Overview
On Site
Full Time
Skills
Biomedical Engineering
Pharmaceutics
HATS
Continuous Improvement
Maintenance Planning
Brand
Apache Flex
Sustainability
Reporting
Engineering Support
Startups
Business Cases
Reliability Engineering
EHS
Root Cause Analysis
Data Analysis
Technical Support
Process Control
Process Engineering
Leadership
SAP BASIS
Instrumentation
Expect
Adaptability
Mechanical Engineering
Manufacturing
Good Manufacturing Practice
Quality Management
Change Control
Corrective And Preventive Action
Communication
Technical Writing
Presentations
Collaboration
Facilitation
Analytical Skill
Process Improvement
Project Implementation
Procurement
GMP
Regulatory Compliance
Management
Multitasking
Manufacturing Operations
Job Details
Onsite: Client North Carolina (Holly Springs) - Relo candidates can be considered
Duration: 3-year contract
Openings: 3
Standard business hours (~8 to 5) with flexibility for: Evening or weekend work, Occasional holiday support, Up to ~50 hours/week, assuming occasional OT
Department: ANC Engineering
Ideal candidate is a commercially experienced Process Engineer with a BS in Chemical, Mechanical, or Biomedical Engineering, who has supported large-scale drug substance operations in biotech or pharma. They are hands-on with equipment ownership (not maintenance) and are highly adaptable, collaborative, and proactive. The ideal candidate embraces ambiguity, is passionate about solving complex operational problems, and thrives in a startup-like GMP environment where they can wear multiple hats, support dynamic business needs, and help drive continuous improvement initiatives. Recruiters expected to pre-screen thoroughly and look for tangible examples of initiative and project ownership. Ideal resumes will show practical accomplishments and clearly demonstrate team-based, cross-functional efforts
Not a maintenance role: They design/own the equipment and support proper maintenance planning, not execution.
This opportunity is based at a brand-new, advanced biologics manufacturing plant. The site features a cutting-edge FleX Batch facility that combines the latest in disposable technologies with traditional stainless-steel systems, enabling maximum operational flexibility. The facility integrates best-in-class manufacturing processes and industry 4.0 capabilities, along with sustainability initiatives designed to reduce carbon emissions and waste.
Process Engineer
Live
What you will do
In this role, the Engineer will report to the Senior Manager of the Process Engineering group and will provide daily engineering support to the site. Responsibilities include:
Serve as system owner for process equipment and systems supporting manufacturing operations.
Provide engineering support for design, construction, startup, commissioning, and qualification of new or modified systems.
Identify and/or lead implementation of small-to-medium scale equipment or facility improvements, including development of business cases.
Develop maintenance programs, ensure spare part availability, and coordinate execution to maintain system reliability.
Ensure systems operate safely and in compliance with EHS standards and regulations.
Support commissioning and qualification activities in alignment with GMP requirements and regulatory inspections.
Apply engineering principles in daily operations, maintenance, and troubleshooting of plant systems.
Monitor system performance and implement risk-reduction strategies.
Lead or support troubleshooting efforts to minimize production downtime, including root cause analysis and CAPA implementation.
Support new product and technology introductions via engineering assessments, equipment modifications, and pilot runs.
Advance use of predictive maintenance and condition-based monitoring using data analytics where applicable.
Lead or contribute to deviation investigations and other quality-related processes.
Analyze and present findings related to operational issues and engineering projects.
Provide technical support to commercial and clinical manufacturing, specifically in process control and equipment.
Collaborate with cross-functional groups such as manufacturing, process development, utilities, maintenance, quality, and validation to drive operational improvements.
Maintain regular communication with leadership and team members, escalating issues with proposed solutions.
Participate in a small engineering team on a project or ongoing support basis.
Provide rotational on-call support for utility systems, including nights, weekends, and holidays as needed.
Participate in the design and selection of systems, instrumentation, and components.
Evaluate supplier capabilities and assess new technologies to improve cost, throughput, or technical capabilities.
Win
What we expect of you
We value diverse perspectives and contributions. The engineering professional we seek is dynamic, adaptable, and team-oriented, with the following qualifications:
Preferred Qualifications:
Bachelor's degree in Chemical or Mechanical Engineering.
6+ years of relevant work experience, including 5+ years in a biopharmaceutical manufacturing environment.
Hands-on experience with GMP production equipment such as bioreactors, centrifuges, filtration systems, and purification technologies.
Proficiency with equipment and facility control systems, including troubleshooting and logic understanding.
Experience in regulated environments (e.g., cGMP, OSHA, EPA) and knowledge of quality systems (e.g., change control, non-conformances, CAPA, validation).
