Katalyst CRO logo
Katalyst CRO
Posted 21 days agoVerified live 17h ago

Project Engineer

Brief overview

Remote
UndergradOr in progress
4+ yrsMinimum
32 H-1B approvalsDept. of Labor
9 green cardsCertified filings
Pharmaceutical GMPEquipment DesignPFD/P&ID DevelopmentManufacturing Equipment CommissioningEquipment QualificationPLC Control SystemsProcurement and ContractingAutomation EngineeringControls EngineeringDrug Product ManufacturingOral Solid Dosage ManufacturingVerification and Qualification DocumentationFactory Acceptance Tests (FAT)Site Acceptance Tests (SAT)Software Acceptance TestsCQV / ValidationAutomation and HMI

About the company

Katalyst CRO logo
Katalyst CROkatalysthls.com

Katalyst CRO | Advancing Healthcare & Life Sciences with Expert Research & Regulatory Solutions Katalyst Healthcare & Life Sciences (Katalyst CRO) is a Global Contract Research and Knowledge Process Outsourcing Organization (CRO) dedicated to driving innovation in research, regulatory compliance, and quality excellence for pharmaceutical, biotechnology, and medical device companies worldwide.

Visa sponsorship history

4 years sponsoring, last filed FY2026

Data powered by U.S. Department of Labor. This does not guarantee sponsorship for this specific role.
32H-1B approved
89%approval rate
3new H-1B hires
9PERM certified
$240,000median wage / yr
H-1B Petition ApprovalsVisas USCIS actually granted: the strongest sign the company sponsors.
202319
20249
20254
LCA Certified ApplicationsAn early filing step, not a visa approval: it signals intent, not confirmed sponsorship.
20236
20242
20259
20262
Green Card (PERM) FilingsCertified green card filings: a long-term commitment to international hires.
20235
20241
20253
Top sponsored roles
VALIDATION ENGINEERQUALITY ENGINEERCLINICAL DATA ANALYSTPRODUCT DEVELOPMENT ENGINEERCLINICAL DATA MANAGER
Sponsored employees from
India

Job description

Summary

Katalyst CRO is seeking a Project Engineer who will manage medium size projects from concept to closure with minimal supervision. The role involves financial management, contractor oversight, and collaboration with various teams to ensure project success in a manufacturing plant environment.

Responsibilities

  • Responsible for supporting capital projects in the manufacturing plant, including front end planning activities
  • Coordinate multiple parties to complete project scopes on schedule, stay within budget and meet the expected quality
  • Assist with design of new equipment systems from preliminary design, specifications, budgeting, scheduling, and construction management
  • Develop project schedules including setting targets for milestone activities and adhering to deadlines
  • Track progress to ensure the project scope, cost, and schedule are being met Manage the life-cycle documentation of the equipment including generation and approval of user requirements, equipment and instrument specifications, equipment test plans, and system operating procedures
  • Develop documents for FAT, SAT, and qualification activities for equipment
  • Participate in FAT, SAT, startup, commissioning and qualification of equipment
  • Write scope of work documents, award contracts, obtain estimates, select suppliers, and purchase equipment and services
  • Review drawings, supervise contractors, and participate in final project acceptance upon completion of construction
  • Making effective decisions when presented with multiple options for how to progress with the project
  • Communicating with management to keep the project aligned with their goals
  • Performing quality control on the project throughout development to maintain the standards expected

Skills

  • Bachelor's Degree in Engineering, Science, or closely related discipline, or equivalent technical experience plus demonstrated competence
  • Technical background in Pharmaceutical or similar GMP-regulated industry
  • Expertise in equipment design, design specifications, and PFD/P&ID development
  • Experience with manufacturing equipment commissioning and qualification
  • Familiarity with PLC control systems
  • Interacts well with diverse groups within engineering and maintains strong working relationships with internal and external collaborators
  • Listens to and understands others' points of view and articulates tactfully and respectfully one's own perspective orally, in writing, and in presentations
  • Works well with other engineers in a collaborative, fast-paced goal-driven environment
  • Possesses interpersonal skills to negotiate and reconcile differences
  • Understanding and management of procurement & contracting processes
  • Experience with automation and controls engineering
  • Experience with drug product and oral solid dosage manufacturing and equipment
  • 4+ years experience
  • Bachelor's degree (mandatory)
  • OSD / Pharma equipment experience
  • Capital project exposure
  • CQV / Validation experience
  • Automation & HMI exposure
  • Strong communication skills
  • Chemical or Mechanical Engineering degree strongly preferred
  • Experience with automation and controls engineering preferred
  • Experience with drug product and oral solid dosage manufacturing and equipment preferred

Qualifications

Must Haves

  • Bachelor's Degree in Engineering, Science, or closely related discipline, or equivalent technical experience plus demonstrated competence
  • Technical background in Pharmaceutical or similar GMP-regulated industry
  • Expertise in equipment design, design specifications, and PFD/P&ID development
  • Experience with manufacturing equipment commissioning and qualification
  • Familiarity with PLC control systems
  • Interacts well with diverse groups within engineering and maintains strong working relationships with internal and external collaborators
  • Listens to and understands others' points of view and articulates tactfully and respectfully one's own perspective orally, in writing, and in presentations
  • Works well with other engineers in a collaborative, fast-paced goal-driven environment
  • Possesses interpersonal skills to negotiate and reconcile differences
  • Understanding and management of procurement & contracting processes
  • Experience with automation and controls engineering
  • Experience with drug product and oral solid dosage manufacturing and equipment
  • 4+ years experience
  • Bachelor's degree (mandatory)
  • OSD / Pharma equipment experience
  • Capital project exposure
  • CQV / Validation experience
  • Automation & HMI exposure
  • Strong communication skills

Nice to Haves

  • Chemical or Mechanical Engineering degree strongly preferred
  • Experience with automation and controls engineering preferred
  • Experience with drug product and oral solid dosage manufacturing and equipment preferred

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