
11 - 50 employees
Founded 2013
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
Pharmavise Corporation is the first Continuous Compliance Organization (CCO) dedicated to maintaining the highest standards of quality and regulatory compliance in the life sciences industry. Our esteemed client base includes Fortune 500 companies in pharmaceuticals, medical devices, and biotechnology. We offer bespoke solutions tailored to meet the specific compliance needs of our clients, supporting them from development through commercialization and ensuring they exceed their compliance goals while enhancing patient health and safety.
🕒 October 23, 2025
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11 - 50 employees
Founded 2013
🧬 Biotechnology
💊 Pharmaceuticals
⚕️ Healthcare Insurance
Biotechnology • Pharmaceuticals • Healthcare Insurance
Pharmavise Corporation is the first Continuous Compliance Organization (CCO) dedicated to maintaining the highest standards of quality and regulatory compliance in the life sciences industry. Our esteemed client base includes Fortune 500 companies in pharmaceuticals, medical devices, and biotechnology. We offer bespoke solutions tailored to meet the specific compliance needs of our clients, supporting them from development through commercialization and ensuring they exceed their compliance goals while enhancing patient health and safety.
• Lead the planning and execution of medical device product development and commercialization projects from concept through launch. • Define project scope, objectives, deliverables, and success criteria in collaboration with cross-functional stakeholders. • Develop and maintain detailed project plans, timelines, resource allocations, and budgets. • Ensure alignment between project goals and organizational strategy through effective stakeholder management. • Serve as the primary liaison among R&D, Quality, Regulatory, Manufacturing, and Supply Chain teams to ensure seamless project execution. • Manage change control processes and ensure that design and process changes are properly evaluated, documented, and approved. • Identify potential project risks and mitigation strategies, maintaining proactive issue resolution throughout the project lifecycle.
• 5+ years of experience in a regulated medical device, biotechnology, or pharmaceutical environment • Bachelor’s degree in Engineering, Life Sciences, Project Management, Business, or a related field • Proven experience managing projects in a regulated medical device, biotechnology, or pharmaceutical environment • Strong understanding of product development processes, design control, and risk management (ISO 14971) • Proficiency with project management tools such as MS Project, Smartsheet, or equivalent. • Excellent communication, documentation, and stakeholder management skills. • Strong problem-solving, analytical, and organizational abilities.
• Health insurance • 401(k) matching • Flexible work hours • Paid time off • Remote work options
Apply Now🕒 October 15, 2025
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