CQV Engineer: GMP Qualification & Validation Lead
Eurofins Agroscience Services North Carolina
Eurofins is seeking a hands-on CQV Engineer to support commissioning, qualification and validation for pharmaceutical and biotech facilities. You will author and execute IQ, OQ and PQ protocols, perform field verifications, and drive deviations and investigations in a GMP-regulated environment.
The role requires 2+ years GMP experience, ability to read P&IDs, strong technical writing, and willingness to work on site in Raleigh, NC with standard hours and occasional overtime; benefits include
#J-18808-Ljbffr- ...a hands-on commissioning, qualification and validation role with high growth potential... ...will work alongside our CQV Lead on facility, utility and equipment... ...for someone with real GMP experience who wants to... ...packages. ~ Work with client engineering and quality teams on site,...SuggestedFull timeContract workMonday to Friday
- ...Eurofins seeks a CQV Engineer to author and execute commissioning and qualification protocols for pharmaceutical and biotechnology... ...requiring minimum two years of GMP-regulated environment experience with direct involvement in validation activities. Responsibilities...Suggested
- ...Source is currently in search of a CQV Engineer for a pharmaceutical manufacturing client... ...conducting the Commissioning, Qualification, and Validation of Aseptic Formulation/Filling Equipment... ...HVAC, utilities, instrumentation, and GMP facility systems. ~ Working...SuggestedLong term contractVisa sponsorship
- ...Verista is seeking a Clean-in-Place (CIP) Engineer on site in Apex, NC, to lead commissioning and qualification for CIP systems within GMP environments. You will develop C&Q documentation, coordinate with design engineers, and ensure systems meet quality and safety standards...Suggested
- ...Indivior is seeking a Senior Validation Engineer to lead the development, implementation and continuous... .... The role requires expertise in qualification of equipment and processes, involvement... ...driving CAPA and change management within GMP environments. #J-18808-Ljbffr...Suggested
- ...Execution & Safety- Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on... ...- Bachelor’s degree (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant... ...industry- Essential experience in a GMP (Good Manufacturing Practice)...Full timeFor contractorsWorldwide
- ...currently hiring multiple Cleaning Validation Engineers to supports the execution and coordination... ...equipment and processes in GMP-regulated environments. This role is... ...industry leaders in Commissioning, Qualification, and Validation (CQV), we provide crucial services to the...Full timeTemporary workCurrently hiringFlexible hours
- ...global provider of system validation and lifecycle services... ...commissioning and qualification of computerized systems... .... Senior CQV Engineer (Cleaning Validation &... ...This consultant will lead validation activities... ...systems within a regulated GMP environment. The project...Daily paidContract workImmediate start
- ...seeking a detail-oriented Validation Specialist to support validation and qualification activities within a... ...Manufacturing Practices (GMP), and company quality... ...with Quality Assurance, Engineering, Manufacturing, Quality... ...qualification, and validation (CQV) activities for new or...Work at office
$111k - $219k
...services.Job TitleC&Q Validation Manager / Senior... ...Manager is responsible for leading teams and overseeing... ...firm as a leader in CQV services Create a strategic... ...of high-quality GMP Engineering services that meet... ...as well as individual qualifications, such as job-related...Full timeTemporary workLocal areaWork visa- Fresenius Kabi in the United States seeks a validation professional responsible for supporting operations through initial validation and requalification of equipment and systems. The role includes coordinating HEPA filter integrity testing, critical area airflow testing...For contractors
$102.9k - $175k
...We don’t settle until we give our best and know that we’re making a difference. As a Commissioning, Qualification, and Validation (CQV) Start-Up/Commissioning Engineer, you’ll join our collaborative team providing Commissioning and Start-Up services to clients in the Life...Full timeWork at office- ...Description: We are seeking an experienced Senior Validation Specialist to lead qualification and validation activities in a GMP-regulated environment. The ideal candidate... ...internal/external audits. Collaborate with Engineering, Quality Assurance, Manufacturing,...
