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Project manager iii (non-it)

Irvine
Permanent
Mindlance
Project manager
€83,333.6 a year
Posted: 2 February
Offer description

Overview

Location: Irvine, CA - Hybrid Required - (M/F Remote - T/W/TH Onsite) Non-negotiable

Contract: 2 years - based on performance and business needs

Location/Site – Irvine CA (US-CA-Irvine (RD II, 2525 B Dupont Drive) (S5156))

Work shift (days/times) – 9AM-5PM


Top skills and qualifications

* Leadership: Ability to motivate teams, delegate tasks effectively, and drive project success.
* Communication: Excellent written and verbal communication skills to manage stakeholders and team members.
* Risk Management: Expertise in identifying, assessing, and mitigating project risks.
* Scheduling & Organization: Proficiency in planning, prioritizing tasks, managing timelines, and using project management tools.
* Problem-Solving/Process Improvement: Strong analytical skills to resolve issues and adapt to changing project requirements.


Education

* Required: Bachelor’s degree in engineering (mechanical or biomedical engineering).
* Preferred: Master’s degree in engineering or management is preferred but not required.
* Certification: Project Management Professional (PMP) Certification preferred but not required.


Experience

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.


Position

Project Manager III (Non-IT)

________________________________________


Description

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.


Responsibilities

* 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:
o Required: Bachelor’s degree in engineering (mechanical or biomedical engineering). Master’s degree in engineering or management is preferred but not required.
o Certification: Project Management Professional (PMP) Certification preferred, but not required
o 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.
* Required Skills:
o Leadership: Ability to motivate teams, delegate tasks effectively, and drive project success.
o Communication: Excellent written and verbal communication skills to manage stakeholders and team members.
o Risk Management: Expertise in identifying, assessing, and mitigating project risks.
o Scheduling & Organization: Proficiency in planning, prioritizing tasks, managing timelines, and using project management tools.
o Problem-Solving/Process Improvement: Strong analytical skills to resolve issues and adapt to changing project requirements.
o Requires an in-depth understanding of the pharmaceutical and device product development cycle.
o Design history file, project management and product development experience is essential.


EEO

“Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.”

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