Commissioning Consultant

Vantage Consulting; New York (NY); On-site; USD 80,000 - 100,000; Full time

Job summary

An established industry player is seeking a Commissioning Engineer to support vital commissioning activities in a fill/finish production line. This role involves executing protocols, managing vendor coordination, and ensuring compliance with GMP standards. The ideal candidate will have 2-3 years of relevant experience, strong documentation skills, and the ability to work collaboratively across teams. Join a dynamic environment where your contributions will enhance operational readiness and efficiency in pharmaceutical manufacturing.

Benefits

401(k)

Vision Insurance

Medical Insurance

Qualifications

• 2–3 years of commissioning experience in pharmaceutical manufacturing.
• Strong documentation and communication abilities required.

Responsibilities

• Support commissioning efforts and manage protocol execution.
• Maintain GMP-compliant documentation and collaborate with vendors.

Skills

Commissioning Experience

Documentation Skills

Communication Skills

GMP Guidelines

Collaboration Skills

Tools

Microsoft Project

Job description

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This range is provided by Vantage Consulting. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$80.00/hr - $90.00/hr

Overview:

A leading pharmaceutical manufacturer is seeking a Commissioning Engineer to support commissioning activities on a fill/finish production line. The role will focus on protocol execution, vendor coordination, and documentation in compliance with GMP standards.

Key Responsibilities:

• Support commissioning efforts post-FAT phase, including SAT protocol execution
• Manage and execute protocols for alarms, functional testing, and calibration
• Maintain detailed, GMP-compliant documentation throughout all phases
• Interface directly with vendors and internal teams to drive completion of punch lists
• Collaborate with validation and facilities compliance teams to ensure operational readiness

Required Qualifications:

• 2–3 years of commissioning experience (FAT/SAT, IQ/OQ/PQ support)
• Strong documentation skills and communication abilities
• Experience working under GMP guidelines and with SOPs
• Ability to collaborate across cross-functional engineering and compliance teams
• Must be eligible to work on a W2 basis

Preferred Qualifications:

• Experience with fill/finish production lines
• Background in pharmaceutical manufacturing environments
• Familiarity with Microsoft Project

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Industries

  Pharmaceutical Manufacturing

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Inferred from the description for this job

401(k)

Vision insurance

Medical insurance

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