Validation Specialist
Creative Solutions Services, LLC
Responsibilities Lead validation activities for Labware LIMS 8 implementation Author and review IQ/OQ/PQ, RTM, and validation documentation Ensure compliance with GXP, CSV, and regulatory standards Support audits, inspections, and validation testing activities. Required Skills Labware LIMS (Labware 8 Preferred) Computer System Validation (CSV) GXP / GMP Environment GAMP 5 & Regulatory Compliance IQ / OQ / PQ Documentation Requirements Traceability Matrix (RTM) Validation Strategy & Execution Audit Readiness & Inspection Support Deviation, CAPA & Change Control Management Laboratory Systems & Enterprise GMP Systems Validation. #J-18808-Ljbffr
- Veg Group seeks a Validation Lifecycle & Periodic Review Specialist in California to maintain validated systems throughout their lifecycle. This hybrid role involves supporting validation activities for GMP equipment and systems, ensuring compliance and suitability. The...Suggested
- Validation Lifecycle & Periodic Review Specialist Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas...Suggested
$90 - $100 per hour
Job Title LabWare LIMS Validation Specialist (Onsite role) Contact Please let me know if you are interested or anyone who might be interested. Client Major Pharmaceutical Client Position Details Position: LabWare LIMS Validation Specialist (Onsite role) Duration: 9+...SuggestedHourly payContract work- Radiant Systems Inc is seeking a LabWare LIMS Validation Specialist for an onsite role in Thousand Oaks, California. This position involves configuring LabWare LIMS and ensuring compliance with GMP standards. The ideal candidate will have proven experience in implementing...Suggested
- US Data Management, LLC is seeking a Validation Analyst to support a PAS-X upgrade project in Thousand Oaks, CA. This role includes executing validation activities under the direction of the lead validation resource and ensuring compliance with GAMP 5 principles. The ideal...SuggestedFull time
- Takeda Pharmaceuticals International GmbH is seeking a Validation Engineer in Thousand Oaks, CA. The role involves leading validation activities, managing project timelines, and ensuring compliance with regulations. The ideal candidate will have more than 10 years of experience...
$60 - $65 per hour
Validation Engineer Senior Onsite Primarily responsible for leading and/or executing commissioning and qualification activities on new or modified GMP analytical and process equipment, utilities, and facilities. Responsibilities include generating, reviewing, and executing...Hourly pay$116k - $182.27k
Job Description This position supports the operations through the initial qualification to validation maintenance of equipment, systems, facilities, and utilities. Responsible and accountable for performing activities such as Cycle Development (CD), Design Qualification...Minimum wageFull timeTemporary workFor contractorsLocal areaShift work- A consulting firm in biotech engineering is hiring a Validation Engineer for a 1+ year contract role in Thousand Oaks, CA. The position focuses on commissioning and qualification protocols in a GMP environment. Ideal candidates will have relevant degrees and experience...Hourly payContract work
- Job Title: Validation Engineer, Biopharma, Hybrid (once/week onsite) - (JP10478) Location: Thousand Oaks, CA (Hybrid, once a week on site) Employment Type: Contract Business Unit: A utoTouch Platform Team Duration: 1+ years with likely extensions Posting Date: 06/24/20...Contract work1 day per week
- A leading consulting firm located in Thousand Oaks seeks a Validation Engineer to ensure compliance with cold storage validations and computer validation for analytical instruments. The ideal candidate should have a Master's or relevant Bachelor's degree, with experience...Local area
$75 - $85 per hour
Job Function: Validation Analyst Location: Thousand Oaks, CA About USDM USDM Life Sciences is a premier consulting company with 20+ years of experience assisting heavily regulated biotech, medical device, and pharmaceutical companies with their GxP technologies to accelerate...Hourly payFull timeContract workTemporary workPart timeWork at officeHome officeShift work- Validation Engineer job at Planet Group. Thousand Oaks, CA. Target PR Range: 40-50/hr *Depending on experience Experience needed: Cold Storage Validation Experience Analytical Equipment experience Preferably Lab Ops/Equipment Background Drafting Documents Primarily responsible...
