Process Engineer | Medical Equipment or Pharma Manufacturing

Phoenix VX; Albany (GA); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Medical premiums

401k match

Tuition reimbursement

Job summary

Phoenix VX on site in Albany, GA seeks a Process Engineer/Manufacturing Engineer/Validation Engineer to own and drive manufacturing processes from validation through continuous improvement. You’ll tackle complex production challenges, write critical documents, and work across Engineering, Quality, and Operations to optimize performance.

Strong background in validation (IQ/OQ/PQ), process troubleshooting, and technical writing is required, with familiarity in GMP-regulated medical device

Qualifications

• 3–5+ years in Medical Device and/or Pharmaceutical manufacturing.
• Engineering, Science, Technology, or closely related technical discipline.
• Demonstrated process and/or equipment validation experience.
• Strong technical writing capabilities.
• Knowledge of U.S. FDA and/or EU MDR medical device regulations.
• Experience in GMP-regulated manufacturing.
• Proven troubleshooting, analytical and problem-solving skills.

Responsibilities

• Lead and support IQ/OQ/PQ process and equipment validation.
• Troubleshoot complex manufacturing and production issues.
• Author qualification documents, validation documentation, SOPs, and technical reports.
• Analyze process data to identify risk, inefficiencies, yield improvements, and CSP opportunities.
• Support new product launches and technology transfers.
• Optimize existing commercial manufacturing processes.
• Lead technical projects from investigation through implementation.
• Partner with Operations, Engineering, Quality, Procurement, and Operational Excellence.
• Support equipment/process qualification and continued process verification.
• Contribute to Lean, Six Sigma, and continuous improvement initiatives.

Skills

IQ/OQ/PQ validation

Troubleshooting

Technical writing

GMP compliance

FDA/EU MDR knowledge

Lean Six Sigma

Education

Engineering/Science/Technology degree

Job description

If you’re a Process Engineer, Manufacturing Engineer, Validation Engineer, or Technical Services professional who likes solving problems where they actually happen—on the manufacturing floor, this may be the opportunity for you.

This role combines process engineering, validation, technical problem-solving, technology transfer, and continuous improvement within a regulated medical device manufacturing environment. You’ll have the opportunity to take ownership of technical projects, improve established manufacturing processes, troubleshoot production challenges, and work cross-functionally with Engineering, Quality, Operations, and other site teams.

WHAT YOU'LL BE DOING

• Lead and support IQ/OQ/PQ process and equipment validation
• Troubleshoot complex manufacturing and production issues
• Author qualification documents, validation documentation, SOPs, and technical reports
• Analyze process data to identify risk, inefficiencies, yield improvements, and process capability opportunities
• Support new product launches and technology transfers
• Optimize existing commercial manufacturing processes
• Lead technical projects from investigation through implementation
• Partner with Operations, Engineering, Quality, Procurement, and Operational Excellence
• Support equipment/process qualification and continued process verification
• Contribute to Lean, Six Sigma, and continuous improvement initiatives

MININMUM QUALIFICATIONS

• 3–5+ years of Medical Device and/or Pharmaceutical manufacturing experience
• Background in Engineering, Science, Technology, or a closely related technical discipline
• Demonstrated process and/or equipment validation experience
• Strong technical writing capabilities
• Knowledge of U.S. FDA and/or EU MDR medical device regulations
• Experience working within a GMP-regulated manufacturing environment
• Strong technical troubleshooting, analytical, and problem-solving capabilities

A Mechanical Engineering or Process Engineering background is particularly relevant, although candidates from other technical disciplines with comparable manufacturing experience are encouraged to apply.

THE ENVIRONMENT

This is an onsite, individual-contributor position for someone who enjoys having ownership.

You’ll have support while learning the site's quality systems, processes, and SOPs, but ultimately we're looking for someone who is self-driven and capable of independently moving technical projects forward.

The environment is collaborative and cross-functional, so success requires someone who can combine technical expertise with the ability to influence, communicate, and work effectively across teams.

COMPENSATION & BENEFITS

• Medical: 100% company-paid medical premiums for employees and dependents
• 401(k): 100% company match on the first 4% of employee contributions
• Additional Benefits: Tuition reimbursement and additional financial wellness resources

If your background sits at the intersection of manufacturing engineering, process improvement, validation, technical writing, and regulated medical device/pharmaceutical manufacturing, this is an opportunity to have meaningful ownership over how products and processes perform.