EQVAL Group, Inc logo
EQVAL Group, Inc
Posted 6 days agoVerified live 2d ago

Process Development Engineer

Brief overview

Remote
UndergradOr in progress
3+ yrsMinimum
Process ValidationEquipment Qualification (IQ/OQ/PQ)Regulated Manufacturing PharmaceuticalRegulated Manufacturing BiotechRegulated ManufacturingRegulated Manufacturing Medical DevicesLaser WeldingHeat BondingInjection MoldingVision SystemsAutomation and ControlsTooling and FixturesTest Method DevelopmentDesign of Experiments (DOE)Failure Mode and Effects Analysis (FMEA)Corrective and Preventive Action (CAPA)Root-Cause Investigation

About the company

EQVAL Group, Inc logo
EQVAL Group, Inceqvalpr.com

EQVAL Group, Inc.

Job description

Summary

EQVAL Group, Inc. provides services to the manufacturing industry, including medical devices, pharmaceuticals, and biotechnology. The Process Development Engineer supports the development, validation, and implementation of new manufacturing processes through documentation generation, process optimization, equipment qualification, and cross-functional collaboration.

Responsibilities

  • Perform process validation and equipment qualification activities / reports (IQ, OQ, PQ) and develop Master Validation Plans
  • Generate equipment documentation (evaluations, PM/calibration procedures) and manufacturing instructions
  • Design and develop in‑process and receiving inspection systems for new components and processes
  • Characterize, optimize, and improve manufacturing processes through DOE, PFMEA, and risk analysis
  • Work with technologies such as laser welding, heat bonding, injection molding, vision systems, and automation (PLC/servo/pneumatics/sensors)

Skills

  • Bachelor Degree in Engineering
  • Previous experience in regulated industry (Pharma, Biotech, or Medical Devices)
  • Experience with automated manufacturing system and equipment (laser welding, heat bonding, injection molding, vision systems)
  • Experience with automation/controls, tooling, fixtures, test method development
  • Proficiency in DOE, FMEA, CAPA, and root‑cause investigation
  • Good technical writing skills
  • Fully bilingual (English and Spanish)
  • Electrical and Mechanical backgrounds preferred

Qualifications

Must Haves

  • Bachelor Degree in Engineering
  • Previous experience in regulated industry (Pharma, Biotech, or Medical Devices)
  • Experience with automated manufacturing system and equipment (laser welding, heat bonding, injection molding, vision systems)
  • Experience with automation/controls, tooling, fixtures, test method development
  • Proficiency in DOE, FMEA, CAPA, and root‑cause investigation
  • Good technical writing skills
  • Fully bilingual (English and Spanish)

Nice to Haves

  • Electrical and Mechanical backgrounds preferred

Benefits

  • Health insurance (Medical, Dental, Vision, Pharmacy)
  • Life Insurance
  • Paid time off (PTO)
  • Holidays
  • Professional Growth (Courses and Certifications by EQVAL Academy)
  • Referral program
  • Productivity incentive

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