Sr. Project Manager

NexternCartago, Cartago ProvinceOn-siteFull-timeSenior, 5–8 yearsListed 1 week ago

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About this role

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