Cleaning and Process Validation

Job Title:- Cleaning and Process ValidationLocation:- Hopewell, NJJob Description:-Support SAT, system walkdown, design review for CIP skids, Bioreactors, Autoclave, Parts washer, Filling Line, Isolators.Author protocol for IQ, OQ and PQ.CIP and COP Cycle development.Cleaning and Process Validation.Excellent communication and teamwork skills.Flexible to...

Cleaning and Process Validation Job DescriptionAt Intellectt Inc, we are seeking a highly skilled Cleaning and Process Validation professional to join our team.Key Responsibilities:Support SAT, system walkdown, design review for CIP skids, Bioreactors, Autoclave, Parts washer, Filling Line, Isolators.Author protocol for IQ, OQ and PQ.CIP and COP Cycle...

We are seeking an experienced CIP/SIP Cleaning Validation Engineer to support our client, at their facility in Hopewell, NJ. The ideal candidate will have expertise in Cleaning-In-Place (CIP) and Steam-In-Place (SIP) systems, PID controller tuning, hydraulic balance, and flow calculations. This role requires excellent communication and teamwork skills,...

Job SummaryWe are seeking a highly skilled Validation Engineer II to join our team at BeiGene. As a key member of our Validation function, you will be responsible for ensuring the successful management of related activities and large projects, while supporting Validation objectives and adhering to regulatory compliance and achieving commercial success.Key...

Automation Validation Engineer Location: Hopewell, NJWhy You Should Apply:Integral role in the startup of a new biopharmaceutical manufacturing facility.Opportunity to work with a dynamic engineering team in a leading biotech company.Engage in diverse tasks from P&ID review to system integration and validation.Hands-on experience with cutting-edge...

We are hiring an experienced Automation Validation Engineer to contribute to the successful launch of our new manufacturing facility. This role offers the opportunity to work on innovative biopharmaceutical processes, making a meaningful impact in a fast-growing industry.Responsibilities:Support IO Check, system integration, and validation for startup...

Job Title: Industrial Cleaning SupervisorAt Mpwservices, we are seeking a highly skilled and experienced Industrial Cleaning Supervisor to join our team. As an Industrial Cleaning Supervisor, you will be responsible for overseeing the execution of industrial cleaning operations at various sites, ensuring the highest level of quality and safety standards are...

Role: CQV EngineerLocation: Boston, MAType: Long Term Contract Key Responsibilities:Perform qualification and process engineering tasks.Conduct validation activities for fill finish lines, isolators, and autoclaves.Develop and execute validation protocols and reports.Ensure compliance with GMP and regulatory standards.Collaborate with cross-functional teams...

Job Title: Process EngineerWestRock is seeking a skilled Process Engineer to join our team. As a Process Engineer, you will be responsible for managing technical projects aimed at product and process problem solving and/or improvements, cost reduction, and profitability improvement.Key Responsibilities:Provide technical assistance to operating departments to...

Job Title: Process EngineerWestRock is seeking a skilled Process Engineer to join our team. As a Process Engineer, you will be responsible for managing technical projects aimed at product and process problem solving and/or improvements, cost reduction, and profitability improvement.Key Responsibilities:Provide technical assistance to the operating...

Job SummaryWe are seeking a highly skilled and experienced Sterile Processing Supervisor to join our team at STERIS. As a key member of our operations team, you will be responsible for ensuring the efficient and effective reprocessing of surgical instruments and trays in compliance with regulatory standards and facility goals.Key ResponsibilitiesOversee...

About GenScript/ProBioGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group with a presence across North America, Europe, the Greater China, and Asia Pacific. Our businesses encompass four major categories based on our leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology...

Job Title: Bioprocess Specialist - Upstream ProcessingWe are seeking a highly skilled Bioprocess Specialist - Upstream Processing to join our team at GenScript/ProBio. As a key member of our Upstream Processing group, you will be responsible for executing upstream operations, including preparation of stock solutions, buffers, and media, filtration of stock...

Key Responsibilities:Following cGMP procedures to support manufacturing execution and automated recipe processes.Conducting Clean-In-Place (CIP) and Steam-In-Place (SIP) procedures.Preparing and transferring media, including filtration.Sampling, monitoring, and transferring cell cultures.Managing harvest operations.Troubleshooting equipment and process...

Key Responsibilities:Following cGMP procedures to support manufacturing execution and automated recipe processes.Conducting Clean-In-Place (CIP) and Steam-In-Place (SIP) procedures.Preparing and transferring media, including filtration.Sampling, monitoring, and transferring cell cultures.Managing harvest operations.Troubleshooting equipment and process...

Job Title: Biologic Drug Product Manufacturing Process ExpertAmpcus Incorporated is a certified global provider of a broad range of Technology and Business consulting services. We are seeking a highly motivated Biologic Drug Product Manufacturing Process Expert to join our talented team.Job Summary:The Biologic Drug Product Manufacturing Process Expert will...

Key Responsibilities:Executing manufacturing processes in accordance with cGMP guidelines to ensure product quality and compliance.Conducting thorough Clean-In-Place (CIP) and Steam-In-Place (SIP) procedures to maintain equipment integrity.Preparing and transferring media, including filtration, to support cell culture growth.Sampling, monitoring, and...

This is a contract until 01/31/2025, with the opportunity to extend longer or convert to FTE based on budget/performance. Benefits: (Medical, Dental, Vision, Life Insurance)Follow cGMP procedures to support manufacturing execution and automated recipesClean-In-Place (CIP) & Steam-In-Place (SIP)Media preparation & transfers / filtrationCell culture sampling,...

General Description:The Cell Culture Manufacturing Senior Technician position will directly enable the initial start-up phase of the Hopewell manufacturing facility and then shift focus to hands-on execution and support of cGMP manufacturing operations.Hands-On cGMP Operations: Focused on execution of cGMP manufacturing activities required to deliver the...

General Description:The Cell Culture Manufacturing Senior Technician position will directly enable the initial start-up phase of the Hopewell manufacturing facility and then shift focus to hands-on execution and support of cGMP manufacturing operations.Hands-On cGMP Operations: Focused on execution of cGMP manufacturing activities required to deliver the...