Are you looking to build a career in validation, commissioning, and qualification (CQV) within the pharmaceutical / life sciences industry? We’re hiring a Validation Engineer / Validation Specialist who wants hands-on experience across IQ, OQ, PQ, exposure to real projects, and a clear path into leadership. This is an opportunity to grow quickly in a GMP-regulated environment, working alongside experienced engineers while taking ownership of meaningful validation work.

What You’ll Do

• Execute and support IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) protocols
• Work on validation of lab systems, equipment, and utilities
• Partner with engineering, validation teams, and lab stakeholders
• Assist with project scheduling, coordination, and resource planning
• Support commissioning & qualification (CQV) activities across projects
• Contribute to GMP / GxP documentation and compliance efforts
• Learn to lead validation workstreams and progress into a Validation Engineer / Project Lead role

What We’re Looking For

• 2+ years of experience in:
  • Validation Engineering
  • CQV (Commissioning, Qualification, Validation)
  • or GMP-regulated environments (Pharma / Biotech)
• Strong understanding of:
  • GMP / GxP / FDA regulations
  • Validation lifecycle (IQ/OQ/PQ)
• Ability to work cross-functionally with engineering, QA, and operations teams
• Strong communication and problem-solving skills
• Coachable, driven, and motivated to grow into leadership

Requirements

• Bachelor’s degree in Engineering, Life Sciences, or related field
• Willingness to travel regionally (project-based work)
• Experience with validation documentation, protocols, and execution

Nice to Have

• Experience with lab systems, utilities, or manufacturing equipment validation
• Exposure to commissioning activities (C&Q / CQV)
• Familiarity with AI tools for validation or documentation

Why This Role

• Hands-on experience across pharma validation projects
• Clear path into senior validation or project leadership roles
• Work alongside experienced engineers in regulated environments
• Real ownership early in your career 

Validation Engineer, Validation Specialist, CQV Engineer, Commissioning Engineer, Qualification Engineer, GMP Validation, GxP, IQ OQ PQ, Pharmaceutical Validation, Life Sciences Validation, Equipment Validation, Utilities Validation, Computer System Validation, CSV Engineer, FDA Compliance, GMP Engineer

• Location: St. Louis (Field-Based)
• Compensation: $60-$80k + bonus + benefits

Are you a seasoned Calibration Technician who thrives in complex environments and knows how to solve problems without waiting for direction?

We’re hiring a Senior Calibration Technician in the Greater St. Louis area to support advanced installations, troubleshooting, and client-facing technical work. This is a high-impact role for someone who can step into the field, assess issues quickly, and deliver solutions with confidence.

If you have strong experience with networking, sensors, or technical systems, and you’re comfortable owning projects independently, this is built for you.

What You’ll Do

• Lead installation, configuration, and maintenance of technical systems in the field
• Troubleshoot complex networking, sensor, and system-level issues in real-time
• Serve as the on-site technical expert for clients and internal stakeholders
• Handle escalations and resolve high-priority technical challenges
• Work independently to assess environments, identify risks, and implement solutions
• Document field activity, system performance, and resolutions clearly

What We’re Looking For

• 3+ years of experience as a Field Technician, Field Service Technician, or similar role
• Strong background in troubleshooting, installation, and system diagnostics
• Experience with networking (IP-based systems), sensors, or technical equipment
• Proven ability to work independently in the field with minimal supervision
• Comfortable interacting directly with clients and managing expectations
• Ability to navigate and solve problems in complex, fast-moving environments

Preferred Qualifications

• Experience in industrial, life sciences, or technical field service environments
• Familiarity with IoT systems, automation, or instrumentation
• Strong communication skills with both technical and non-technical stakeholders

Why This Role Stands Out

• High level of autonomy and ownership in the field
• Opportunity to work on complex, real-world technical challenges
• Direct visibility with clients and leadership
• Growth path into lead technician or field leadership roles

Field Technician Jobs Salt Lake City, Senior Field Technician Utah, Field Service Technician, Networking Technician, Installation Technician, Sensor Technician, Technical Field Support, Troubleshooting Technician, IoT Technician, Industrial Field Technician

• Location: Greater Seattle / Pacific Northwest
• Salary: $65-75K + Bonus + Benefits

Are you looking to build a career in validation, commissioning, and qualification (CQV) within the pharmaceutical / life sciences industry? We’re hiring a Validation Engineer / Validation Specialist who wants hands-on experience across IQ, OQ, PQ, exposure to real projects, and a clear path into leadership. This is an opportunity to grow quickly in a GMP-regulated environment, working alongside experienced engineers while taking ownership of meaningful validation work.

