QA Validation Specialist - GMP/CSV Focus
USA - 3390 Baxalta U.S., Inc.
Takeda is seeking a Quality Assurance Validation Associate in Thousand Oaks to oversee validation deliverables and change controls, ensuring GMP and GxP compliance across facilities, utilities, equipment, and computerized systems. The role emphasizes risk assessment, traceability, and collaboration with cross-functional teams to support regulatory submissions and manufacturing readiness. #J-18808-Ljbffr USA - 3390 Baxalta U.S., Inc.
- Katalyst CRO in Thousand Oaks, CA, seeks a Validation Lead to drive Labware LIMS 8 validation projects and ensure GXP compliance... ...validation testing activities. The role emphasizes CSV, GAMP 5, and enterprise GMP systems, with a proactive approach to risk, change control...Suggested
- ...079Remote50% RemoteResponsibilities:Lead validation activities for Labware LIMS 8 implementationAuthor... ...documentationEnsure compliance with GXP, CSV, and regulatory standardsSupport audits,... ...)Computer System Validation (CSV)GXP / GMP EnvironmentGAMP 5 & Regulatory...Suggested
- Amgen in Thousand Oaks seeks a Specialist Manufacturing - Cleaning Validation for the Drug Substance Supply, supporting multi-product biologics manufacturing. You will own validation requirements, lead cross-functional projects from planning to execution, and provide technical...Suggested
- ...materials and components. The role requires handling heavy drums, maintaining training records, and performing quality reviews within a GMP environment. Training can be provided for GMP exposure; ADA accommodations available as needed. The candidate will contribute to...Suggested
- ...pounds, pass a vision assessment, and work in clean room sampling areas. Training on GMP will be provided; prior GMP is a plus. Qualifications include high school diploma with 2 years QA experience or an Associate's + 6 months, or a Bachelor’s degree. #J-18808-Ljbffr...Suggested
- ...Oaks seeks a Sr. Associate Quality Assurance to support the Plant QA organization, providing daily oversight of Drug Product... ...regulatory requirements. Duties include electronic batch review, GMP document revision, maintenance work order approvals, and evaluating...Shift work
- ...Job Title Lead validation activities for Labware LIMS 8 implementation Author and review... ...Ensure compliance with GXP, CSV, and regulatory standards Support audits... ...Computer System Validation (CSV) GXP / GMP Environment GAMP 5 & Regulatory Compliance...
$104.29k - $141.09k
...toughest diseases. With our focus on four therapeutic areas -Oncology... ...the Drug Product QA Specialist provides Quality oversight to... ...such as process and product validation.Provides quality expertise and... ...utility monitoring systems within GMP manufacturing environments Excellent...Full timeFlexible hours$71.8k - $112.86k
...role: As a Quality Assurance Validation Associate, you will work as part... ...This position will typically focus on disciplines related to facilities... ...implement all the applicable QA requirements. Participate in... ...-related issues, including GMP regulations Assess and approve...Full timeLocal areaShift work- ...Quality Assurance Validation Specialist Position Summary Location: Thousand Oaks, California —... ...accuracy, completeness, consistency, and GMP compliance. Provide quality review and... ...(PQ) Computer System Validation (CSV) Validation maintenance packages System...Full timeFor contractors
$116k - $182.27k
...supports the operations through the initial qualification to validation maintenance of equipment, systems, facilities, and utilities.... ...(PQ) / Cleaning Validation (CV), and Validation Maintenance. Focused on right first-time execution and continuous improvement.How you...Minimum wageFor contractorsLocal areaShift work$104.8k - $192.2k
...regulatory requirements. Stable and scalable enterprise integrations. What we offer you At EY, we’ll develop you with future-focused skills and equip you with world-class experiences. We’ll empower you in a flexible environment, and fuel you and your extraordinary...For contractorsSummer holidayFlexible hours- ...Responsibilities • Design advanced test methodologies to validate new products for functional completeness, performance, and system... ...hardware verification or product test engineering, with a strong focus on high-speed digital products and complex system level validation...
$100.45k - $135.9k
...toughest diseases. With our focus on four therapeutic areas -Oncology... ...your career.Quality Control Specialist, MicrobiologyWhat you will... ...in a fast-paced, flexible GMP laboratory.Ability to generate... ...Ability to generate and document validation protocols and reports....Full timeContract workWork experience placementFlexible hoursWeekend work- ...for the Thermal Engineering Lab Testing & Equipment Qualification (GMP) at our Thousand Oaks, CA facility. This contract role supports... ...budgets and inventory, schedule activities, and collaborate with R&D, QA/QC, supply chain, and regulatory teams to ensure compliant...Contract work
$26 - $47.5 per hour
Job Title: Validation Engineer (VE) Summer/Fall Co-Op (June-Dec '27) Posting Start Date: 8/18/26 Job Location(s): Newbury Park If you are... ...Skyworks, you will find a fast-paced environment with a strong focus on global collaboration, minimal layers of management, and the...Hourly paySummer workInternshipWork at office- Scorpion Therapeutics seeks a Quality Assurance Validation Associate to lead oversight of validation deliverables, ensuring compliance with regulatory standards and internal SOPs. You will review and approve validation documents across facilities, utilities, equipment,...
