Pharmavise Corporation

Project Specialist II — Medical Device (Hybrid — Maple Grove, MN) Possible Temp-to-Hire

Pharmavise Corporation  •  Maple Grove, MN (Remote)  •  1 month ago
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Job Description


Our Fortune 500 Medical Device client has an exciting opportunity for a Project Specialist II.


Job Summary:


The Project Specialist II will support the Interventional Spine Team within the Neuromodulation Division, which focuses on advancing solutions for chronic pain through the

Intracept

® Procedure — a minimally invasive, implant-free therapy designed to target and relieve chronic

vertebrogenic

low back pain by ablating the

basivertebral

nerve.

This dual-role position (Analyst / Project Specialist)

is responsible for

managing analytics and reporting activities, coordinating vendor and compliance processes, and developing high-quality presentation materials. The ideal candidate will be detail-oriented, organized, and skilled at managing multiple priorities in a fast-paced, data-driven environment.

Key Responsibilities

:


Purchasing

, Vendor & Compliance Coordination:

o Manage

purchasing

and vendor processes in alignment with company compliance requirements.

o Support vendor documentation and approval workflows to ensure operational efficiency.

• Market Research Management (Quantitative & Qualitative):

o Lead both quantitative (data-based) and qualitative (insight-driven) market research initiatives.

o Coordinate project timelines, vendor activities, and deliverables to ensure

timely

completion.

o Summarize findings and deliver insights in clear, presentation-ready formats.

• Analytics & Reporting:

o Generate and analyze data from Salesforce and Tableau to support business decisions.

o Maintain and refresh monthly and quarterly dashboards and reports

• Presentation Development & Slide Refinement:

o Translate analytical outputs into professional PowerPoint presentations.

o Apply

high standards

of design and accuracy to create polished, executive-level materials.

o Manage ongoing updates and refinements to ensure consistency across deliverables.

• Project & Operational Support:

o Provide analytical and project coordination support to the Interventional Spine commercial team.

o Manage ad hoc tasks and requests to support the team’s evolving business needs.

Quality Systems Responsibilities

:

Incorporate quality into all aspects of work by

maintaining

compliance with applicable quality system requirements and company standards.

Qualifications Required

:


Bachelor’s

degree with 2–3 years of relevant experience, or advanced degree with 0–1 year of experience.

• Experience in market research (both quantitative and qualitative) or consulting environments.


Proficiency

in analytic toolkits such as Excel and Pandas.

• Background in data analytics or computer science (Python experience

a plus

).

• Advanced PowerPoint skills with the ability to create refined, presentation-ready materials.

Preferred

:

• Project Management Certification (e.g., PMP, CAPM) preferred.

• IRB experience

• Experience with compliance and vendor coordination processes.


Other Details:


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


Work Setup:

Hybrid - 3 days onsite per week in Maple Grove, MN


Contract Length: 12 Months (

11/17/2025 - 11/16/2026

)

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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