Pharmavise Corporation

Senior Project Manager — Medical Device (Hybrid — Arden Hills, MN) Possible Temp-to-Hire

Pharmavise Corporation  •  Saint Paul, MN (Hybrid)  •  4 months ago
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Job Description


Our F500 Medical Device client has an
exciting opportunity for a Senior Project Manager.


Job Summary:


This role
manages the development and implementation of cross functional projects that
support medical device Quality organization, with a focus on cardiology
products once they are out on the market. Operating across global sites (US MN,
Ireland, Costa Rica), this position ensures high quality execution of project
initiatives tied to medical device post market surveillance, medical device
risk management, and medical device manufacturing quality operations.


As the first
dedicated project manager that serves a team with ~50 key leaders, the
individual will independently establish project management structure and play a
key role in incorporating project management methodologies into the
organization. The role requires strong collaboration, proactive communication,
and the ability to understand complex interdependencies across multiple
projects to drive prioritization, execution, and patient centric outcomes. This
role does not require technical knowledge of the functional work performed by
the Quality organization but will need to obtain working knowledge of the
processes in place to best serve the cross-functional teams.


Key
Responsibilities:


Project
Planning & Execution


• Estimate
project level of effort and resource needs using standard project management
techniques and tools.


• Prepare and
maintain project plans, schedules, and budgets using Microsoft Project and
related project management tools.


• Direct
project execution by assigning tasks, tracking progress, identifying risks, and
implementing contingency plans.


• Resolve
project related issues in collaboration with team members and stakeholders.


Cross
Functional Leadership & Stakeholder Engagement


• Work across
key Quality functions to identify organizational priorities, project needs, and
stakeholder expectations.


• Conduct
regular check ins with project leaders to understand their goals, ensure
alignment to business needs, and monitor progress.


• Hold team
members accountable to timelines and escalate risks when necessary.


• Proactively
engage stakeholders to understand requirements and maintain strong
relationships.


• Monitor
resource allocation across the organization.


Metrics,
Reporting & Communication


• Define,
obtain, and monitor key organizational performance metrics.


• Partner
with data analysts to generate and visualize project performance dashboards.


• Deliver
clear, concise communication to leadership through status updates, monthly and
quarterly reviews, and management level storytelling.


Quality &
Compliance


• Maintain
compliance with the Quality Policy and all documented procedures, demonstrating
commitment to patient safety and product quality.


• For
supervisory scenarios: ensure adequate resources and foster a work environment
supporting Quality System compliance.


Project
Management Expertise & Continuous Improvement


• Apply
standard methodologies to assure project quality and drive consistent
execution.


• Mentor
project leaders and share project management knowledge across internal teams.


• Understand
project interdependencies and provide recommendations on prioritization to
support business needs.


Qualifications:


5+ Years with
BA; 3+ Years with MBA


• Estimates
project levels of effort and resource requirements by using standard estimating
techniques and tools, and by working with appropriate staff to understand scope
of effort.


• Prepares
project plans, schedules and budgets by using project management tools such as
Microsoft Project and by working with appropriate staff to understand tasks
necessary to complete project.


• Directs
project execution by assigning tasks, tracking project schedules, identifying
risks, and developing and executing contingency plans.


• Assures
project quality by using standard development methodologies to develop and
execute project quality plans.



Communicates project status by preparing standard status reports, and by
participating in departmental and customer project status update meetings.


• Resolves
project issues by working with team members, project customers, and others as
appropriate.


• Consults
with internal project groups by sharing project management knowledge and
assisting or mentoring more junior project leaders in project management
processes and techniques.



Participates in external project management organizations, conferences and
seminars to keep current with industry best practices in project management by
joining professional associations and implementing a professional development
plan with focus on project management.