What You’ll Do

• Execute and support IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) protocols
• Work on validation of lab systems, equipment, and utilities
• Partner with engineering, validation teams, and lab stakeholders
• Assist with project scheduling, coordination, and resource planning
• Support commissioning & qualification (CQV) activities across projects
• Contribute to GMP / GxP documentation and compliance efforts
• Learn to lead validation workstreams and progress into a Validation Engineer / Project Lead role

What We’re Looking For

• 2+ years of experience in:
  • Validation Engineering
  • CQV (Commissioning, Qualification, Validation)
  • or GMP-regulated environments (Pharma / Biotech)
• Strong understanding of:
  • GMP / GxP / FDA regulations
  • Validation lifecycle (IQ/OQ/PQ)
• Ability to work cross-functionally with engineering, QA, and operations teams
• Strong communication and problem-solving skills
• Coachable, driven, and motivated to grow into leadership

Requirements

• Bachelor’s degree in Engineering, Life Sciences, or related field
• Willingness to travel regionally (project-based work)
• Experience with validation documentation, protocols, and execution

Nice to Have

• Experience with lab systems, utilities, or manufacturing equipment validation
• Exposure to commissioning activities (C&Q / CQV)
• Familiarity with AI tools for validation or documentation

Why This Role

• Hands-on experience across pharma validation projects
• Clear path into senior validation or project leadership roles
• Work alongside experienced engineers in regulated environments
• Real ownership early in your career 

Validation Engineer, Validation Specialist, CQV Engineer, Commissioning Engineer, Qualification Engineer, GMP Validation, GxP, IQ OQ PQ, Pharmaceutical Validation, Life Sciences Validation, Equipment Validation, Utilities Validation, Computer System Validation, CSV Engineer, FDA Compliance, GMP Engineer

• Location: Salt Lake City, Utah (Field-Based)
• Compensation: $65-$85k + bonus + benefits

Are you a seasoned Calibration Technician who thrives in complex environments and knows how to solve problems without waiting for direction?

We’re hiring a Senior Calibration Technician in Salt Lake City, UT to support advanced installations, troubleshooting, and client-facing technical work. This is a high-impact role for someone who can step into the field, assess issues quickly, and deliver solutions with confidence.

If you have strong experience with networking, sensors, or technical systems, and you’re comfortable owning projects independently, this is built for you.

What You’ll Do

• Lead installation, configuration, and maintenance of technical systems in the field
• Troubleshoot complex networking, sensor, and system-level issues in real-time
• Serve as the on-site technical expert for clients and internal stakeholders
• Handle escalations and resolve high-priority technical challenges
• Work independently to assess environments, identify risks, and implement solutions
• Document field activity, system performance, and resolutions clearly

What We’re Looking For

• 5+ years of experience as a Field Technician, Field Service Technician, or similar role
• Strong background in troubleshooting, installation, and system diagnostics
• Experience with networking (IP-based systems), sensors, or technical equipment
• Proven ability to work independently in the field with minimal supervision
• Comfortable interacting directly with clients and managing expectations
• Ability to navigate and solve problems in complex, fast-moving environments

Preferred Qualifications

• Experience in industrial, life sciences, or technical field service environments
• Familiarity with IoT systems, automation, or instrumentation
• Strong communication skills with both technical and non-technical stakeholders

Why This Role Stands Out

• High level of autonomy and ownership in the field
• Opportunity to work on complex, real-world technical challenges
• Direct visibility with clients and leadership
• Growth path into lead technician or field leadership roles

Field Technician Jobs Salt Lake City, Senior Field Technician Utah, Field Service Technician, Networking Technician, Installation Technician, Sensor Technician, Technical Field Support, Troubleshooting Technician, IoT Technician, Industrial Field Technician

Calibration, Validation, Field Service, GMP, Life Sciences

We’re hiring a Field Quality & Validation Lead to drive quality, compliance, and execution across field service operations in the West Region. This is a hands-on leadership role focused on first-pass success, eliminating rework, and hitting turnaround targets.

