Sr Project Manager
- Pay
- $113,600 – $170,300 per year
- Location
- Teterboro, NJ · On-site
- Job type
- Full-time
- Level
- Lead / Staff
- Experience
- 5+ years
- Education
- Bachelor's degree
- Listed
- 8 days ago
Skills & highlights for this role
- Project management
- Technical transfer
- Cross-functional team leadership
- Risk management
- Stakeholder communication
- Pharmaceutical manufacturing knowledge
Also useful
- PMP certification
- Sterile injectable drug product manufacturing
- MySupply
- SmartSheet
- Process validation
About the role
- Work Schedule
- First Shift (Days)
- Environmental Conditions
- Office
About the role
Discover Impactful Work
The Project Manager is responsible for leading the successful execution of sterile injectable drug product technical transfer projects from initiation through commercial manufacturing. This role is accountable for managing assigned client projects, ensuring technical, operational, timeline, budget, and quality objectives are achieved while delivering a strong customer experience.
As a client-facing project lead, the Project Manager serves as a primary point of contact for assigned projects, maintaining clear and timely communication with client stakeholders and internal cross-functional teams. This includes aligning stakeholders on project scope, milestones, deliverables, risks, action items, and key decisions, while proactively managing expectations and escalating issues as appropriate.
The Project Manager partners closely with cross-functional teams to drive project execution, support risk mitigation, facilitate project meetings and decision-making, track progress against approved plans, and ensure successful delivery throughout the project lifecycle. This position requires strong project management skills, technical understanding of pharmaceutical manufacturing, effective communication, and the ability to influence across multiple functional areas while representing the organization professionally with external clients.
We have 2 positions available.
Day in the Life
- Independently manage multiple assigned sterile injectable technical transfer projects for client accounts.
- Serve as the primary point of contact for assigned customers, building trusted partnerships and ensuring clear, proactive communication throughout the project lifecycle.
- Develop, maintain, and communicate integrated project plans, timelines, deliverables, risks, and milestones.
- Ensure project deliverables and financial milestones are executed in accordance with contractual commitments and required timelines.
- Lead cross-functional project teams, including Manufacturing, MSAT, Quality, Validation, Regulatory, Supply Chain, and Engineering, to ensure successful project execution.
- Drive technical transfer activities from project initiation through process validation, regulatory support, and commercial launch/readiness, as applicable.
- Lead risk identification, mitigation planning, issue escalation, and resolution by coordinating appropriate internal resources.
- Act as the internal customer advocate while balancing business objectives and customer expectations.
- Facilitate project meetings, customer updates, technical discussions, site visits, and project-level governance reviews as needed.
- Monitor project financial performance, including milestone achievement, accrual inputs, bill-backs, service charges, and forecast updates in partnership with Finance and Commercial teams.
- Ensure project activities are managed in alignment with contractual obligations between Thermo Fisher Scientific and clients.
- Utilize MySupply, SmartSheet, and other project management tools to monitor project health, identify variances, implement corrective actions, and communicate project status to stakeholders.
- Prepare and deliver accurate project reports, dashboards, status updates, and stakeholder communications.
- Share best practices and support onboarding or coaching of less experienced project managers as opportunities arise.
- Support additional project-related initiatives and continuous improvement activities as assigned.
Education
- Bachelor's degree in Science, Engineering, Pharmacy, Business, or a related discipline required.
- PMP certification or equivalent project management certification preferred.
Experience
- Minimum of 5 years' experience within the pharmaceutical industry.
- Experience managing sterile injectable drug product manufacturing and technical transfers strongly preferred.
Knowledge, Skills & Abilities
- Strong understanding of pharmaceutical manufacturing, sterile injectable processes, technology transfer, and commercial launch readiness.
- Excellent project planning, organization, and prioritization skills with the ability to manage multiple competing priorities.
- Exceptional client-facing communication, stakeholder management, and relationship-building skills.
- Proven ability to identify risks, develop mitigation strategies, and lead issue resolution.
- Demonstrated leadership and influencing skills without direct authority.
- Proficiency with Microsoft Office applications, Smartsheet, MySupply, and other project management tools.
- Demonstrated commitment to Thermo Fisher Scientific's values of Integrity, Intensity, Innovation, and Involvement.
Excellent Benefits
- Benefits & Total Rewards | Thermo Fisher Scientific
- Medical, Dental, & Vision benefits-effective Day 1
- Paid Time Off & Designated Paid Holidays
- Retirement Savings Plan
- Tuition Reimbursement
Other
- Relocation assistance is NOT provided
- Must be legally authorized to work in the United States now or in the future, without sponsorship
- Must be able to pass a comprehensive background check, which includes a drug screening
Compensation and Benefits
The salary range estimated for this position based in New Jersey is $113,600.00–$170,300.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
- 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
From Thermofisher's careers page, first listed on Rolev.ai on November 6, 2026. Rolev.ai is not the employer.
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Common questions
What is the salary for the Sr Project Manager role at Thermofisher?
The Sr Project Manager posting at Thermofisher states compensation of $113,600 – $170,300 per year. It is listed as a full-time position. Final pay may depend on location, experience, and interview evaluation on Thermofisher's official career site.
Where is the Sr Project Manager job at Thermofisher located?
This Sr Project Manager position at Thermofisher is located in Teterboro, NJ (On-site). Always check Thermofisher's application page for specific state eligibility or relocation policies.
What qualifications are required for Sr Project Manager at Thermofisher?
For the Sr Project Manager role, Thermofisher highlights 5+ years of relevant experience; a bachelor's degree; experience with Project management, Technical transfer, Cross-functional team leadership, Risk management, Stakeholder communication, Pharmaceutical manufacturing knowledge. Rolev.ai can score your existing resume against these requirements and show any skill gaps before you apply.
How do I apply for the Sr Project Manager position at Thermofisher?
This listing links directly to Thermofisher's Workday application page. You can apply directly on Thermofisher's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Workday application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.