Excellent
communication, leadership, problem-solving, and interpersonal skills


Preferred:


PM
Certificate


Medical
device experience


Other
Details:


Schedule: 08:00:AM
- 04:30:PM


Work Setup: Hybrid
in Arden Hills, MN


Contract Length: 9
Months (2/16/2026 - 11/15/2026)
Pharmavise Corporation

About Pharmavise Corporation

♦𝐄𝐱𝐜𝐞𝐥𝐥𝐞𝐧𝐜𝐞 𝐭𝐡𝐫𝐨𝐮𝐠𝐡 𝐐𝐮𝐚𝐥𝐢𝐭𝐲♦: 𝐏𝐡𝐚𝐫𝐦𝐚𝐯𝐢𝐬𝐞, 𝐲𝐨𝐮𝐫 𝐬𝐭𝐫𝐚𝐭𝐞𝐠𝐢𝐜 𝐋𝐢𝐟𝐞 𝐒𝐜𝐢𝐞𝐧𝐜𝐞𝐬, 𝐇𝐞𝐚𝐥𝐭𝐡𝐜𝐚𝐫𝐞 𝐚𝐧𝐝 𝐆𝐨𝐯𝐞𝐫𝐧𝐦𝐞𝐧𝐭 𝐬𝐨𝐥𝐮𝐭𝐢𝐨𝐧𝐬 𝐩𝐚𝐫𝐭𝐧𝐞𝐫.

𝗔𝗯𝗼𝘂𝘁 𝘂𝘀 𝗜𝗻𝗳𝗼𝗿𝗺𝗮𝘁𝗶𝗼𝗻:

We provide high-quality, cost-effective people and process solutions for your Quality, Regulatory, Engineering, Clinical, and Healthcare needs. Our company mantra 𝐄𝐗𝐂𝐄𝐋𝐋𝐄𝐍𝐂𝐄 𝐭𝐡𝐫𝐨𝐮𝐠𝐡 𝐐𝐔𝐀𝐋𝐈𝐓𝐘. The safety and quality of the drugs and devices produced for patients are directly related to 2 things, 𝐑𝐎𝐁𝐔𝐒𝐓 𝐏𝐑𝐎𝐂𝐄𝐒𝐒 𝐚𝐧𝐝 𝐐𝐔𝐀𝐋𝐈𝐅𝐈𝐄𝐃 𝐏𝐄𝐎𝐏𝐋𝐄. 𝐖𝐞 𝐝𝐞𝐥𝐢𝐯𝐞𝐫 𝐛𝐨𝐭𝐡.

𝐃𝐢𝐟𝐟𝐞𝐫𝐞𝐧𝐭𝐢𝐚𝐭𝐨𝐫𝐬:

☑𝐇𝐢𝐠𝐡𝐥𝐲 𝐒𝐤𝐢𝐥𝐥𝐞𝐝 𝐓𝐞𝐚𝐦: Our team of experienced consultants with distinct backgrounds in life sciences, including scientists, researchers, and regulatory experts. The quality and expertise of our team significantly impact our client’s success.

☑𝐒𝐩𝐞𝐜𝐢𝐚𝐥𝐢𝐳𝐞𝐝 𝐄𝐱𝐩𝐞𝐫𝐭𝐢𝐬𝐞: We focus on specific niches within the life sciences, healthcare, and government sectors, such as pharmaceuticals, biotechnology, medical devices, regulatory affairs, medical research, and product development. This specialized expertise allows us to offer targeted and in-depth insights to our clients.

☑𝐂𝐮𝐬𝐭𝐨𝐦𝐢𝐳𝐞𝐝 𝐒𝐨𝐥𝐮𝐭𝐢𝐨𝐧𝐬: We offer tailored solutions that align with the specific requirements of each client, rather than one-size-fits-all approaches, demonstrating a commitment to meeting client needs. We do not require a long learning curve, which leads to a faster payback and a greater return on your investment.

𝗣𝗲𝗿𝗳𝗼𝗿𝗺𝗮𝗻𝗰𝗲 𝗛𝗶𝘀𝘁𝗼𝗿𝘆

Over 20 Technical Transfers and 30 product launches.

11 FDA remediations. Warning Letters and or Consent Decrees.

Cost savings and increased efficiency of over 10MM for clients

Industry
Consulting & Advisory
Company Size
11-50 employees
Headquarters
Fort Lauderdale, Florida
Year Founded
2013
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