Key Responsibilities

• Lead field quality oversight for calibration & validation services
• Ensure 7-day turnaround on field jobs
• Drive first-pass success and eliminate repeat visits
• Coach and develop field technicians
• Write/review IQ/OQ/PQ validation protocols
• Lead deviation investigations, root cause analysis, CAPA
• Review calibration certificates & quality documentation
• Manage client escalations and technical issues
• Ensure GMP compliance and audit readiness

Requirements

• Experience in calibration, validation, or field service (life sciences/GMP)
• Strong knowledge of IQ/OQ/PQ, deviations, CAPA
• Ability to lead technicians and improve field performance
• Experience with GMP compliance and documentation

Why Join

• High-impact, field-facing leadership role
• Opportunity to own quality and drive real operational change
• Work with top life sciences clients and technologies

Calibration, Validation Engineer, Validation Specialist, Field Service, GMP, IQ OQ PQ, Commissioning, Metrology, CAPA, Deviation, Pharmaceutical, Biotech, Quality Assurance, Field Technician, Compliance

• Location: Maryland/DC
• Salary: $70-100K + Bonus + Benefits

Are you looking to build a career in validation, commissioning, and qualification (CQV) within the pharmaceutical / life sciences industry? We’re hiring a Validation Engineer / Validation Specialist who wants hands-on experience across IQ, OQ, PQ, exposure to real projects, and a clear path into leadership. This is an opportunity to grow quickly in a GMP-regulated environment, working alongside experienced engineers while taking ownership of meaningful validation work.

What You’ll Do

• Execute and support IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) protocols
• Work on validation of lab systems, equipment, and utilities
• Partner with engineering, validation teams, and lab stakeholders
• Assist with project scheduling, coordination, and resource planning
• Support commissioning & qualification (CQV) activities across projects
• Contribute to GMP / GxP documentation and compliance efforts
• Learn to lead validation workstreams and progress into a Validation Engineer / Project Lead role

What We’re Looking For

• 2+ years of experience in:
  • Validation Engineering
  • CQV (Commissioning, Qualification, Validation)
  • or GMP-regulated environments (Pharma / Biotech)
• Strong understanding of:
  • GMP / GxP / FDA regulations
  • Validation lifecycle (IQ/OQ/PQ)
• Ability to work cross-functionally with engineering, QA, and operations teams
• Strong communication and problem-solving skills
• Coachable, driven, and motivated to grow into leadership

Requirements

• Bachelor’s degree in Engineering, Life Sciences, or related field
• Willingness to travel regionally (project-based work)
• Experience with validation documentation, protocols, and execution

Nice to Have

• Experience with lab systems, utilities, or manufacturing equipment validation
• Exposure to commissioning activities (C&Q / CQV)
• Familiarity with AI tools for validation or documentation

Why This Role

• Hands-on experience across pharma validation projects
• Clear path into senior validation or project leadership roles
• Work alongside experienced engineers in regulated environments
• Real ownership early in your career 

Validation Engineer, Validation Specialist, CQV Engineer, Commissioning Engineer, Qualification Engineer, GMP Validation, GxP, IQ OQ PQ, Pharmaceutical Validation, Life Sciences Validation, Equipment Validation, Utilities Validation, Computer System Validation, CSV Engineer, FDA Compliance, GMP Engineer

• Location: Maryland/DC
• Salary: $70-100K + Bonus + Benefits

Are you looking to build a career in validation, commissioning, and qualification (CQV) within the pharmaceutical / life sciences industry? We’re hiring a Validation Engineer / Validation Specialist who wants hands-on experience across IQ, OQ, PQ, exposure to real projects, and a clear path into leadership. This is an opportunity to grow quickly in a GMP-regulated environment, working alongside experienced engineers while taking ownership of meaningful validation work.

What You’ll Do

• Execute and support IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) protocols
• Work on validation of lab systems, equipment, and utilities
• Partner with engineering, validation teams, and lab stakeholders
• Assist with project scheduling, coordination, and resource planning
• Support commissioning & qualification (CQV) activities across projects
• Contribute to GMP / GxP documentation and compliance efforts
• Learn to lead validation workstreams and progress into a Validation Engineer / Project Lead role

What We’re Looking For

• 2+ years of experience in:
  • Validation Engineering
  • CQV (Commissioning, Qualification, Validation)
  • or GMP-regulated environments (Pharma / Biotech)
• Strong understanding of:
  • GMP / GxP / FDA regulations
  • Validation lifecycle (IQ/OQ/PQ)
• Ability to work cross-functionally with engineering, QA, and operations teams
• Strong communication and problem-solving skills
• Coachable, driven, and motivated to grow into leadership

