibility to project schedule and budget issues and manages escalation and coordinates critical issue resolution with project engineering Team Lead, Business Development Manager and Engineering Management

  • Provides the project management interface to project leads as well as critical internal and external (client) stakeholders for efficient coordination, execution of critical activities and project management functions

  • Ensures good cross-functional communication (through effective meetings, email, and other means) to ensure coordination between Engineering functional areas and other departments.

  • Review design and determine required bill of materials

  • Work with supply chain to obtain bill of materials pricing (from internal and external vendors)

  • Draft quotations and project scopes for review by management and delivery to customer.

  • Help to conduct component and device testing protocols.

  • Accurately generates standard written reports.

  • Help to develop plans to evaluate process repeatability and stability through equipment qualification and process validation.

  • Works with various departments and multiple manufacturing sites to facilitate pilot production of new products.

  • Ensures successful completion of project stages gates and related activities required for the projects to comply with the company compliant design and development process

  • Ensures proper documentation is completed for each development activity, and that adequate documentation exists for the Design History File, product manufacturing and ongoing production documentation.

  • Performs other related duties as assigned by management.

Requirements

  • Bachelor's Degree in BA, Engineering and five years of related experience in the medical industry.

  • 5+ years of experience as a Project Manager or similar roles

  • Previous experience (minimum of 4 years) in the technical field as a Process and/or Product Development R&D Engineer in the medical industry is a plus.

  • PMP Certification and/or a master’s degree in project management is a plus.

  • Fluent English 85-90% B2+ or C1

  • Able to provide guidance and mentoring to less-experienced team members.

  • Experience with FDA 510(k) process or other regulatory submissions preferred.

  • Adaptable to changing requirements and expectations but capable of identifying, communicating, and managing out of scope request and scope creep.

  • Critical leadership competencies, demonstrated ability to work on collaborative environments and excellence in managing teams and processes.

Benefits

Highly competitive package

Skills

  • Project Management
  • New Product Development
  • Phase/Gate Process
  • Budget Management
  • Cross-functional Team Leadership
  • Stakeholder Management
  • Manufacturing Processes

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