Strong communication, technical writing, and presentation skills; ability to work independently.
Proven team collaboration and facilitation skills.
Analytical thinking with the ability to interpret complex problems using multiple data sources.
Ability to support capital projects and implement process improvements.
Understanding of capital project execution from procurement through validation in GMP environments.
Commitment to safety and compliance in all engineering activities.
Self-starter with excellent organization, time management, and multitasking skills.
Willingness to work flexible hours in support of 24/7 manufacturing operations.
Duration: 3-year contract
Openings: 3
Standard business hours (~8 to 5) with flexibility for: Evening or weekend work, Occasional holiday support, Up to ~50 hours/week, assuming occasional OT
Department: ANC Engineering
Ideal candidate is a commercially experienced Process Engineer with a BS in Chemical, Mechanical, or Biomedical Engineering, who has supported large-scale drug substance operations in biotech or pharma. They are hands-on with equipment ownership (not maintenance) and are highly adaptable, collaborative, and proactive. The ideal candidate embraces ambiguity, is passionate about solving complex operational problems, and thrives in a startup-like GMP environment where they can wear multiple hats, support dynamic business needs, and help drive continuous improvement initiatives. Recruiters expected to pre-screen thoroughly and look for tangible examples of initiative and project ownership. Ideal resumes will show practical accomplishments and clearly demonstrate team-based, cross-functional efforts
Not a maintenance role: They design/own the equipment and support proper maintenance planning, not execution.
This opportunity is based at a brand-new, advanced biologics manufacturing plant. The site features a cutting-edge FleX Batch facility that combines the latest in disposable technologies with traditional stainless-steel systems, enabling maximum operational flexibility. The facility integrates best-in-class manufacturing processes and industry 4.0 capabilities, along with sustainability initiatives designed to reduce carbon emissions and waste.
Process Engineer
Live
What you will do
In this role, the Engineer will report to the Senior Manager of the Process Engineering group and will provide daily engineering support to the site. Responsibilities include:
Serve as system owner for process equipment and systems supporting manufacturing operations.
Provide engineering support for design, construction, startup, commissioning, and qualification of new or modified systems.
Identify and/or lead implementation of small-to-medium scale equipment or facility improvements, including development of business cases.
Develop maintenance programs, ensure spare part availability, and coordinate execution to maintain system reliability.
Ensure systems operate safely and in compliance with EHS standards and regulations.
Support commissioning and qualification activities in alignment with GMP requirements and regulatory inspections.
Apply engineering principles in daily operations, maintenance, and troubleshooting of plant systems.
Monitor system performance and implement risk-reduction strategies.
Lead or support troubleshooting efforts to minimize production downtime, including root cause analysis and CAPA implementation.
Support new product and technology introductions via engineering assessments, equipment modifications, and pilot runs.
Advance use of predictive maintenance and condition-based monitoring using data analytics where applicable.
Lead or contribute to deviation investigations and other quality-related processes.
Analyze and present findings related to operational issues and engineering projects.
Provide technical support to commercial and clinical manufacturing, specifically in process control and equipment.
Collaborate with cross-functional groups such as manufacturing, process development, utilities, maintenance, quality, and validation to drive operational improvements.
Maintain regular communication with leadership and team members, escalating issues with proposed solutions.
Participate in a small engineering team on a project or ongoing support basis.
Provide rotational on-call support for utility systems, including nights, weekends, and holidays as needed.
Participate in the design and selection of systems, instrumentation, and components.
Evaluate supplier capabilities and assess new technologies to improve cost, throughput, or technical capabilities.
Win
What we expect of you
We value diverse perspectives and contributions. The engineering professional we seek is dynamic, adaptable, and team-oriented, with the following qualifications:
Preferred Qualifications:
Bachelor's degree in Chemical or Mechanical Engineering.
6+ years of relevant work experience, including 5+ years in a biopharmaceutical manufacturing environment.
Hands-on experience with GMP production equipment such as bioreactors, centrifuges, filtration systems, and purification technologies.
Proficiency with equipment and facility control systems, including troubleshooting and logic understanding.
Experience in regulated environments (e.g., cGMP, OSHA, EPA) and knowledge of quality systems (e.g., change control, non-conformances, CAPA, validation).
Strong communication, technical writing, and presentation skills; ability to work independently.
Proven team collaboration and facilitation skills.
Analytical thinking with the ability to interpret complex problems using multiple data sources.
Ability to support capital projects and implement process improvements.
Understanding of capital project execution from procurement through validation in GMP environments.
Commitment to safety and compliance in all engineering activities.
Self-starter with excellent organization, time management, and multitasking skills.
Willingness to work flexible hours in support of 24/7 manufacturing operations.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.