Requirements

• Bachelor’s degree in Engineering, Life Sciences, or related field
• Willingness to travel regionally (project-based work)
• Experience with validation documentation, protocols, and execution

Nice to Have

• Experience with lab systems, utilities, or manufacturing equipment validation
• Exposure to commissioning activities (C&Q / CQV)
• Familiarity with AI tools for validation or documentation

Why This Role

• Hands-on experience across pharma validation projects
• Clear path into senior validation or project leadership roles
• Work alongside experienced engineers in regulated environments
• Real ownership early in your career 

Validation Engineer, Validation Specialist, CQV Engineer, Commissioning Engineer, Qualification Engineer, GMP Validation, GxP, IQ OQ PQ, Pharmaceutical Validation, Life Sciences Validation, Equipment Validation, Utilities Validation, Computer System Validation, CSV Engineer, FDA Compliance, GMP Engineer

• Location: New York City
• Salary: $70-100K + Bonus + Benefits

Are you looking to build a career in validation, commissioning, and qualification (CQV) within the pharmaceutical / life sciences industry? We’re hiring a Validation Engineer / Validation Specialist who wants hands-on experience across IQ, OQ, PQ, exposure to real projects, and a clear path into leadership. This is an opportunity to grow quickly in a GMP-regulated environment, working alongside experienced engineers while taking ownership of meaningful validation work.

What You’ll Do

• Execute and support IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) protocols
• Work on validation of lab systems, equipment, and utilities
• Partner with engineering, validation teams, and lab stakeholders
• Assist with project scheduling, coordination, and resource planning
• Support commissioning & qualification (CQV) activities across projects
• Contribute to GMP / GxP documentation and compliance efforts
• Learn to lead validation workstreams and progress into a Validation Engineer / Project Lead role

What We’re Looking For

• 2+ years of experience in:
  • Validation Engineering
  • CQV (Commissioning, Qualification, Validation)
  • or GMP-regulated environments (Pharma / Biotech)
• Strong understanding of:
  • GMP / GxP / FDA regulations
  • Validation lifecycle (IQ/OQ/PQ)
• Ability to work cross-functionally with engineering, QA, and operations teams
• Strong communication and problem-solving skills
• Coachable, driven, and motivated to grow into leadership

Requirements

• Bachelor’s degree in Engineering, Life Sciences, or related field
• Willingness to travel regionally (project-based work)
• Experience with validation documentation, protocols, and execution

Nice to Have

• Experience with lab systems, utilities, or manufacturing equipment validation
• Exposure to commissioning activities (C&Q / CQV)
• Familiarity with AI tools for validation or documentation

Why This Role

• Hands-on experience across pharma validation projects
• Clear path into senior validation or project leadership roles
• Work alongside experienced engineers in regulated environments
• Real ownership early in your career 

Validation Engineer, Validation Specialist, CQV Engineer, Commissioning Engineer, Qualification Engineer, GMP Validation, GxP, IQ OQ PQ, Pharmaceutical Validation, Life Sciences Validation, Equipment Validation, Utilities Validation, Computer System Validation, CSV Engineer, FDA Compliance, GMP Engineer

• Location: Greater Chicago
• Salary: $70-100K + Bonus + Benefits
• No Sponsorship, No Relocation

Are you looking to build a career in validation, commissioning, and qualification (CQV) within the pharmaceutical / life sciences industry? We’re hiring a Validation Engineer who wants hands-on experience across IQ, OQ, PQ, exposure to real projects, and a clear path into leadership. This is an opportunity to grow quickly in a GMP-regulated environment, working alongside experienced engineers while taking ownership of meaningful validation work.

What You’ll Do

• Execute and support IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) protocols
• Work on validation of lab systems, equipment, and utilities
• Partner with engineering, validation teams, and lab stakeholders
• Assist with project scheduling, coordination, and resource planning
• Support commissioning & qualification (CQV) activities across projects
• Contribute to GMP / GxP documentation and compliance efforts
• Learn to lead validation workstreams and progress into a Validation Project Lead role

What We’re Looking For

• 5+ years of experience in:
  • Validation Engineering
  • CQV (Commissioning, Qualification, Validation)
  • or GMP-regulated environments (Pharma / Biotech)
• Strong understanding of:
  • GMP / GxP / FDA regulations
  • Validation lifecycle (IQ/OQ/PQ)
• Ability to work cross-functionally with engineering, QA, and operations teams
• Strong communication and problem-solving skills
• Coachable, driven, and motivated to grow into leadership

