Engineer Senior

New Albany, OH, US • Posted 18 hours ago • Updated 5 hours ago
Full Time
On-site
Fitment

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Job Details

Skills

  • Swing
  • Technical Writing
  • Veeva
  • Process Engineering
  • Process Optimization
  • Manufacturing Support
  • Network
  • IT Management
  • Manufacturing
  • Business Process
  • Productivity
  • Document Management
  • Corrective And Preventive Action
  • Change Control
  • GMP
  • Assembly
  • Project Management
  • Teamwork
  • Collaboration
  • Communication
  • Management
  • Supplier Relationship Management
  • Adaptability
  • Operational Excellence
  • Continuous Improvement

Summary

Swing shift - candidates need to have flexibility for different shifts. Dayshift / Nightshift / Weekend

10% travel required - Must be able to travel internationally for work (Europe/Canada)
18 month contract to start

Ideal Candidate: B.S. and 4 years of GMP experience, Packaging equipment experience,
technical writing & Document management system experience - KNEAT or Veeva highly preferred

The Senior Process Development Engineer - Packaging Equipment supports commercial GMP Final Drug Product (FDP) operations in New Albany, Ohio .
This is a technical leadership role requiring application of advanced engineering principles in equipment, devices, process optimization, and manufacturing support. The position requires on-site support and be able to work flexible schedule based on operation demands and both on-site work and ~10% travel

Key Functions & Outputs

Project Management:
- Support technical transfer of product portfolio into the Ohio site.
- Drive continuous improvement in device assembly and packaging line capacity/performance.
- Communicate across the network to deliver technical milestones.

Technical Leadership:
- Act as site expert in automated/semi-automated device assembly.
- Lead commissioning, qualification, and validation (CQV) of GMP equipment.
- Own and maintain the site master validation plan.

Operational Excellence:
- Analyze, design, and implement manufacturing/business process improvements.
- Drive productivity, throughput, and efficiency gains.

Quality and Document Management Systems:
- Able to author and manage various documents/protocols/reports
- Deviation/CAPA/EV Owner
- Change Control Owner

Relationships:
- Build networks with commercial and clinical operations.
- Provide support for equipment standardization, troubleshooting, and performance trending

Qualifications
- Basic (Education & Experience)
- Doctorate (no experience required)
- OR Master's + 2 years GMP experience
- OR Bachelor's + 4 years GMP experience
- OR Associate's + 8 years GMP experience
- OR High School/GED + 10 years GMP experience

Preferred
Combination product assembly equipment expertise
Cross-functional project leadership experience
Strong teamwork and communication skills
Direct experience in devices, combination products, and packaging operations
Supplier management experience (FDP equipment vendors)
Adaptability in regulated, fast-paced environments
Operational excellence / continuous improvement mindset
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.
  • Dice Id: 91160181
  • Position Id: d01cf46e44a6300808928b42effafef9
  • Posted 18 hours ago
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