PSG Global Solutions Project Manager in North Haven, Connecticut
We're looking for a Project Manager , working in the Biotechnology/Medical Devices industry in North Haven, Connecticut .
Manage the implementation of cross-functional MDR requirements for portfolio products and priorities.
Schedule and act as a facilitator for core team and cross-functional meetings.
Provide ongoing maintenance to project plans, budgets, schedules.
Facilitate project risk management and ensure information is timely, factual, and accurate.
Partner with other business projects to ensure dependencies are accounted for.
Maintain program data systems containing key project indicators.
Mediate / facilitate cross-functional process understanding or improvements.
Seeks out and engages regularly with peers, creating an environment of exchange and learning.
Openly shares successes and failures to promote the groups collective learning.
Prepare regular status reports for the project team, management, or the corporate organization.
Perform escalation management as appropriate.
Work individually or in a team environment to complete objectives.
Complete all activities in compliance with the Quality System.
Performs duties in compliance with environmental, health and safety related site rules, policies or governmental regulations.
All other duties as assigned.
Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
Education and Experience:
8+ years with Bachelors degree Business Management, Engineering, or other related field of study, OR
6+ years with Masters degree in Regulatory Affairs, OR
A function familiar with technical files and medical device product development process
Solid PM implementation experience required
Minimum of 5 years of QARA and/or plant manufacturing or engineering experience, which includes a minimum of 5 years of demonstrated process improvement and project management success
Knowledge of standards, current European medical device directives (MDD/AIMDD), or CE mark process
Ability to work independently or collaboratively to determine and develop approaches to solutions
Experience driving initiative and change management across a BU
Excellent verbal, written communication and presentation skills
Experience delivering presentations at all levels in an organization
Experience influencing stakeholders at multiple levels in an organization
Experience with MS Project, Excel, PowerPoint, Word, SharePoint
Demonstrated ability to work successfully in complex business and project areas, leveraging interpersonal skills and technical skills to optimize results
Broad business knowledge and ability to link customer needs with business processes
Strong analytical problem-solving skills
Ability to support multiple projects and balance priorities
Ability to work independently and with all levels of managers, associates, and clients
Strong coaching, facilitation and organizational skills
Excellent oral/written communication and platform skills
The pay range we are offering is 60 to 70 per hour. This position may present an opportunity to go permanent.
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here .
Not exactly? Join Our Talent Community (https://jobs.psgglobalsolutions.com/register) , and we'll let you know of additional opportunities.
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