- ...Engineer - Thermal Engineering Lab Testing & Equipment Qualification (GMP) - (JP15950) Thousand Oaks, CA Biotech/Pharmaceutical Job Title:... ...with cross-functional teams (i.e. Research and Development, QA/QC, Supply Chain, Maintenance, Manufacturing, Regulatory) on protocol...Permanent employmentContract work
- Inc. (Vti) is seeking an experienced Quality Assurance Validation Specialist to provide quality oversight for pharmaceutical and biopharmaceutical... ..., manufacturing equipment, instruments, and computer systems, with a focus on data integrity and #J-18808-Ljbffr Inc. (Vti)
- 3 Key Consulting, Inc. is hiring for an Artwork Quality Control & Human Factors Prototype Specialist - Combination Products in Thousand Oaks, CA. This contract role supports QC and inspection of Instructional Design artwork deliverables and builds physical study stimuli...Contract work
- ...seeks a Drug Product Quality Assurance Specialist to provide quality oversight for aseptic... ...inspection areas, utilities, and nonroutine validation activities Participate in internal... ...environmental monitoring, and utility systems in GMP manufacturing Excellent written and...
$90k - $110k
...supporting and improving manufacturing processes with a primary focus on CNC machining operations, setup optimization, tooling,... ...processes, including machine setup optimization, tooling selection and validation, process development, troubleshooting, root cause...Full timeContract work- Amgen’s Thousand Oaks site seeks a Drug Product Quality Assurance Specialist to provide quality oversight for aseptic manufacturing and inspection areas. You will ensure compliance with cGMP, quality systems, and regulatory expectations while partnering with Manufacturing...Flexible hours
$98.24k - $135.08k
...Advisory ( // Sensing is what we do. In fact, our name Sensata comes from the Latin word sensate for ‘those gifted with sense’. Our focus on sensing is also reflected in our logo, which spells Sensata in Braille. Sensata Technologies is a global industrial technology...Full timeTemporary workWork experience placementWork at officeLocal areaFlexible hours- ...the world's toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation... ...for operation and maintenance, equipment validation, and support regulatory inspections and... ...engineering and troubleshooting with GMP biopharmaceutical production facility equipment...Work at officeRemote workFlexible hours
- Skyworks Solutions, Inc. in Newbury Park, CA is seeking a Validation Engineer Co-op for 6 months (June-December 2027) to support high-volume PA products and sub-systems for cellular handset applications. You will assist setup tests, gather data, and work with design engineers...Summer work
$162k - $239.76k
...that have moved into volume production10 years experience with RF/Mixed-Signal/Sipho IC test; specifically, in test engineering with focus on hardware and software design, yield improvement, test time reduction and manufacturing process improvementsSkilled in software...Permanent employmentFull timeInternshipWork from home$81.6k - $129.6k
...We are the global test and automation specialists powering next-generation technologies through... ...architecture design analysis and validation of advanced semiconductor test systems across... ...Engineering with a thermal sciences focus. Experience with semiconductor test equipment...Full timeLocal areaRelocationFlexible hours- ...resolving and preventing issues quickly when product stops occur.• Provide functional and technical support within the assigned area of focus as well as the organization as required to support goals.• Actively participate in design, definition, and manufacturing of...Permanent employmentH1bLocal areaImmediate startVisa sponsorshipRelocation package
- ...production floor over sitting at a desk, this is the opportunity for you. You will step right in to support our manufacturing operations, focusing on safety, quality, delivery, and cost. We need someone who is adaptable, eager to get their hands dirty, and ready to drive...
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to QA Validation Specialist - GMP/CSV Focus. Be the first to apply!
- qa technician Thousand Oaks, CA
- qa Thousand Oaks, CA
- quality assurance team leader Thousand Oaks, CA
- quality assurance Thousand Oaks, CA
- quality assurance representative Thousand Oaks, CA
- work from home qa testing Thousand Oaks, CA
- lead qa Thousand Oaks, CA
- quality assurance documentation specialist
- sr. quality assurance specialist
- senior quality assurance specialist