- Job Details Job Title: Validation Engineer - Cold Storage & Analytical Equipment - (JP14626) Location: Thousand Oaks, CA. 91320 Employment Type: Contract Business Unit: Final Product Technologies Development Duration: 12+ months (with likely extensions and/or conversion...Permanent employmentContract workLocal area
- Job Title: Validation & Verification Engineer, Medical Drug Delivery Device (Hybrid) - (JP10785) Location: Thousand Oaks, CA (Hybrid, once a week or once bi-weekly on site) Employment Type: Contract to Hire Business Unit: AutoTouch Drug Delivery Device - Platform Team...Permanent employmentContract work1 day per week
- Overview Job Title: Validation Engineer, Biotech Facilities & Engineering (JP13959) Location: Thousand Oaks, CA. 91320 Business Unit: F&E Drug Product Supply Employment Type: Contract Duration: 1+ years with possible extension or conversion to FTE Rate: $42 - $52/hour...Contract work
$30.53 - $39.66 per hour
A leading semiconductor company in California seeks an RF Engineering Technician to support their High Power RF Group. The role involves conducting RF testing in a lab environment, collaborating on new designs, and ensuring accurate data collection. Candidates must have...Hourly pay- A medical consulting firm is looking for an Engineer to support equipment and method validation efforts in Thousand Oaks, CA. The role involves working with senior staff on automation projects, executing validation protocols, and conducting engineering assessments in a...Contract work
- A leading consulting firm is seeking an Engineer for a medical device and equipment validation role located in Thousand Oaks, California. This hybrid position will involve supporting senior engineers in the design and delivery of automation projects. Ideal candidates will...Contract work
- Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in ...Flexible hours
- Amgen SA in Thousand Oaks is seeking a Synthetics Supply Manufacturing Engineer to join the Drug Substance and Drug Product facilities. In this role, you will lead small molecule API production while collaborating with various teams to advance early-phase synthetic pipeline...Flexible hours
- ...Requirements Specifications (URS). Suggest design modifications to address risks and design in quality and safety. Oversee development of validation protocols in line with CQP, Automation Systems Delivery SOPs, and standards. Act as a liaison between Engineering and...Contract workFor contractorsWork experience placement
- Overview Job Title: Senior Engineer, MCS/Manufacturing & Clinical Supply - (JP11756) Location: Thousand Oaks, CA. 91320 Hybrid Business Unit: F&E Drug Product Supply Employment Type: Contract Duration: 1+ years (with possible extensions) Rate: $60 - $70/hour W2 Posting ...Contract workRemote work
$38 - $42 per hour
...then translation of requirements into process equipment/system design, specification and supporting the construction, startup, and validation of equipment. Be individually accountable for the verification deliverables. Assist in the identification of critical quality...Full timeContract workFor contractorsWork experience placementRemote work- .... Develop the commissioning strategy based on the URS and Quality Risk Assessment for Automation and Equipment Systems (QRAES) to validate equipment design while minimizing project cost and schedule impact (risk-based approach). Oversee development of validation protocols...Contract workWork experience placement
- ...development for commercial drug product processing in areas such as sterile processing, process characterization, tech transfer, and validation. Collaborate with manufacturing and support functions to provide coordinated support for commercial drug product manufacturing...Permanent employmentContract work
- Initial Therapeutics, Inc. is seeking a Synthetics Supply Manufacturing Engineer to join our team in Thousand Oaks, California. You will play a vital role in advancing our early phase synthetic pipeline, executing small molecule active pharmaceutical ingredient (API) production...
$60 - $65 per hour
Crystal Equation Corporation in Thousand Oaks is seeking a Senior Validation Engineer to lead the commissioning and qualification activities for new or modified GMP analytical and process equipment. The ideal candidate will possess demonstrable experience within a pharmaceutical...Hourly pay- Veg Group is seeking a Validation Lifecycle & Periodic Review Program Manager to lead and manage validation lifecycle and periodic review programs for various clients in regulated industries. This role plays a critical part in ensuring compliance with GMP and quality standards...
- Validation & Engineering Group, Inc. is seeking a Senior Validation Lifecycle & Periodic Review Specialist. This hybrid role focuses on maintaining validated systems in pharmaceuticals and biotechnology environments. The ideal candidate will have over 5 years of relevant...
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