United Pharma Technologies Inc
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 Referrals increase your chances of interviewing at United Pharma Technologies Inc by 2x
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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 Referrals increase your chances of interviewing at United Pharma Technologies Inc by 2x
Get notified about new Manufacturing Operator jobs in
Western, NY .
#J-18808-Ljbffr