
About this role
PerkinElmer is an experienced leader in scientific solutions with a global service network and over 80-year legacy of advancing science. The Validation Engineer I is a full-time salaried position with Project Farma, requiring residence in the New Jersey market and willingness to travel domestically. This fully billable role supports biomanufacturing projects across the engineering lifecycle.
The Engineer I collaborates with clients, vendors, contractors, and team members to deliver high-quality work. Responsibilities include executing site strategy for CQV services and building relationships with key project points of contact. Identifies client needs during execution and communicates them to the Manager.
Works in a collaborative environment fostering long-term client relationships and technical knowledge growth. Participates in business development by attending industry events and supporting proposals. Maintains site dashboards to communicate project health and opportunities.
Supports talent development by encouraging best practices and accountability within the team. Ensures high-quality GMP Engineering services meet client specifications, regulatory requirements, and standards. Leads project initiatives from planning to closeout while escalating issues for resolution.
Requirements
- Reside in the New Jersey market
- Willing to travel domestically to meet client project requests
- Knowledge of biomanufacturing engineering lifecycle
- Ability to deliver GMP-compliant validation services
- Familiarity with CQV processes in pharmaceutical projects
- Technical proficiency in regulatory-compliant engineering delivery
- Client-facing experience in project execution and relationship management
Responsibilities
- Execute the site strategy as defined by the Manager to support leadership in CQV services
- Identify client needs during project execution and communicate to the Manager
- Build and maintain relationships with key project points of contact for smooth delivery
- Participate in project extensions, proposal generation, and business development initiatives
- Attend market-based industry events to build a local network
- Ensure delivery of high-quality GMP Engineering services meeting regulatory requirements
- Support project execution from planning to closeout, ensuring timelines and budgets are met
- Lead, oversee, and execute client project initiatives, plans, or workstreams
Benefits
- Full-time salaried position
- Support of a global service network and distribution centers
- Collaboration with commercial, government, academic, and healthcare customers
- Access to broad portfolio of analytical solutions and OneSource services
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