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📑 Lead CQV CIP Engineer - Pharmaceuticals - Raleigh, NC - 12-Month Contract Our client, a global Pharmaceutical manufacturing organization are looking for a talented Lead CQV CIP Engineer to join their expanding team. With continued organizational growth and considerable investment across their portfolio and capital programs this ...

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📑 Piper Life Sciences is actively seeking a CQV Clean Utilities Engineer to join a pharmaceutical manufacturing facility that is brand new and going to be the largest end-to-end cell manufacturing facility in Northern America.. The CQV Clean Utilities Engineer will act as the client's agent to review and approve submitt ...

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📑 Responsibilities: Executes the commissioning, qualification, requalification, validation and any associated maintenance activities within the plant. Manages multiple and complex CQV projects, provides status reports and coordinates with other departments or outside contractors/vendors to complete t ...

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📑 Job Title: Lead CQV Engineer/Analyst Location: Columbus, OHJob Type : Full Time JOB DESCRIPTIONLead CQV Engineer/AnalystThis role is 100% onsite at the Easton, OH location. The role requires strong validation skills and ex ...

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📑 Senior CQV EngineerSyracuse, NY, United StatesContractSenior CQV Engineer Responsibilities:• Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and processes as part of team as directed by the project leader• Running te ...

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📑 PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients success, and you can be a part of our teams achievements. Employing a global team of ...

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📑 Responsibilities: Responsible for providing quality oversight for the qualification and validation activities for equipment, utilities, and facilities. This role will be responsible for drafting, reviewing and approving qualification protocols/reports and any associated documentation in support o ...

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📑 Responsibilities: Responsible for providing quality oversight for the qualification and validation activities for equipment, utilities, and facilities. This role will be responsible for drafting, reviewing and approving qualification protocols/reports and any associated documentation in support of ...

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📑 Responsibilities: Support protocol/report generation and on the floor test execution, for various opex and capex projects, and anything else related to cleaning and facilities, equipment, and utility (FEU) validation and requalification activities. Complete temperature mapping. ...

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📑 Responsibiltiies: Develop comprehensive protocols for the qualification/requalification of new and existing QM micro and QC analytical equipment. Develop comprehensive protocols for the qualification of required clean utilities to service new QC Micro and QC analytical laboratory. ...

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📑 Responsibilities: Validation Planning and Strategy: Develop and implement validation plans and strategies in alignment with current Good Manufacturing Practices (cGMP), FDA, EMA, and other regulatory guidelines. Commissioning, Qualification, and Validation (CQV): Lead and execute CQV activities for ...

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📑 Role: CQV/CSVlocation: Edison, NJRelocation: Need to be open for relocation anywhere in the USATraining into Technology: Training will be provided in CQV/ CSV/ Pharma Equipment Validation (In-House Training)Experience: 3 + years relat ...

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📑 PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients success, and you can be a part of our teams achievements. Employing a global team of ...

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📑 PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients success, and you can be a part of our teams achievements. Employing a global team of ...

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📑 PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients success, and you can be a part of our teams achievements. Employing a global team of ...

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📑 Title: Project Engineer IIILocation: Houston, TX - 77047Duration: 6 MonthsDescription:The Project Engineer role supports ongoing Client operations by providing technical leadership as it relates to manufacturing and process systems. The role acts as a technical resource ...

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📑 PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients success, and you can be a part of our teams achievements. Employing a global team of ...

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📑 Job Title: Project EngineerLocation: 14905 Kirby Drive, Houston TX 77047Duration: 06+ MonthsDescription:The Project Engineer role supports ongoing operations by providing technical leadership as it relates to manufacturing and process systems.The rol ...

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📑 Job Title: Project EngineerLocation : Houston, TX 77047Duration: 6 monthsPosition Type: Hourly contract Position (W2 only)Description: The Project Engineer role supports ongoing Client operations by providing technical leadership as it relates to ma ...

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📑 PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients success, and you can be a part of our teams achievements. Employing a global team of ...

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📑 PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients success, and you can be a part of our teams achievements. Employing a global team of ...

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📑 Responsibilities: Develop commissioning and qualification protocols for HVAC, purified water systems, clean utilities, and other critical utilities according to regulatory requirements (GMP, FDA, etc.). Execute commissioning and qualification activities for utilities systems, ensuring adherence to ...

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📑 PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients success, and you can be a part of our teams achievements. Employing a global team of ...

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📑 new facility consumerisation and new syringe filling line Contractor Tasks and Responsibilities.The project is in Preliminary Design phase and consists of a new facility consumerization and new syringe filling lineThe role is as followsWork remote (initially) on the Cl ...

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📑 Responsibilities: Draft and implement Quality System documentation designed to establish good validation practices within the organization. Author URS, IQ, OQ and PQ protocols and execute them in compliance with GDP guidelines and internal quality standards. Design validation a ...

