CQV Engineer - Pasadena

A large pharmaceutical manufacturer is seeking an onsite CQV Engineer to support a capital facilities project. · ...

The client needs someone with Facilities CQV experience including EMPQ (environmental monitoring performance qualification), Vessel IQ/OQ/PQ including mixing and temp mapping. · ...

We are hiring on behalf of a client for a highly autonomous CQV Engineer to support capital projects within the biopharmaceutical industry. · This is a hands-on, on-site role requiring an experienced professional who can independently manage and execute Commissioning, Qualificati ...

We are looking for CQV Engineers to support our LA area client's project. The role requires experience in executing CQV protocols within pharmaceutical facilities and written and executed protocols and protocol final reports. · ...

We are hiring on behalf of a client for a highly autonomous CQV Engineer to support capital projects within the biopharmaceutical industry. · Requirements:Independently manage and execute CQV activities for capital projects · Lead CQV project execution and coordinate with cross-f ...

+Job Title: · CQV Engineer (Biopharma) · +We are hiring on behalf of a client for a highly autonomous CQV Engineer to support capital projects within the biopharmaceutical industry. · ...

We are seeking experienced CQV Engineers to support a large-scale biotech/pharma capital project in Southern California.The role will focus on qualification of cleanroom facilities and manufacturing-scale process equipment in an active construction and GMP environment. · ...

We are hiring on behalf of a client for a highly autonomous CQV Engineer to support capital projects within the biopharmaceutical industry. · Independently manage and execute CQV activities for capital projects · Lead CQV project execution and coordinate with cross-functional sta ...

+The client needs someone with Facilities CQV experience including EMPQ (environmental monitoring performance qualification), Vessel IQ/OQ/PQ including mixing and temp mapping. · ...

We are seeking experienced CQV Engineers to support a large-scale biotech/pharma capital project in Southern California.The role will focus on qualification of cleanroom facilities and manufacturing-scale process equipment in an active construction and GMP environment. · ...

We offer an opportunity to help support our teams of industry subject matter experts and thought leaders while consulting with some of the biggest companies in the Life Sciences industry. · Provide validation support (IQ, OQ, PQ) for process vessels · Installation Qualification<o ...

A large pharmaceutical manufacturer is seeking an onsite CQV Engineer to support a capital facilities project. · ...

A large pharmaceutical company in Los Angeles is in immediate need of a CQV Engineer. The client needs someone with Facilities CQV experience including EMPO, Vessel IOV and IOPQ including mixing and temp mapping. · ...

The client needs someone with Facilities CQV experience including EMPO, Vessel IOV and IOPQ including mixing and temp mapping. · BS degree minimum1-4 years of Validation Engineering experience in pharmaceutical industry ...

A large pharmaceutical company in Los Angeles is seeking a CQV Engineer for a 12-month project. The role requires facilities CQV experience including EMPO, Vessel IOV and IOPQ including mixing and temp mapping. · ...

The client needs someone with Facilities CQV experience including EMPO, Vessel IOV and IOPQ including mixing and temp mapping. · Manage Installation and Operational CommissioningAuthor and Approve Execution Function Testing BOM Updates PM Generation Asset Lifecycle Drawing Update ...

CQV engineer with experience in large-scale equipment CQV and biopharma industry required. Must have expertise in authoring CQV lifecycle documentation and self-manage CQV projects independently. · ...

CQV Engineer · Lead qualification of cleanroom facilities and large-scale manufacturing process equipment including centrifuges and filter presses. · Author execute and close validation protocols and final reports with minimal oversight. · Conduct construction walks pre-check P&I ...

Lead qualification of cleanroom facilities and large-scale manufacturing process equipment. Author validation protocols and final reports with minimal oversight. · ...

++We are seeking a CQV / Validation Engineer to support commissioning qualification and validation activities for pharmaceutical manufacturing systems equipment and utilities in a GMP regulated environment. · ++Develop and execute DQ IQ OQ and PQ protocols for manufacturing equip ...