6085 - Senior CQV Engineer / Senior Validation Engineer - Holly Springs, NC

+Job summary · The Senior CQV Engineer is responsible for leading and executing Commissioning, Qualification, and Validation (CQV) activities with a strong focus on CIP systems supporting Drug Substance Manufacturing.ResponsibilitiesCQV & Validation ExecutionLead and execute comm ...

Job Title: Pharmaceutical Validation Engineer · Location: Holly Springs NC · Duration: 09 Months · Description: · Note: Fully Onsite · Standard Working Hours 8:00AM - 5:00PM · Top 3 Must Have Skill Sets: · Inspection · Shut down · Validation · Primarily responsible for ensuring a ...

Job Title: Senior Validation Engineer · Location: Holly Springs NC · Duration: 12+ Months · Note: Fully Onsite · Standard Working Hours 8:00AM - 5:00PM · Description: · Primarily responsible for ensuring adherence to computer validation standards and procedures for computer rela ...

Job summary · Aptask Global Workforce (AGW) is seeking a Process Validation Engineer for a contract. · Support the process validation team in initiation, design and delivery of projects. · ...

Job Description · Pay range: $54-64/hr · depending on exp · Primarily responsible for ensuring adherence to computer validation standards and procedures for computer related systems. Responsibilities include participation in system design, preparation of test protocols, analysis ...

ApTask Global Workforce (AGW) is seeking a Validation Engineer Senior with a technology company. This is a 9+ month contract opportunity with our client located in Holly Springs, NC. This is an onsite position. · Summary: · This role is primarily responsible for ensuring adherenc ...

Payrate: $ $55.00/hr. · Responsibilities: · Primarily responsible for ensuring adherence to computer validation standards and procedures for computer-related systems. · Responsibilities include participation in system design, preparation of test protocols, analysis of test resul ...

· Description · Verista's 500 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, organizatio ...

The Senior CQV Engineer is responsible for leading and executing Commissioning, Qualification, and Validation (CQV) activities with a strong focus on CIP systems supporting Drug Substance Manufacturing. · ...

The Senior CQV Engineer is responsible for leading and executing Commissioning, Qualification, and Validation (CQV) activities with a strong focus on CIP (Clean-In-Place) systems supporting Drug Substance Manufacturing. · ...

The Senior CQV Engineer is responsible for leading and executing Commissioning, Qualification, and Validation (CQV) activities with a strong focus on CIP systems supporting Drug Substance Manufacturing. · This role will serve as a technical subject matter expert for CIP system qu ...

The Senior CQV Engineer – Utilities CQV Lead is responsible for leading and executing Commissioning, Qualification, · and Validation (CQV) activities for critical GMP utilities systems supporting pharmaceutical and biopharmaceutical manufacturing operations.This role serves as th ...

The Senior CQV Engineer – Utilities CQV Lead is responsible for leading and executing Commissioning, Qualification, and Validation (CQV) activities for critical GMP utilities systems supporting pharmaceutical and biopharmaceutical manufacturing operations. · ...

The Senior CQV Engineer is responsible for leading and executing Commissioning, Qualification, and Validation (CQV) activities with a strong focus on CIP systems supporting Drug Substance Manufacturing. This role will serve as a technical subject matter expert for CIP system qual ...

The Senior CQV Engineer – Utilities CQV Lead is responsible for leading and executing Commissioning, · Qualification, · and Validation (CQV) activities for critical GMP utilities systems supporting pharmaceutical · and biopharmaceutical manufacturing operations. · This role serve ...

Piper Companies is seeking a Validation Engineer for a long-term contract opportunity at a leading pharmaceutical manufacturing site. · ...

The company is hiring a Validation Engineer to execute validation protocols for critical equipment and processes ensuring compliance with regulatory standards and company procedures. · ...

Piper Companies is hiring a Validation Engineer for a pharmaceutical manufacturing company located in Clayton, NC. · ...

Piper Companies is seeking a Validation Engineer to join a growing leader in the pharmaceutical/biotechnology space for an onsite contract position. · ...

Position Summary · We are seeking a highly skilled Commissioning, Qualification & Validation (CQV) Engineer to support large-scale biopharmaceutical and life sciences projects. This role is responsible for the planning and execution of commissioning, qualification, and validation ...