Regional Manager of Southeast CQV Services - Raleigh/Durham Area, NC

We are hiring CQV Engineers (I, II, III, IV) of varying experience responsible for the commissioning, qualification and validation for facilities utilities and process equipment in the pharmaceutical and biotech industries. · ...

The Commissioning, Qualification, and Validation Engineer II report directly to the Team Leader Manager or Director of the CQV Team depending on the organizational structure. Up to 100 travel may be required. · ...

Exciting client side opportunities in the Raleigh/Durham area for those looking to take the next big step in their career within the Life Sciences industry. · PM Group is currently engaged in the delivery of multiple Life Science projects in the USA. · You will be on-site executi ...

We are seeking a highly motivated and experienced CQV Engineer to join our team in Holly Springs, North Carolina. · The CQV Engineer will be responsible for leading commissioning, qualification, and validation activities for new and existing pharmaceutical facilities and equipmen ...

The CQV Engineer II report directly to the Team Leader, Manager, or Director of the CQV Team. These positions are exempt. Up to 100% travel may be required. · CQV Engineers take a proactive role in supporting CQV projects and in providing client support..Performs commissioning, q ...

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. · ...

We are seeking an experienced CQV Validation Engineer to join our team in Cary, NC. The ideal candidate will have a strong background in the pharmaceutical or biotech industry and 5–8 years of experience in commissioning, qualification, and validation of equipment, systems, and p ...

The Director of Commissioning Qualification and Validation CQV/CSV projects while driving business development initiatives This role manages a team of senior junior resources focusing on project execution building nurturing client relationships to promote Kymanox services · ...

The Commissioning Qualification and Validation Engineer II report directly to the Team Leader Manager or Director of the CQV Team depending on the organizational structure. · CQV Engineers take a proactive role in supporting CQV projects and in providing client support. They buil ...

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 ...

We don't settle until we give our best and know that we're making a difference. As a Commissioning Qualification and Validation CQV Engineer you'll join our collaborative team providing CQV support to clients that manufacture GMP products on a consistent basis in conjunction with ...

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. · Serve as the Utilitie ...

Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. · We are seeking a highly motivated and detail-oriented GMP Equipment Validation Engineer to support C ...

The Commissioning, Qualification, and Validation Engineer II reports directly to the Team Leader, Manager, or Director of the CQV Team. · In-depth understanding of cGMPs and pharmaceutical and biopharmaceutical unit operations. · ...

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. · ...

The Project Engineer is a fully billable role that will work collaboratively with clients, vendors, contractors, and other Team Members to support projects related to biomanufacturing across the entire engineering lifecycle. · ...

We are looking for a dedicated Construction Intern to join our talented team at our office in Cary, North Carolina.At IPS, we are global leaders in developing innovative solutions for the consulting architecture engineering project controls procurement construction management and ...

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 ...