Validation & Engineering Group, Inc. Jobs in United States

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the position of CSV / Manufacturing Eng. Specialist. · ...

+Job summary · Hands on CQV/validation work supporting device assembly and automation projects for a combination autoinjector product.Bachelor's degree in Engineering, Life Sciences, or related field. · ...

We are seeking a talented dedicated individual committed to work under the highest ethics standards for the following position QA Lab Equipment Qualification Scientist. · Develop and execute qualification documents including CSV test scriptsChange Control OwnerReview and approve ...

We are seeking a talented Process Engineer for Dry Granulation with experience in pharmaceutical industries. · ...

Hands on CQV/validation work supporting device assembly and automation projects for a combination autoinjector product. · ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: · ...

The Commissioning and Qualification (C&Q) Specialist for Utilities and Facilities is responsible for ensuring the qualification and validation of critical utility systems and facility infrastructure in a GMP-regulated environment. · ...

We are seeking an experienced Project Manager to lead projects from construction and installation through commissioning, qualification (C&Q), and final validation of production, packaging, and utility/facility systems in a regulated manufacturing environment. · Oversee the entire ...

The Engineering Technical Lead – Biotech Facilities Design is responsible for providing technical leadership and coordination in the design of biotechnology and pharmaceutical facility projects. · ...

We are seeking a talented dedicated individual committed to working under the highest ethical standards for the following position: · ...

We are seeking an experienced Project Manager to coordinate automation and CQV projects within a Quality Assurance (QA) Laboratory. · Bachelor's degree in Engineering, Life Sciences, or a related field. · Minimum of 5 years of project management experience in a GMP - regulated la ...

We are seeking for talented, dedicated individuals who is committed to work under the highest standards of ethics to and with expertise in Packaging Validation. · ...

We are looking for a Project Manager with hands-on experience in Validation to provide full oversight of equipment qualification activities. · ...

We are looking for a Project Manager with hands-on experience in Validation to provide full oversight of equipment qualification activities. · This role will focus on Autoclaves, Fillers, and Partwashers within a regulated manufacturing environment. ...

+Job summary · We are looking for a Project Manager with hands-on experience in Validation to provide full oversight of equipment qualification activities. · +QualificationsBachelor's degree in Engineering, Life Sciences, or a related field. · 5+ years of experience in validation ...

Job Title: · Aseptic Facilities Manager · Overview: · The Aseptic Facilities Manager is a leadership role responsible for ensuring a safe, compliant, and highly efficient facility environment at an aseptic site in Raritan NJ supporting critical manufacturing operations. · Provide ...

We are seeking a Validation Specialist with more than five years of experience to support Utilities and Facilities Commissioning & Qualification (C&Q) activities for a biotech facility. · The ideal candidate has strong experience with electrical systems and regulated GMP environm ...

The Validation Specialist for Utilities and Facilities is responsible for ensuring the qualification and validation of critical utility systems and facility infrastructure in a GMP-regulated environment. · This includes HVAC systems water systems cleanrooms compressed gases and o ...

We are seeking a talented dedicated individual committed to work under the highest ethics standards for the position: Senior Computer System Validation (CSV) Specialist with expertise in Manufacturing Execution Systems (MES), specifically Syncade, to support a biologics manufactu ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: CQV Specialist – Media Fill (Aseptic Process). · ...