Program Manager III – Transplant Diagnostics

Job not on LinkedIn

🔥 22 hours ago

⛰️ Colorado, Kansas, +3 more states – Remote

⛰️ Colorado – Remote 🌪️ Kansas – Remote 🎰 Nevada – Remote ⚔️ Virginia – Remote ⛰️ West Virginia – Remote

💵 $83.3k - $125k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

📋 Program Manager

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

Healthcare • Logistics • Manufacturing

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• Lead cross-functional project core teams, conduct regular project meetings, capture action items, supervise assigned deliverables, develop and maintain project schedules, and provide updates and reports to senior leadership • Work closely with R&D, Product Management, Manufacturing Sciences, and Manufacturing Operations, Quality, Regulatory, and other functional partners to develop high quality products that meet customer needs and regulatory guidelines • Collaborate with Finance and other business functions to develop project financial models and ensure positive return on investment • Maintain clear communication lines across all teams and stakeholders, providing regular updates on project status and achievements to executives, while resolving barriers to execution and facilitating decision making to ensure timely completion • Identify potential risks and issues, and develop effective mitigation strategies to maintain compliance, product quality, and project execution • Identify and champion opportunities for improvement in day-to-day processes, operating mechanisms, and procedures

🎯 Requirements

• University degree (Bachelor’s or Master’s degree), preferably in life sciences or engineering • Demonstrated experience leading teams without direct authority • 4 years experience in developing life-science products under design control, using a standard stage-gate process from conceptualization to launch; medical device and clinical experience highly preferred • Experience developing RUO and IVD assays, including clinical study performance, preferred • PMP certification is a plus

🏖️ Benefits

• A choice of national medical and dental plans, and a national vision plan, including health incentive programs • Employee assistance and family support programs, including commuter benefits and tuition reimbursement • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan • Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount