Planet Pharma
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https://www.propharmagroup.com
https://www.propharmagroup.com
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Quality Project Manager, Cell and Genetic Therapies
225A Carolina Avenue Providence, RI 02905 US
Posted: 04/12/2024
2024-04-12
2024-08-14
Employment Type:
Contract
Job Category: Quality and Compliance
Job Number: 603786
Is job remote?: Yes
Country: United States
Job Description
Target PR Range: --
*Depending on experience
Job Title: Quality Project Manager, Cell and Genetic Therapies (Contract)
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Hours: 40 Hours per week, minimum 3 days on site.
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Location: Providence RI
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Summary:
This Quality Project Manager will be responsible for supporting cross-functional project teams executing Quality strategies within multiple programs. This individual will work with the Quality leads and interface directly with internal cross-functional teams. This individual will track, report, and project scope/timeline/milestone status associated with qualities projects, Team meetings and external meetings.
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This position is to drive plant implementation for the ISO 13485 and EU MDR regulatory requirements (European Medical Device Regulation. Must be able to effectively plan/track, collaborate, and manage the actions of different functions to deliver compliance to these regulations by the required deadlines.
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Responsibilities:
· Identify gaps against ISO 13485 and EU MDR requirements and lead on working on remediations the gaps.
· Work closely with area leads to develop and maintain integrated dashboards/ project plans.
· Identify/communicate interdependencies as well as critical path activities for the project(s).
· Track and monitor key milestones and decision points and work with team members to meet commitments and drive delivery of objectives.
· Be the central source of information for the project(s)
· Effectively communicate with team members, and key stakeholders on the status, objectives, risks, and mitigation plans associated with projects.
· Organize and maintain team communications including meeting agendas, minutes, decision logs, tasks lists, risk analyses/mitigation strategies, and other relevant materials using preferred technologies to support the project(s) teams.
· Update and maintain project status tools, such as a project action log, risk register, and dashboards.
· Assist in the creation and deployment of templates to manage team activities.
· Consistently perform duties within established SOPs, and in accordance with GxP requirements, where applicable.
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Qualifications:
· Bachelor’s degree in engineering, life sciences or related field. Advanced degree (MS, or MBA) and/or PMP Certification preferred.?
· A minimum of 6 years of experience in the biopharmaceutical or medical device industry.
· Previous experience of a minimum of 5 years in Quality/Manufacturing/Product Development or EU Medical Device Regulation (MDR) or CE Marking is required.?
· A minimum of 3 years of experience in project management of pharmaceutical or medical devices is required
· Experience interacting with Senior Management
· Working knowledge of cGMPs, and device development lifecycle.
· Ability to work effectively in a cross-functional, matrixed environment, prioritizing and managing multiple tasks simultaneously, integrating cross-functional issues and balancing competing priorities effectively.
· Experience independently developing complex project timelines, define project scope, convey timeline visuals (Gantt Charts)
· Ability to connect enterprise level strategy to project level objectives and clearly communicate and lead project deliverable to meet enterprise objectives and remove roadblocks.
· Expertise in Microsoft suite (Project, PowerPoint, SharePoint, Word, Excel, Outlook, Teams, OneNote, Visio, PowerBI). Experience with other PM tools a plus (e.g., Think-Cell, OnePager, Office Timeline, etc.).
· Candidates should possess individual and project organization skills, strong written and verbal communication skills, strong sense of urgency and accountability, ability to respond quickly to requests and efficiently follow up and drive project action completion, should thrive in a faced paced organization and comfortable managing high visibility projects.
*Depending on experience
Job Title: Quality Project Manager, Cell and Genetic Therapies (Contract)
Â
Hours: 40 Hours per week, minimum 3 days on site.
Â
Location: Providence RI
Â
Summary:
This Quality Project Manager will be responsible for supporting cross-functional project teams executing Quality strategies within multiple programs. This individual will work with the Quality leads and interface directly with internal cross-functional teams. This individual will track, report, and project scope/timeline/milestone status associated with qualities projects, Team meetings and external meetings.
Â
This position is to drive plant implementation for the ISO 13485 and EU MDR regulatory requirements (European Medical Device Regulation. Must be able to effectively plan/track, collaborate, and manage the actions of different functions to deliver compliance to these regulations by the required deadlines.
Â
Responsibilities:
· Identify gaps against ISO 13485 and EU MDR requirements and lead on working on remediations the gaps.
· Work closely with area leads to develop and maintain integrated dashboards/ project plans.
· Identify/communicate interdependencies as well as critical path activities for the project(s).
· Track and monitor key milestones and decision points and work with team members to meet commitments and drive delivery of objectives.
· Be the central source of information for the project(s)
· Effectively communicate with team members, and key stakeholders on the status, objectives, risks, and mitigation plans associated with projects.
· Organize and maintain team communications including meeting agendas, minutes, decision logs, tasks lists, risk analyses/mitigation strategies, and other relevant materials using preferred technologies to support the project(s) teams.
· Update and maintain project status tools, such as a project action log, risk register, and dashboards.
· Assist in the creation and deployment of templates to manage team activities.
· Consistently perform duties within established SOPs, and in accordance with GxP requirements, where applicable.
Â
Qualifications:
· Bachelor’s degree in engineering, life sciences or related field. Advanced degree (MS, or MBA) and/or PMP Certification preferred.?
· A minimum of 6 years of experience in the biopharmaceutical or medical device industry.
· Previous experience of a minimum of 5 years in Quality/Manufacturing/Product Development or EU Medical Device Regulation (MDR) or CE Marking is required.?
· A minimum of 3 years of experience in project management of pharmaceutical or medical devices is required
· Experience interacting with Senior Management
· Working knowledge of cGMPs, and device development lifecycle.
· Ability to work effectively in a cross-functional, matrixed environment, prioritizing and managing multiple tasks simultaneously, integrating cross-functional issues and balancing competing priorities effectively.
· Experience independently developing complex project timelines, define project scope, convey timeline visuals (Gantt Charts)
· Ability to connect enterprise level strategy to project level objectives and clearly communicate and lead project deliverable to meet enterprise objectives and remove roadblocks.
· Expertise in Microsoft suite (Project, PowerPoint, SharePoint, Word, Excel, Outlook, Teams, OneNote, Visio, PowerBI). Experience with other PM tools a plus (e.g., Think-Cell, OnePager, Office Timeline, etc.).
· Candidates should possess individual and project organization skills, strong written and verbal communication skills, strong sense of urgency and accountability, ability to respond quickly to requests and efficiently follow up and drive project action completion, should thrive in a faced paced organization and comfortable managing high visibility projects.
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