Requirements

• Bachelor’s degree in Engineering, Life Sciences, or related field
• Willingness to travel regionally (project-based work)
• Experience with validation documentation, protocols, and execution

Nice to Have

• Experience with lab systems, utilities, or manufacturing equipment validation
• Exposure to commissioning activities (C&Q / CQV)
• Familiarity with AI tools for validation or documentation

Why This Role

• Hands-on experience across pharma validation projects
• Clear path into senior validation or project leadership roles
• Work alongside experienced engineers in regulated environments

Validation Engineer, Validation Specialist, CQV Engineer, Commissioning Engineer, Qualification Engineer, GMP Validation, GxP, IQ OQ PQ, Pharmaceutical Validation, Life Sciences Validation, Equipment Validation, Utilities Validation, Computer System Validation, CSV Engineer, FDA Compliance, GMP Engineer

• Location: Northern California, SF, Sacramento, SJ
• Salary: $70-100K + Bonus + Benefits

Are you looking to build a career in validation, commissioning, and qualification (CQV) within the pharmaceutical / life sciences industry? We’re hiring a Validation Engineer / Validation Specialist who wants hands-on experience across IQ, OQ, PQ, exposure to real projects, and a clear path into leadership. This is an opportunity to grow quickly in a GMP-regulated environment, working alongside experienced engineers while taking ownership of meaningful validation work.

What You’ll Do

• Execute and support IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) protocols
• Work on validation of lab systems, equipment, and utilities
• Partner with engineering, validation teams, and lab stakeholders
• Assist with project scheduling, coordination, and resource planning
• Support commissioning & qualification (CQV) activities across projects
• Contribute to GMP / GxP documentation and compliance efforts
• Learn to lead validation workstreams and progress into a Validation Engineer / Project Lead role

What We’re Looking For

• 2+ years of experience in:
  • Validation Engineering
  • CQV (Commissioning, Qualification, Validation)
  • or GMP-regulated environments (Pharma / Biotech)
• Strong understanding of:
  • GMP / GxP / FDA regulations
  • Validation lifecycle (IQ/OQ/PQ)
• Ability to work cross-functionally with engineering, QA, and operations teams
• Strong communication and problem-solving skills
• Coachable, driven, and motivated to grow into leadership

Requirements

• Bachelor’s degree in Engineering, Life Sciences, or related field
• Willingness to travel regionally (project-based work)
• Experience with validation documentation, protocols, and execution

Nice to Have

• Experience with lab systems, utilities, or manufacturing equipment validation
• Exposure to commissioning activities (C&Q / CQV)
• Familiarity with AI tools for validation or documentation

Why This Role

• Hands-on experience across pharma validation projects
• Clear path into senior validation or project leadership roles
• Work alongside experienced engineers in regulated environments
• Real ownership early in your career 

Validation Engineer, Validation Specialist, CQV Engineer, Commissioning Engineer, Qualification Engineer, GMP Validation, GxP, IQ OQ PQ, Pharmaceutical Validation, Life Sciences Validation, Equipment Validation, Utilities Validation, Computer System Validation, CSV Engineer, FDA Compliance, GMP Engineer

• Location: Northern California, SF, Sacramento, SJ
• Salary: $70-100K + Bonus + Benefits

Are you looking to build a career in validation, commissioning, and qualification (CQV) within the pharmaceutical / life sciences industry? We’re hiring a Validation Engineer / Validation Specialist who wants hands-on experience across IQ, OQ, PQ, exposure to real projects, and a clear path into leadership. This is an opportunity to grow quickly in a GMP-regulated environment, working alongside experienced engineers while taking ownership of meaningful validation work.

What You’ll Do

• Execute and support IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) protocols
• Work on validation of lab systems, equipment, and utilities
• Partner with engineering, validation teams, and lab stakeholders
• Assist with project scheduling, coordination, and resource planning
• Support commissioning & qualification (CQV) activities across projects
• Contribute to GMP / GxP documentation and compliance efforts
• Learn to lead validation workstreams and progress into a Validation Engineer / Project Lead role

What We’re Looking For

• 2+ years of experience in:
  • Validation Engineering
  • CQV (Commissioning, Qualification, Validation)
  • or GMP-regulated environments (Pharma / Biotech)
• Strong understanding of:
  • GMP / GxP / FDA regulations
  • Validation lifecycle (IQ/OQ/PQ)
• Ability to work cross-functionally with engineering, QA, and operations teams
• Strong communication and problem-solving skills
• Coachable, driven, and motivated to grow into leadership

