Integra LifeSciences
Senior Project Manager - Plainsboro, NJ
Integra LifeSciences, Plainsboro, New Jersey, us, 08536
Changing lives. Building Careers.
Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what's possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.
The Sr. Project Manager is responsible for leading cross-functional teams in the planning, direction and execution of projects to drive efficiency, reduce waste and enhance overall performance to plan. This person will ensure clear communication with stakeholders in manufacturing, quality, engineering, product development, process technologies to ensure value stream performance to support Process Technologies projects in Tissue Technologies.
Project Leadership - lead cross-functional project teams to deliver value stream optimization projects on time, within scope, and on budget. Manage small, independent projects or specific workstreams within a large, complex program.
Continuous improvement mindset and process improvement applying lead six sigma methodologies to streamline processes, eliminate waste and increase productivity for the assigned value stream.
Risk Management - Identify potential risks and develop mitigation plans to address issues proactively and ensure project success.
Stakeholder collaboration and communication, working closely with maintenance, engineering, manufacturing, quality assurance, product development, process technology and supply chain teams to align project goals and ensure successful execution. Provide regular updates to senior management on project status, performance metrics, and improvement initiatives.
Participation in solving problems encountered within a project.
Work with a cross-functional team to assign and track key project activities clearly communicating industry standards and best practice requirements to cross-functional teams.
Constructing project timelines with refinement from value stream leadership, determining and monitoring resources to support a given project and building budgets with oversight from senior program managers
Performance metrics & change management - establish and monitor key performance indicators (KPIs) to track progress, measure success, and drive continuous improvement. Facilitate change management processes to ensure smooth transitions and stakeholder buy-in for process changes.
Quality and compliance - ensure all projects and processes adhere to regulatory requirements and industry standards for medical devices.
All production is conducted with Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating Procedures (SOP's), and Health and Safety requirements.
Qualifications:
Bachelor degree in Engineering, Science, Business, or equivalent with 5+ years of experience; Master degree with 3+ years of experience leading a team.
PMP certification preferred.
Experience leading cross-functional teams and project.
Experience in a manufacturing environment, preferably medical device or FDA regulated industry.
Must possess strong written, verbal and interpersonal skills.
Demonstrated organizational and communication skills. Must possess strong leadership skills with team-focused attitude and approach.
Strong computer skills, including Microsoft Office experience required.
Understanding and experience with Lean/six Sigma, certification preferred.
MUST BE LOCAL TO PLAINSBORO, NJ
Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.
This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices:
EEO Is the Law (https://www.eeoc.gov/laws/index.cfm) | EOE including Disability/Protected Veterans (https://www.eeoc.gov/eeoc/publications/ada_veterans_employers.cfm)
Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA (https://www.eeoc.gov/eeoc/publications/fs-ada.cfm) . If you have difficulty using our online system due to a disability and need an accommodation, please email us at careers@integralife.com or call us at 855-936-2666.
Integra - Employer Branding from Integra LifeSciences on Vimeo (https://player.vimeo.com/video/265760526)
Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what's possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.
The Sr. Project Manager is responsible for leading cross-functional teams in the planning, direction and execution of projects to drive efficiency, reduce waste and enhance overall performance to plan. This person will ensure clear communication with stakeholders in manufacturing, quality, engineering, product development, process technologies to ensure value stream performance to support Process Technologies projects in Tissue Technologies.
Project Leadership - lead cross-functional project teams to deliver value stream optimization projects on time, within scope, and on budget. Manage small, independent projects or specific workstreams within a large, complex program.
Continuous improvement mindset and process improvement applying lead six sigma methodologies to streamline processes, eliminate waste and increase productivity for the assigned value stream.
Risk Management - Identify potential risks and develop mitigation plans to address issues proactively and ensure project success.
Stakeholder collaboration and communication, working closely with maintenance, engineering, manufacturing, quality assurance, product development, process technology and supply chain teams to align project goals and ensure successful execution. Provide regular updates to senior management on project status, performance metrics, and improvement initiatives.
Participation in solving problems encountered within a project.
Work with a cross-functional team to assign and track key project activities clearly communicating industry standards and best practice requirements to cross-functional teams.
Constructing project timelines with refinement from value stream leadership, determining and monitoring resources to support a given project and building budgets with oversight from senior program managers
Performance metrics & change management - establish and monitor key performance indicators (KPIs) to track progress, measure success, and drive continuous improvement. Facilitate change management processes to ensure smooth transitions and stakeholder buy-in for process changes.
Quality and compliance - ensure all projects and processes adhere to regulatory requirements and industry standards for medical devices.
All production is conducted with Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating Procedures (SOP's), and Health and Safety requirements.
Qualifications:
Bachelor degree in Engineering, Science, Business, or equivalent with 5+ years of experience; Master degree with 3+ years of experience leading a team.
PMP certification preferred.
Experience leading cross-functional teams and project.
Experience in a manufacturing environment, preferably medical device or FDA regulated industry.
Must possess strong written, verbal and interpersonal skills.
Demonstrated organizational and communication skills. Must possess strong leadership skills with team-focused attitude and approach.
Strong computer skills, including Microsoft Office experience required.
Understanding and experience with Lean/six Sigma, certification preferred.
MUST BE LOCAL TO PLAINSBORO, NJ
Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.
This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices:
EEO Is the Law (https://www.eeoc.gov/laws/index.cfm) | EOE including Disability/Protected Veterans (https://www.eeoc.gov/eeoc/publications/ada_veterans_employers.cfm)
Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA (https://www.eeoc.gov/eeoc/publications/fs-ada.cfm) . If you have difficulty using our online system due to a disability and need an accommodation, please email us at careers@integralife.com or call us at 855-936-2666.
Integra - Employer Branding from Integra LifeSciences on Vimeo (https://player.vimeo.com/video/265760526)