cqv

**Job Description**- We are seeking a CQV Specialist to lead commissioning, qualification, and validation activities for facility, equipment, and computerized systems supporting GMP cell therapy manufacturing. This individual will own qualification strategy and execution, ensuring compliant, risk-based validation aligned with USP , GAMP 5, and industry best...

Full time roleCQV EngineerColumbus OH, Onsite CQV Engineer Responsibilities:Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and processes as part of a team as directed by the project leaderRunning test scripts and documenting resultsAdherence ...

Job Description: We are looking for CQV Engineers / System Owners to take ownership of specific process and utility systems within either the Bulk (Drug Substance) or Fill Finish (Drug Product) areas on a large-scale greenfield project. This role focuses on system ownership across the full CQV lifecycle, from design review through to qualification...

Summary : Seeking a CQV Validation Engineer experience in pharmaceutical, biotech, or life sciences. The ideal candidate will have hands-on experience with Commissioning, Qualification & Validation (CQV) for standalone manufacturing equipment in a GMP-regulated environment. Roles & Responsibilities : Perform CQV activities for standalone equipment....

Job description We are seeking a Senior CQV Specialist to lead commissioning, qualification, and validation activities for facility, equipment, and computerized systems supporting GMP cell therapy manufacturing. This individual will own qualification strategy and execution, ensuring compliant, risk-based validation aligned with USP , GAMP 5, and industry...

Job description: We are seeking a CQV Specialist to lead commissioning, qualification, and validation activities for facility, equipment, and computerized systems supporting GMP cell therapy manufacturing. This individual will own qualification strategy and execution, ensuring compliant, risk-based validation aligned with USP , GAMP 5, and...

Job Summary: The client is seeking a Commissioning and Design Engineer to join their engineering and automation team for a pharmaceutical facility in Rensselaer, New York. This role involves supporting the full commissioning lifecycle of stainless-steel pressure vessels in a new facility, including design, FAT/SAT, IQ/OQ/PQ, and...

Mace combines global delivery consultancy experience to unlock potential in every person or project and redefine the boundaries of ambition. Our values shape the way we consult and define the people we want to join us on our journey.You’ll be responsible for:Lead safe, compliant and sustainable delivery, applying strong knowledge of local Health and Safety...

Job Description: We are looking for CQV Engineers / System Owners to take ownership of specific process and utility systems within either the Bulk (Drug Substance) or Fill Finish (Drug Product) areas on a large-scale greenfield project. This role focuses on system ownership across the full CQV lifecycle, from design review through to qualification...

Job Description: We are looking for CQV Engineers / System Owners to take ownership of specific process and utility systems within either the Bulk (Drug Substance) or Fill Finish (Drug Product) areas on a large-scale greenfield project. This role focuses on system ownership across the full CQV lifecycle, from design review through to qualification...

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 line The role is as follows Work remote (initially) on the Clients Global C&Q team Be the C&Q SME on the Client's project team to apply the...

 CQV EngineerBend, ORThe actual location of this job is in Bend, Oregon (USA). Relocation assistance is available for eligible candidates and their families, if needed.Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is...

Job description: We are seeking a CQV Specialist to lead commissioning, qualification, and validation activities for facility, equipment, and computerized systems supporting GMP cell therapy manufacturing. This individual will own qualification strategy and execution, ensuring compliant, risk-based validation aligned with USP , GAMP 5, and...

Responsibilities: Manage the validation and documentation related to complex computer systems, multiple pieces of equipment/large upgrades/extensive product updatesPerform functions of validation engineer – draft Validation Plans, Requirements, Test Cases, Summary ReportsManage the systems and processes for change control and coordinate evaluation of...

Job Summary: We are seeking a CQV Lead (OSD Manufacturing) with strong engineering fundamentals and hands-on experience in commissioning, qualification, and validation within a GMP-regulated Oral Solid Dose (OSD) environment. This role involves leading end-to-end CQV activities for manufacturing equipment, packaging systems, utilities,...

Summary: Seeking a CQV Validation Engineer with 5+ years of experience in pharmaceutical, biotech, or life sciences. The ideal candidate will have hands-on experience with Commissioning, Qualification & Validation (CQV) for standalone manufacturing equipment in a GMP-regulated environment. Roles & Responsibilities: Perform CQV activities for...

Job Description: We are looking for CQV Engineers / System Owners to take ownership of specific process and utility systems within either the Bulk (Drug Substance) or Fill Finish (Drug Product) areas on a large-scale greenfield project. This role focuses on system ownership across the full CQV lifecycle, from design review through to qualification...

Job description: We are seeking a Senior CQV Specialist to lead commissioning, qualification, and validation activities for facility, equipment, and computerized systems supporting GMP cell therapy manufacturing. This individual will own qualification strategy and execution, ensuring compliant, risk-based validation aligned with USP , GAMP...

Designing validation plans.Conducting and documenting impact and risk assessments with a full understanding of equipment/system/ software operation and ability to assess direct, indirect, and no impact systems and functions within complex processesMaintaining (and ensuring the team maintains) clear, detailed records of qualification and validation, and...

Job description: We are seeking a CQV Specialist to lead commissioning, qualification, and validation activities for facility, equipment, and computerized systems supporting GMP cell therapy manufacturing. This individual will own qualification strategy and execution, ensuring compliant, risk-based validation aligned with USP , GAMP 5, and industry best...