Requirements

• Bachelor’s degree in Engineering, Life Sciences, or related field
• Willingness to travel regionally (project-based work)
• Experience with validation documentation, protocols, and execution

Nice to Have

• Experience with lab systems, utilities, or manufacturing equipment validation
• Exposure to commissioning activities (C&Q / CQV)
• Familiarity with AI tools for validation or documentation

Why This Role

• Hands-on experience across pharma validation projects
• Clear path into senior validation or project leadership roles
• Work alongside experienced engineers in regulated environments
• Real ownership early in your career 

Validation Engineer, Validation Specialist, CQV Engineer, Commissioning Engineer, Qualification Engineer, GMP Validation, GxP, IQ OQ PQ, Pharmaceutical Validation, Life Sciences Validation, Equipment Validation, Utilities Validation, Computer System Validation, CSV Engineer, FDA Compliance, GMP Engineer

• Greater Philadelphia / Southern New Jersey (Hybrid)
• Salary: 50-60k + benefits

We’re looking for a Scheduler / Scheduling Coordinator who can keep projects moving by putting the right people on the right work at the right time. This role sits at the center of operations partnering with leadership and project teams to coordinate internal resources, manage utilization, and solve scheduling challenges in real time. This is not about years of experience. It’s about your ability to stay organized, think clearly under pressure, build relationships, and make things happen.

What You’ll Do

• Coordinate and manage project schedules and resource allocation across multiple teams
• Partner with leadership to align staffing needs with project demand
• Optimize utilization and resource planning across internal teams
• Act as the central point of coordination between project managers, team members, and leadership
• Identify scheduling conflicts and troubleshoot in real time
• Communicate updates, risks, and changes clearly to stakeholders
• Escalate issues when needed to keep projects on track
• Maintain scheduling systems, trackers, and reporting

What We’re Looking For

• Experience in scheduling, coordination, project support, or operations
• Strong ability to manage multiple priorities and timelines simultaneously
• Proven ability to build relationships and communicate across teams
• Comfortable working in a fast-paced, dynamic environment
• Ability to stay calm under pressure and solve problems quickly
• Strong organizational and attention-to-detail skills
• Experience with resource planning, utilization tracking, or workforce coordination is a plus

Why This Role

• High visibility across leadership and project teams
• Direct impact on project success and team performance
• Opportunity to grow into operations, project management, or resource management
• Fast-moving environment where your work actually matters 

Scheduler, Scheduling Coordinator, Project Coordinator, Resource Coordinator, Resource Planner, Workforce Planner, Staffing Coordinator, Operations Coordinator, Project Scheduling, Resource Planning, Utilization Management, Capacity Planning, Workforce Scheduling, Project Support

• Greater Philadelphia / Southern New Jersey (Hybrid)
  Salary: 50-60k + benefits

We’re looking for a Scheduler / Scheduling Coordinator who can keep projects moving by putting the right people on the right work at the right time. This role sits at the center of operations partnering with leadership and project teams to coordinate internal resources, manage utilization, and solve scheduling challenges in real time. This is not about years of experience. It’s about your ability to stay organized, think clearly under pressure, build relationships, and make things happen.

What You’ll Do

• Coordinate and manage project schedules and resource allocation across multiple teams
• Partner with leadership to align staffing needs with project demand
• Optimize utilization and resource planning across internal teams
• Act as the central point of coordination between project managers, team members, and leadership
• Identify scheduling conflicts and troubleshoot in real time
• Communicate updates, risks, and changes clearly to stakeholders
• Escalate issues when needed to keep projects on track
• Maintain scheduling systems, trackers, and reporting

What We’re Looking For

• Experience in scheduling, coordination, project support, or operations
• Strong ability to manage multiple priorities and timelines simultaneously
• Proven ability to build relationships and communicate across teams
• Comfortable working in a fast-paced, dynamic environment
• Ability to stay calm under pressure and solve problems quickly
• Strong organizational and attention-to-detail skills
• Experience with resource planning, utilization tracking, or workforce coordination is a plus

Why This Role

• High visibility across leadership and project teams
• Direct impact on project success and team performance
• Opportunity to grow into operations, project management, or resource management
• Fast-moving environment where your work actually matters 

