
New York Technology Partners
Albany, New York • Today
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Contract, Third Party
Depends on Experience
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New York Technology Partners
Albany, New York • Today
Easy Apply
Contract, Third Party
Depends on Experience

Title: CIP/SIP and Process Qualification Engineer
Work Location Albany, NY - 5 Days Onsite
Job Type: 6+ Months Contract
KEY: *We need an Autoclave SME* (6+ years of in-depth Autoclaves validation/test exp)
Job Description
We are seeking a detail-oriented and experienced CIP/SIP and Process Validation Engineer to join our team in NY. The ideal candidate will have a strong background in Clean-In-Place (CIP), Steam-In-Place (SIP)/autoclave processes, hold times, and process validation within a regulated manufacturing environment.
Required Skills and Qualifications
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Albany, New York
•
Today
Arthur Lawrence is looking for a CIP/SIP and Process Qualification Engineer one our clients in Albany, NY. Please find the job description below and send us your updated resume if interested: Must-Have Skills:8+ years of relevant experience with SIP/autoclave processes, CIP systems, and process qualification. Strong knowledge of hold times, process validation, cleaning validation, and related regulatory requirements. Excellent documentation and communication skills with the ability to work ind
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Third Party, Contract
Depends on Experience
Rensselaer, New York
•
Today
Build our future together: Regeneron is seeking a Process Controls & Validation Engineer to join our Process Sciences Drug Product Engineering department. Process Sciences is a technical services department that deals with a range of scientific, technical, engineering and mathematical needs from the laboratory to the manufacturing floor. This non-lab based role focusing on fill finish operations provides technical support to manufacturing, quality and CMC Regulatory for manufacturing processes
Full-time
USD 62,355.00 - 110,000.00 per year
Albany, New York
•
Today
Job Description: The Senior Computer System Validation (CSV) Engineer is responsible for leading validation activities for computerized systems used in regulated environments such as pharmaceutical, biotechnology, or medical device manufacturing. This role ensures that systems including LIMS, ERP, MES, and laboratory applications are validated in compliance with FDA, EU, and global regulatory requirements. The Senior CSV Engineer will act as a subject matter expert (SME), providing guidance on v
Full-time
Rensselaer, New York
•
Today
Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We're seeking a Process Controls & Validation Engineer with a strong background in cGMP validation, who can develop sound process control strategy, bring structure to ambiguous technical problems, and confidently lead and influence discussions across Manufacturing, Quality and Regulatory teams. Process Sciences is a technical services department that deals
Full-time
USD 67,400.00 - 128,700.00 per year