Description

Lake County - Hybrid - onsite during our collaboration days (Tu-Th).

PhD will be overqualified

Bachelors or masters will work

Open for non local candiates who are ready to relocat at their own expense

Candidate will have engineering or biological science background

Medical device exp preferred but will consider pharma as well (medical device will be given first preference)

Medical Device product development role

• Organizational skills and communication skills
• Managing program on R&D or operations side
• Leading a core team of technical engineers, lab verification people, lab folks, quality assurance etc
• Will be keeping track of program
• Will be a part of design control process
• Will work on design control, verification testing
• 8 yrs exp needed
• Design control exp is a must have
• Device development space in R&D needed
• Medical Device industry exp
• Combination product exp
• Lead though design development phase
• Medical device pharma exp needed
• Have a lot of projects that this individual will support (Complex projects
• Develop timelines
• Will work on financial budgeting
• Provide update to various level of organization
• Any medical device projects or Device development programs will be helpful
• Sustainability engineer and change control and R&D or operations exp is helpful
• Medical device industry exp candidates without combination product exp will also work

2 year assignment 

• The Project Manager, Combination Products Development is accountable for leading the cross functional team (Engineering, Quality, Supply Chain, Marketing, Operations, Human Factors, and External Partners) in the execution of a portfolio of projects focused on the delivery system constituent parts of a combination product (Devices, Accessories, Instructions for Use, etc.).
• The Project Manager ensures that the strategy and plans defined for assigned programs are aligned with the needs of the patient and customer and the business objectives of the CMC and Product Strategy teams.
• In addition, product development timing and scope need to support plans for CMC gate reviews and each clinical phase.

Summary of Responsibilities and Accountabilities:

• The Project Manager will be accountable to the Program Manager Director for delivering on the strategy, plans and budget defined for the project portfolio.

Responsibilities include:

• Leadership of a portfolio of drug delivery system product development projects
• Tactical and strategic management of external device partners including acting as a key interface, managing the project governance process and forward-looking evaluation of potential partners
• Device financial management including budgeting, forecasting and long-range planning of delivery development expenses
• Representing the R&D organization to cross functional leadership through effective and timely communication
• Ensuring effective use of meetings by clearly defining objectives, agendas, inviting the team members specifically needed and publishing minutes and actions

Qualifications

Basic:

• Required: Bachelor’s Degree in Engineering or related technical field
• Certification: Project Management Professional (PMP) Certification preferred, but not required
• 8+ years of experience in the combination product or medical device industry with proven experience in developing medical devices or combination products; broad experience in design controls, human factors studies, design verification/validation and usability studies.
• Leadership of technical professionals; proven effective leader to cross-functional teams
• Skilled in the initiation, selection, coordination and management of projects and have the ability to solve unique problems.
• Requires an in-depth understanding of the pharmaceutical and device product development cycle.
• Design history file, project management and product development experience is essential.
• Conflict resolution skills including persuasive management techniques required. Effective communication and people management capability.