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📑 Responsibilities: Develop commissioning and qualification protocols for HVAC, purified water systems, clean utilities, and other critical utilities according to regulatory requirements (GMP, FDA, etc.). Execute commissioning and qualification activities for utilities systems, ensuring adherence to ...

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📑 Responsibilities: Support qualification activities for facility and equipment Provide technical and validation support for capital projects on site working with facilities, and manufacturing, Quality Control and Quality Assurance (QA) teams. Lead validation activities and ...

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📑 PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients success, and you can be a part of our teams achievements. Employing a global team of ...

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📑 Responsibilities: Seeking proposals to support the relocation of QC microbiology and QC analytical equipment from current labs to a new facility. This includes approximately 50 pieces of GMP equipment, primarily benchtop lab equipment like QC-M and QC-analytical instruments, which will require qua ...

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📑 PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients success, and you can be a part of our teams achievements. Employing a global team of ...

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📑 An exciting clinical-stage biotech company, located in the Los Angeles area, is seeking a talented professional to join a their team as a Senior Quality Engineer. Key Responsibilities:Ensure continuous validation of Equipment, Facilities, Utilities, and Computer Systems.Spearhead validation initiatives to a ...

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📑 Industry: BiotechnologyPosition: Principal Commissioning/Validation Engineer III Location: Framingham, MA - 01701Duration: 06 months contract (+Possibility of extension)Requirements:BSc/BEng plus previous experience ...

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📑 Responsibilities: Bachelor's degree in mechanical, Chemical, or Electrical Engineering or equivalent years of experience in lieu of degree At least 8 years of CQV experience in the Life Sciences industry Understanding of Good Manufacturing Practices (GMPs) Stro ...

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📑 Day-to-DayInsight Global is seeking a junior Automation Engineer to join one of our top pharmaceutical clients in Plainville, MA. This individual will be responsible for supporting the facility with a scope encompassing automation systems for GMP Manufacturing, Quality Control, Process Development, and their Warehouse Ope ...

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📑 Position: Principal Commissioning/Validation Engineer III, Req#: SNFIJP00008706Location: Framingham, MA (100% onsite)Duration: 6 Months ContractJob Description:Education and Experience: < ...

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📑 PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients success, and you can be a part of our teams achievements. Employing a global team of ...

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📑 SummaryDPS Group is seeking a talented HVAC Lead to support our client. Successful candidates will act as the Primary HVAC interface during the project and deliver a high-end facility with respect to the HVAC scope, in line with industry best practices, within budget and schedule, without compromising safety. < ...

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📑 Responsibilities: Develop and approve cGMP documents including, but not limited to: Equipment and instrument Qualification, Commissioning, Master Validation Plans, SOP's, Comparability reports, Aseptic Process simulation protocols and reports; process validation (PPQ), and cleaning/sterilization validation. ...

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📑 Verista's 600 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing healthcare c ...

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📑 Verista's 600 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing healthcare c ...

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📑 Role: Validation LeadLocation: Los Angeles, CA, 90039Duration: Long Term ContractJob Description:Develop validation documentation such as validation plans, functional design specifications, test protocols, and standard operation proced ...

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📑 Verista’s 600 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verist ...

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📑 Verista’s 600 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verist ...

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📑 Verista’s 600 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verist ...

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📑 Responsibilities: Extensive expertise in the execution of manufacturing equipment, including assembly line, room qualification, utilities, CTEs, using a risk-based approach for quality documentation generation. Self-motivated and proactive Possesses the ability to work independ ...

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📑 Responsibilities: Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and processes as part of team as directed by the project leader. Running test scripts and documenting results. Adhere ...

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📑 Responsibilities: Extensive expertise in the execution of manufacturing equipment, including assembly line, room qualification, utilities, CTEs, using a risk-based approach for quality documentation generation. Self-motivated and proactive. Possesses the ability to work indepe ...

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📑 Responsibilities: Engineer will be responsible for the qualification of an ESCO isolator system. Responsible for the creation and execution of validation protocols. Responsible for reviewing existing documentation and determining necessary additional testing per Annex 1 requirement ...

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📑 <p style="margin-bottom:11px">Lead CQV Engineer Responsibilities:12-14 years experience<br /> Title: Syracuse,NY onsite</p> <p style="margin-bottom:11px">All candidates will need expertise in Production Equipment, Facilities (Clean Room Qualification with EMPQ), and Utilities (WFI, HVAC ...

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📑 WHO?If you’re looking to be part of something special, making a difference to society through improved patient therapies and care, this could be the opportunity for you!INCOG BioPharma Services is seeking a Senior MSAT Engineer to join them on their journey in delivering their world class CDMO ...

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