Manufacturing Operator

United Pharma Technologies Inc; Town of Western (NY); On-site; USD 50,000 - 70,000; Part time

Job summary

A pharmaceutical manufacturing company is seeking an experienced GMP Cleanroom Operator to support operations in a regulated cleanroom environment. The ideal candidate must have 3–5 years of experience in GMP manufacturing and a solid understanding of gowning techniques, production operations, and GMP documentation. Responsibilities include following gowning procedures, supporting clinical batch manufacturing, and maintaining compliance with strict protocols. This is a contract position suited for mid-senior level professionals.

Qualifications

• 3–5 years of experience in a GMP manufacturing environment.
• Strong background in production operations within cleanroom settings.
• Proven knowledge of gowning techniques and cleanroom behavior.

Responsibilities

• Perform production operations within a GMP-regulated cleanroom environment.
• Support Process Qualification (PQ) and GMP clinical batch manufacturing activities.
• Follow and maintain strict cleanroom gowning procedures and aseptic techniques.

Skills

GMP manufacturing experience

Production operations

Gowning techniques

Attention to detail

Job description

We are seeking an experienced GMP Cleanroom Operator to support pharmaceutical manufacturing operations in a regulated cleanroom environment. The ideal candidate will have a strong production background within GMP facilities and hands‑on experience supporting PQ activities and GMP clinical batch manufacturing. This role requires strict adherence to gowning protocols, procedures, and GMP documentation practices.

Key Responsibilities

• Perform production operations within a GMP-regulated cleanroom environment
• Support Process Qualification (PQ) and GMP clinical batch manufacturing activities
• Follow and maintain strict cleanroom gowning procedures and aseptic techniques
• Accurately complete, review, and maintain GMP documentation and batch records
• Review, understand, and sign IP (In-Process) assignments as required
• Comply with all site SOPs, safety requirements, and regulatory guidelines
• Maintain a high level of attention to detail to ensure product quality and compliance

Required Skills & Qualifications

• 3–5 years of experience working in a GMP manufacturing environment
• Strong background in production operations within cleanroom settings
• Proven knowledge of gowning techniques and cleanroom behavior
• Experience supporting PQ and GMP clinical batches
• Solid understanding of GMP documentation practices
• Ability to follow procedures precisely and work in a highly regulated environment

Preferred Qualifications

• Prior experience in pharmaceutical or biotech manufacturing
• Familiarity with clinical‑stage manufacturing operations

Seniority level

Mid‑Senior level

Employment type

Contract

Job function

Pharmaceutical Manufacturing

Other Information

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