Job Description

Our F500 Medical Device client has an exciting opportunity for a Project Manager.
Summary:
We are looking for a talented business leader to join our Urology Project Management Organization (PMO). We have an exciting opportunity for a Senior Project Manager that will lead the Software Integration as part of various Product Integration workstreams associated with our recent Axonics Acquisition. In this role, you will lead cross-functional teams to execute the integration projects required to integrate the Axonics Product Portfolio into Client’s Systems. We are seeking an experienced candidate who has demonstrated software project management and effective cross-functional leadership experience. Prior experience managing software projects within the Medical Device field and experience with quality system and risk management process are preferred.
Responsibilities and Job Requirements:
• Provide Project Management leadership of a cross-functional Teams as part of the Axonics Integration, leveraging agile methodologies and common divisional processes and tools.
• Influence stakeholders and team members to drive alignment, develop plans and deliver results. Build team ownership and commitment to project plans.
• Partner and collaborate with a variety of functions to achieve project objectives. This includes identifying resources required for project activities, timeline development, and project prioritization.
• Communicate progress and status to Integration Lead.
• Prioritize, delegate, and manage tasks among projects and team members, as appropriate, to drive execution of project deliverables and minimize risk.
• Support development, implementation, and revision of detailed project plans, including deliverable lists, risk management, communication plans, etc.
• Ensure Client policies and practices are followed.
Minimum Qualifications
• Bachelor’s Degree in Science, Engineering or Business and 5+ years of work experience in software, product development or related field AND
• 5+ years Project Management experience in the Medical Device industry
• Demonstrated project management experience leading cross functional teams and managing project scope, schedule, and budget
• Excellent organizational, interpersonal, and communication skills (verbal written, and presentation)
• Results-oriented, positive attitude focused on delivering timely, accurate and best in class execution
• Ability to draw conclusions and make business recommendations based on cross-functional team input
• Proficiency in MS Office applications including MS Project
• Proficiency in MS SharePoint
• Ability to travel intermittently (up to 20%) to support effective team performance and collaboration
Preferred Qualifications
• Experience with utilizing agile project management
• 5+ years Project Management experience managing software projects within the Medical Device field, knowledge and application of applicable software ISO and IEC standards in the project scope
• PMP Certification
Other Details:
• Location: Hybrid – Arden Hills, MN
• 20% travel
• Start Date: ASAP
• Contract Length: 12 months

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

Website

pharmavise.com

Social Media

Project Manager — Medical Device (Hybrid — Arden Hills, MN ) Contract

Job Description

About Pharmavise Corporation