Scheduler, Scheduling Coordinator, Project Coordinator, Resource Coordinator, Resource Planner, Workforce Planner, Staffing Coordinator, Operations Coordinator, Project Scheduling, Resource Planning, Utilization Management, Capacity Planning, Workforce Scheduling, Project Support

• Location: Southern NJ / Greater Philadelphia
• Hybrid: 3 days on-site & 2 days remote
• Salary: $75,000 – $85,000 + bonus + benefits

We’re looking for a Project Manager who knows how to move work forward across teams, manage client relationships, and keep projects on track—without overcomplicating it. This is a hands-on role where you’ll lead cross-functional projects, work directly with customers, and manage timelines, KPIs, and budgets in a fast-paced environment. If you’ve operated in life sciences, GMP environments, or IT implementation projects, you’ll stand out immediately.

What You’ll Do

• Own project timelines, deliverables, and execution from kickoff through completion
• Manage client relationships, ensuring clear communication and strong delivery
• Track and report on KPIs, milestones, and financial budgets
• Drive alignment across stakeholders to keep projects moving forward
• Support IT/networking or system implementation projects where applicable

What We’re Looking For

• 3+ years of experience as a Project Manager
• Proven experience managing cross-functional teams and multiple stakeholders
• Strong background in customer-facing project management
• Experience tracking KPIs, budgets, and project performance metrics
• Exposure to one or more of the following:
  • Life Sciences / Pharmaceutical environments
  • GMP-regulated environments
  • IT networking or system implementations
• Strong communication and organizational skills

Why This Role

• Clear ownership and visibility across projects
• Direct interaction with internal & external clients and leadership
• Opportunity to grow within project management and operations
• Stable environment with consistent project flow

Project Manager, IT Project Manager, Technical Project Manager, Life Sciences Project Manager, GMP Project Manager, Pharmaceutical Project Manager, Validation Project Manager, Implementation Project Manager, Cross-functional Project Manager, Client-facing Project Manager, KPI Management, Budget Management, Stakeholder Management

• Location: Southern NJ / Greater Philadelphia
• Hybrid: 3 days on-site & 2 days remote
• Salary: $75,000 – $85,000 + bonus + benefits

We’re looking for a Project Manager who knows how to move work forward across teams, manage client relationships, and keep projects on track—without overcomplicating it. This is a hands-on role where you’ll lead cross-functional projects, work directly with customers, and manage timelines, KPIs, and budgets in a fast-paced environment. If you’ve operated in life sciences, GMP environments, or IT implementation projects, you’ll stand out immediately.

What You’ll Do

• Own project timelines, deliverables, and execution from kickoff through completion
• Manage client relationships, ensuring clear communication and strong delivery
• Track and report on KPIs, milestones, and financial budgets
• Drive alignment across stakeholders to keep projects moving forward
• Support IT/networking or system implementation projects where applicable

What We’re Looking For

• 3+ years of experience as a Project Manager
• Proven experience managing cross-functional teams and multiple stakeholders
• Strong background in customer-facing project management
• Experience tracking KPIs, budgets, and project performance metrics
• Exposure to one or more of the following:
  • Life Sciences / Pharmaceutical environments
  • GMP-regulated environments
  • IT networking or system implementations
• Strong communication and organizational skills

Why This Role

• Clear ownership and visibility across projects
• Direct interaction with internal & external clients and leadership
• Opportunity to grow within project management and operations
• Stable environment with consistent project flow

Project Manager, IT Project Manager, Technical Project Manager, Life Sciences Project Manager, GMP Project Manager, Pharmaceutical Project Manager, Validation Project Manager, Implementation Project Manager, Cross-functional Project Manager, Client-facing Project Manager, KPI Management, Budget Management, Stakeholder Management

• Location: Southern NJ / Greater Philadelphia
• Hybrid: 3 days on-site & 2 days remote
• Salary: $75,000 – $85,000 + bonus + benefits

We’re looking for a Project Manager who knows how to move work forward across teams, manage client relationships, and keep projects on track—without overcomplicating it. This is a hands-on role where you’ll lead cross-functional projects, work directly with customers, and manage timelines, KPIs, and budgets in a fast-paced environment. If you’ve operated in life sciences, GMP environments, or IT implementation projects, you’ll stand out immediately.