$107.1k - $160.7k
...to become the world’s leading integrated design practice. Our architects, engineers, interior designers, consultants... ...The Commissioning and Validation role provides crucial... ..., stored in GMP conditions and distributed... ...systems which require qualification and validation for...Full timeTemporary workPart timeCasual workWork at officeLocal areaImmediate startFlexible hours$65 - $85 per hour
...seeking a Process Engineer - Aseptic Filling... ...Support to support a leading pharmaceutical... ...drug products, and GMP-regulated environments... ...commissioning, qualification, startup, and manufacturing... ..., Quality, Validation, Automation, and... ...Capital Projects, GMP, CQV, Commissioning,...Long term contract- ...Job Description Our Cary, NC CQV team is growing and looking to add additional CQV Engineer II resources to the team. \n \n In this role, you will lead commissioning, qualification, and validation (CQV) activities for pharmaceutical and biopharmaceutical facilities...Work at officeLocal area
- ...our clients that we're engineered for impact. This... ...operations, quality, validation, and external vendors... ...execution environments.Qualifications and Experience:Educational... ...processesExperience supporting CQV or validation-related... ..., CMMS systems, or GMP-aligned maintenance...For contractorsLocal area
- ...client is seeking experienced Validation Engineers/Validation Specialists to... ...project portfolio at a GMP manufacturing site in the greater... ...capable of independently leading validation activities with... ...development through qualification and, when applicable, decommissioning...Long term contractCasual workAfternoon shift
$150 per hour
...process/equipment engineer on the Drug Substance... ...commissioning and qualification over the next ~2... ...walkdowns. ~ Lead or supportcommissioning... ..., working with CQV and Automation (... ...facility. 3. NEED TO VALIDATE – Gaps / Open... ...and startup in a GMP environment ~...Contract workFor contractorsWork at officeLocal areaRelocationRelocation packageMonday to FridayShift workWeekend work$90k - $110k
...how it will be done.The GMP Operations Specialist is... ...Manufacturing, Quality, Engineering, Supply Chain, and Validation, they develop and implement... ...and industry standards. · Lead and facilitate training sessions... ..., interventions, gowning qualification assessments, and...Full timeWorldwide- ...seeking a Process Engineer - Aseptic Filling... ...Support to join a leading pharmaceutical manufacturing... ...projects within a GMP-regulated... ...startup, commissioning, qualification, and operational... ...Manufacturing, Validation, Automation, and... ...Commissioning, Qualification, CQV, Technology...Long term contract
- ...Upstream Process Equipment Engineers to support a large-... ...startup, commissioning, qualification, and operational readiness... ...systems within a GMP biologics environment.... ...Acceptance Testing) Support CQV (Commissioning, Qualification, and Validation) activities Interface...For contractorsWeekend work
- ...seeking an experienced Process Validation Engineer to support new... ...manufacturing projects within a sterile GMP environment. This role will... ...validation, technology transfer, and qualification activities for pre-filled... ...manufacturing processes. Lead Process Performance...Long term contract
- ...Downstream Process Equipment Engineers to support startup activities... ...process equipment within a GMP biopharmaceutical manufacturing... ...vendors, construction teams, CQV, operations, and QA teams to... ...and project requirements Qualifications ~ Bachelor’s degree in...For contractors
$90k - $110k
...GMP Operations SpecialistCAI is a professional services company... ...and industry standards.· Lead and facilitate training sessions... ...studies, interventions, gowning qualification assessments, and... ...Assurance, Quality Control, Engineering, and Manufacturing teams, to...Worldwide- ...Position Summary The Cleaning Validation Engineer oversees the development,... ...and contamination risk Lead CQV activities for CIP, COP,... ...align strategies Review GMP documentation (URS, FRS, P&... ...conductivity return) Equipment qualification (IQ/OQ/PQ) and utilities (...For contractors
$100k - $130k
...Our mission is to be the engine of innovation for genomic... ...Senior Engineer, Process Validation is responsible for leading & supporting internal and... ...process characterization and qualification spanning critical... ...aligned with FDA guidance, EU GMP Annex 15, and lifecycle...Full timeRemote workWork from homeFlexible hours- ...Guerbet seeks an experienced Utilities & Facilities Engineer to support clean utilities and plant utilities in a GMP-regulated pharma manufacturing environment. You... ...EHS, and Production to troubleshoot, maintain, and lead capital projects while driving continuous improvement...
- ...Alliance Biotech Solutions has multiple openings for Validation Engineers to support the execution and coordination of commissioning, qualification, and validation (CQV) activities for new and existing equipment within a GMP-regulated CDMO environment. These roles will...Full timeTemporary work
- ...Senior Engineer, Validation WHO WE ARE Indivior is a global pharmaceutical company... ...subject matter expert who leads the development,... ...perform requalification and qualification of equipment and or processes... ...compliant/validated state of all GMP equipment and systems. Interact...
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