Process Validation Engineer

Technical Source is currently in search of a Process Validation Engineer for our pharmaceutical manufacturing client in the Rocky Mount-Wilson, NC area. This is a long-term contract opportunity that operates on a rotating shift schedule. The ideal candidate for this position should have knowledge of validation duties, be mechanically inclined, and have...

Job Title: Validation Engineer/Process EngineerClient: IndiviorLocation: 8900 Capitol Blvd, Raleigh, NC-27616 Job Duties:Review, develop and execute validation lifecycle documents like FAT, SAT and qualification protocols for new equipment and existing equipment enhancements & upgrades for sterile filling, device assembly, and packaging equipment.Develop...

Description Hughes Engineering & Consulting is an exciting, fast-growing company focused on Process Engineering, Project Engineering, Project Management and CQV solutions for the pharmaceutical industry. We offer great benefits, and exciting challenges for both career development as well as personal leadership development. Company Culture Guidelines &...

About Us: Design Group operates from more than 45 offices in the United States and India, providing engineering, consulting and technical services for the world's leading companies in the food and beverage, life sciences, advanced technology, industrial and other market sectors. Our nearly 1,500 technical and engineering experts have direct industry...

About Us: Design Group operates from more than 45 offices in the United States and India, providing engineering, consulting and technical services for the world's leading companies in the food and beverage, life sciences, advanced technology, industrial and other market sectors. Our nearly 1,500 technical and engineering experts have direct industry...

The Cleaning Validation Engineer is responsible for cleaning and process engineering and validation in the biotech and pharmaceutical industries. This individual will generate, execute, and report on testing for multiple phases of commissioning and qualification. The position involves post cleaning validation monitoring, cleaning cycle development and...

Validation Engineer (MES) Location: Durham, North Carolina Provide computer system validation support for a leading contract development and manufacturing organization (CDMO) specializing in the production of biologics and advanced therapies. We are seeking a flexible and adaptable Validation Engineer (CSV Lead) to represent our team in North Carolina. In...

Job DescriptionJob DescriptionValspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec's mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle...

Validation LeadLocation: Raleigh, NCWorking Situation: OnsiteA global speciality pharmaceutical company is looking to bring on a Validation Lead to support the global quality organization. You will be supporting tech transfer and validation activities while also working cross-functionally to support all GxP related issues at the Raleigh, NC site.The...

Validation LeadLocation: Raleigh, NCWorking Situation: OnsiteA global speciality pharmaceutical company is looking to bring on a Validation Lead to support the global quality organization. You will be supporting tech transfer and validation activities while also working cross-functionally to support all GxP related issues at the Raleigh, NC site.The...

Validation LeadLocation: Raleigh, NCWorking Situation: OnsiteA global speciality pharmaceutical company is looking to bring on a Validation Lead to support the global quality organization. You will be supporting tech transfer and validation activities while also working cross-functionally to support all GxP related issues at the Raleigh, NC site.The...

Raleigh, North Carolina / Southeast / Full Time Position Description: The CQV Engineer develops the documentation to support Commissioning, Qualifications, and Validation. These people are responsible for protocol writing and execution, field verification, and development of summary reports at the client site. Other responsibilities include planning /...

As a Process engineer, you will mechanically troubleshoot, support identification and implementation of process improvements, system design, capital project support, and investigation support. You will also ensure all documentation deliverables are generated and develop new processes and/or optimize existing ones.  Responsibilities: Acts as the SME for...

This position is responsible for supporting the validation and quality engineering of various systems across the pharmaceutical, biopharmaceutical, and medical device manufacturing areas and assure the equipment/system and validation programs are compliant with client’s global/site standards and industry practices.Responsibilities and Duties: Located in...

This position is responsible for supporting the validation and quality engineering of various systems across the pharmaceutical, biopharmaceutical, and medical device manufacturing areas and assure the equipment/system and validation programs are compliant with client’s global/site standards and industry practices.Responsibilities and Duties: Located in...

Job Description Client: Brevitas Corp. Our Global Company, Brevitas Corp., is dedicated to helping organizations achieve tangible results and lasting improvements via successful project delivery, continuous process improvement and effective management of change. We serve businesses in a wide range of industries including Pharmaceuticals, Food & Beverage,...

Job Description At IPS, you will apply your knowledge, skills, and passion to make a difference in the lives of people by solving complex challenges related to pharmaceutical, biotech, and animal health research and manufacturing facilities. We are looking for a dedicated Lead Process Engineer to join our talented team at our office located in our...

Responsibilities: Installation and startup testing of new equipment (generation, execution, and close out of engineering test plans) Ownership of system P&IDs - responsible for engineering review, walk-downs, redlines & system changes. Generation, review, and approval of engineering lifecycle documentation for assigned systems. Review, approval, and...

GRAIL is a healthcare company whose mission is to detect cancer early, when it can be cured. GRAIL is focused on alleviating the global burden of cancer by developing pioneering technology to detect and identify multiple deadly cancer types early. The company is using the power of next-generation sequencing, population-scale clinical studies, and...

Overview: At Page, we promise design that makes lives better. Were actively seeking talented people to join an empowered employee environment. Page provides architecture, engineering, interiors and consulting services on large, complex projects around the world. We credit the success of our projects that build communities to the global diversity of our...