What You’ll Do

• Own project timelines, deliverables, and execution from kickoff through completion
• Manage client relationships, ensuring clear communication and strong delivery
• Track and report on KPIs, milestones, and financial budgets
• Drive alignment across stakeholders to keep projects moving forward
• Support IT/networking or system implementation projects where applicable

What We’re Looking For

• 3+ years of experience as a Project Manager
• Proven experience managing cross-functional teams and multiple stakeholders
• Strong background in customer-facing project management
• Experience tracking KPIs, budgets, and project performance metrics
• Exposure to one or more of the following:
  • Life Sciences / Pharmaceutical environments
  • GMP-regulated environments
  • IT networking or system implementations
• Strong communication and organizational skills

Why This Role

• Clear ownership and visibility across projects
• Direct interaction with internal & external clients and leadership
• Opportunity to grow within project management and operations
• Stable environment with consistent project flow

Project Manager, IT Project Manager, Technical Project Manager, Life Sciences Project Manager, GMP Project Manager, Pharmaceutical Project Manager, Validation Project Manager, Implementation Project Manager, Cross-functional Project Manager, Client-facing Project Manager, KPI Management, Budget Management, Stakeholder Management

Are you hungry to learn, grow, and own your career in pharmaceutical validation? We’re looking for a Validation Engineer / Specialist who wants hands-on experience and a clear path to leadership.

What You’ll Do

• Support IQ, OQ, PQ protocols for lab systems, equipment, and utilities
• Partner with lab teams, engineers, and managers to understand systems
• Assist with project scheduling, resource planning, and field coordination
• Learn on the job, then grow into leading validation activities

Who You Are

• Coachable, energetic, and hungry for growth
• Solutions-oriented, analytical, and accountable
• Comfortable starting as a follower, then stepping into leadership
• First in, last out, committed to results
• Strong communicator with technical fluency

Requirements

• Bachelor’s in Engineering, Life Sciences, or related field
• 2+ years in validation, CQV, commissioning, or regulated environments
• Knowledge of GMP, GxP, FDA compliance
• Willingness to travel regionally

Bonus: Exposure to IQ/OQ/PQ execution, lab systems, or AI tools for validation/documentation

Why This Role Rocks

• Hands-on experience with regulated pharma systems
• Clear path to project and team leadership
• Learn from senior engineers while owning real responsibility

Are you hungry to learn, grow, and own your career in pharmaceutical validation? We’re looking for a Validation Engineer / Specialist who wants hands-on experience, regional travel, and a clear path to leadership.

What You’ll Do

• Support IQ, OQ, PQ protocols for lab systems, equipment, and utilities
• Partner with lab teams, engineers, and managers to understand systems
• Assist with project scheduling, resource planning, and field coordination
• Learn on the job, then grow into leading validation activities

Who You Are

• Coachable, energetic, and hungry for growth
• Solutions-oriented, analytical, and accountable
• Comfortable starting as a follower, then stepping into leadership
• First in, last out, committed to results
• Strong communicator with technical fluency

Requirements

• Bachelor’s in Engineering, Life Sciences, or related field
• 2+ years in validation, CQV, commissioning, or regulated environments
• Knowledge of GMP, GxP, FDA compliance
• Willingness to travel regionally

Bonus: Exposure to IQ/OQ/PQ execution, lab systems, or AI tools for validation/documentation

Why This Role Rocks

• Hands-on experience with regulated pharma systems
• Clear path to project and team leadership
• Learn from senior engineers while owning real responsibility

Are you hungry to learn, grow, and own your career in pharmaceutical validation? We’re looking for a Validation Engineer / Specialist who wants hands-on experience, regional travel, and a clear path to leadership.

What You’ll Do

• Support IQ, OQ, PQ protocols for lab systems, equipment, and utilities
• Partner with lab teams, engineers, and managers to understand systems
• Assist with project scheduling, resource planning, and field coordination
• Learn on the job, then grow into leading validation activities

Who You Are

• Coachable, energetic, and hungry for growth
• Solutions-oriented, analytical, and accountable
• Comfortable starting as a follower, then stepping into leadership
• First in, last out, committed to results
• Strong communicator with technical fluency

Requirements

• Bachelor’s in Engineering, Life Sciences, or related field
• 2+ years in validation, CQV, commissioning, or regulated environments
• Knowledge of GMP, GxP, FDA compliance
• Willingness to travel regionally

Bonus: Exposure to IQ/OQ/PQ execution, lab systems, or AI tools for validation/documentation

Why This Role Rocks

• Hands-on experience with regulated pharma systems
• Clear path to project and team leadership
• Learn from senior engineers while owning real responsibility