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Process Engineer III – Lead Process Engineer
PerkinElmer. Participate in clients’ Global Engineering teams as an Owner’s Representative supporting pharmaceutical and biotechnology capital projects .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in process engineering and project oversight within pharmaceutical and biotechnology capital projects, ensuring compliance with GMP requirements and regulatory standards. Capable of leading cross-disciplinary teams and managing complex engineering deliverables while mentoring junior engineers.
Highest-signal resume keywords
Process Engineering ExpertiseGMP Manufacturing KnowledgePFDs and P&IDs DevelopmentOwner's Representative ExperienceProject Management in Capital Projects
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Process DesignTechnical LeadershipEngineering Deliverables ReviewEquipment SpecificationsProcess CalculationsMaterial BalancesUtility RequirementsRisk AssessmentsChange ManagementQualification and Validation Strategies
Soft Skills
Excellent Communication SkillsOrganizational SkillsInterpersonal SkillsAbility to Manage Multiple Priorities
Industry Keywords
Pharmaceutical EngineeringBiotechnologyCGMP Facility Start-UpArchitecture & Engineering CoordinationCapital Project ExecutionStakeholder EngagementConstruction and CommissioningGlobal EngineeringMatrixed OrganizationLife Sciences
About the role
Key responsibilities & impact- Participate in clients’ Global Engineering teams as an Owner’s Representative supporting pharmaceutical and biotechnology capital projects
- Provide technical leadership, project oversight, and process engineering expertise
- Oversee process design performed by Architecture & Engineering firms
- Ensure process concepts, user requirements, equipment selections, facility layouts, utilities, process flows, and engineering deliverables align with operational, technical, quality, regulatory, and business objectives
- Provide day-to-day technical oversight of A&E process engineering activities and deliverables
- Establish process engineering scope, design criteria, deliverables, and technical standards
- Review, challenge, and approve A&E process engineering deliverables
- Coordinate process engineering with architectural, mechanical, electrical, automation, structural, civil, environmental, and other disciplines
- Participate in design reviews, HAZOPs, risk assessments, constructability reviews, operability reviews, and value-engineering exercises
- Develop and/or review PFDs, P&IDs, equipment specifications, equipment layouts, process descriptions, and process design criteria
- Review equipment sizing, process calculations, material balances, utility requirements, and equipment data sheets
- Ensure process designs support GMP requirements and regulatory expectations
- Work with Quality, Manufacturing, Validation, Regulatory, EHS, and Operations functions
- Support qualification and validation strategies related to process and equipment design
- Represent Global Engineering in project meetings with stakeholders, A&E firms, vendors, contractors, and project partners
- Track technical issues, design decisions, action items, and engineering risks
- Support change management and assess technical impacts
- Participate in FATs, SATs, commissioning, startup, and qualification activities
- Support resolution of construction and commissioning issues
- Ensure final engineering documentation reflects the installed facility and equipment
- Mentor junior and peer engineers while remaining focused on technical delivery
Requirements
What you’ll need- Bachelor’s Degree in Life Science, Engineering, or related discipline, or a combination of equivalent work experience in capital project engineering, pharma cGMP facility start-up, CapEx/OpEx project management and/or comparable military experience
- Approximately 5–10 years of relevant pharmaceutical, biotechnology, or life-sciences engineering experience
- Demonstrated experience with pharmaceutical or biotechnology facility design, process engineering, or capital project execution
- Experience working with or managing Architecture & Engineering firms and/or engineering contractors
- Demonstrated ability to function effectively as an Owner’s Representative
- Strong understanding of GMP manufacturing environments and pharmaceutical engineering practices
- Ability to independently review and challenge process engineering deliverables
- Experience developing or reviewing PFDs, P&IDs, equipment specifications, layouts, process descriptions, and utility requirements
- Strong understanding of the relationship between process requirements and facility design
- Excellent written, verbal, organizational, and interpersonal communication skills
- Ability to manage multiple priorities in a global, matrixed organization
- Willingness to travel as required for client project assignments
- Applicants must be authorized to work in the United States on a full-time basis
- No current or future work visa sponsorship
- Cannot employ anyone with an invalid driver's license
Benefits
Comp & perks- Equal opportunity employer
- Diverse and culturally diverse workforce
- Significant travel to support project and business needs