LabWare LIMS Validation Specialist - Onsite GMP Lab
Radiant Systems, Inc.
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 laboratory workflows and working closely with quality and validation teams. The role requires hands-on validation document generation and collaboration with various stakeholders. A solid background in regulatory compliance and LIMS configuration is crucial for success. #J-18808-Ljbffr Radiant Systems Inc
$80 - $90 per hour
...Title: LabWare LIMS Validation Specialist Location: Thousand Oaks, CA 91320 (Onsite) Duration: 9+ Months (Possible extension) Job Summary LabWare LIMS Configuration... ...support the LabWare 8 upgrade for a US based GMP laboratory site. This role will lead a...SuggestedHourly payFull timeTemporary work$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... ...Specialist to support a LabWare 8 upgrade for a GMP laboratory site.This role will lead a dedicated workstream...SuggestedHourly payContract work- ...LabWare Lims Validation Specialist Greetings, I am seeking an experienced LabWare Lims Validation Specialist... ...a LabWare 8 upgrade for a US-based Gmp laboratory site in Ca. This role will... ...project and strong liaison with onsite Smes. 9+ month Onsite Contract role...SuggestedContract work
- A leading consulting firm located in Thousand Oaks seeks a Validation Engineer to ensure compliance with cold storage validations and computer... ...skills. This role requires local candidates who can work onsite and support ad hoc laboratory operations projects. #J-18808-Ljbffr...SuggestedLocal area
- 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...SuggestedContract work1 day per week
- Job Title: Senior C&Q Validation Engineer - GMP Analytical & Process Equipment- (JP15147) Location: Thousand Oaks, CA. 91320 (Hybrid) Employment Type: Contract Business Unit: Engineering Systems Duration: 1+ year (with likely extensions and/or conversion to permanent...Permanent employmentContract workLocal areaRelocation
$60 - $70 per hour
A consulting firm in life sciences seeks a Senior C&Q Validation Engineer for leading commissioning and qualification activities on GMP analytical and process equipment. Candidates should have relevant education and experience in pharmaceutical or biotech settings. The...Contract work- A leading global biotechnology company seeks an Engineer for Life Cycle Management of GMP Test Methods. This hybrid role involves supporting senior engineers, developing test methods, and ensuring compliance with industry standards. Ideal candidates have strong analytical...
- ...Principal (DeltaV/PLC/Scada), Biopharma/GMP - (JP13780) Location: Thousand Oaks... ...GMP Manufacturing facility experience Onsite position 3-5 years industry... ...detailed design, engineering, commissioning, validation, and project execution, as it relates to...Long term contractContract work
- ...control engineering and troubleshooting with GMP biopharmaceutical production facility... ...development, detailed design, engineering and validation documentation and project execution. ~... ...Operational Support including: 24 x 7 Onsite/On Call: Day to Day Operational Support...Work experience placementWork at office
$36 - $41 per hour
...s Degree in a scientific or engineering discipline and involves supporting process development and technology transfer projects in a GMP environment. Candidates with strong analytical skills and experience in project management are desired. Competitive pay rate of $36 -...Contract work- ...Senior Automation Engineer - DeltaV DCS / Rockwell PLC & SCADA (GMP Biopharma Capital Projects) Job ID JP15356 Location Thousand... ...case development, detailed design, engineering, commissioning, validation, and project execution as it relates to Plant Automation and process...Permanent employmentContract work
$60 - $70 per hour
...qualification actions/documentation versus project(s) timelines. Author/evaluate qualification/validation protocols including DQ, IQ, OQ, FT, PQ protocols and final reports for new or modified GMP utilities, facilities, and process equipment. Execute DQ, IQ, OQ, FT, PQ protocols,...Contract work- Job Details Job Title: Validation Engineer - Cold Storage & Analytical Equipment - (JP14626)... ...Only qualified candidates need apply. Fully onsite. Local candidates only Overview 3 Key... ...Analytical Equipment experience Preferably Lab Ops/Equipment Background Drafting...Permanent employmentContract workLocal area
- ...biopharmaceutical processes, and requires a strong engineering background. This position is contract-based with opportunities for extensions and permanent placement, ideally suited for motivated candidates with experience in GMP environments. #J-18808-Ljbffr 3key Consulting, Inc.Permanent employmentContract work
- ...clinical supply, requiring strong expertise in various automation platforms and project management. Candidates must have significant experience in GMP facilities and life sciences to be successful in delivering complex automation projects. #J-18808-Ljbffr 3key Consulting, Inc.Long term contract
- ...Candidates must have experience with Emerson Delta-V DCS and Rockwell Automation systems, along with a background in life sciences. This onsite position supports both clinical and commercial plant automation initiatives for a duration of 3 years with the potential for full-...Full time
- ...firm is looking for an Engineer to support equipment and method validation efforts in Thousand Oaks, CA. The role involves working with... ...with experience in project support. This position will require onsite presence at least twice a week and offers a contract duration of...Contract work
- ...hybrid in Thousand Oaks, CA, requires expertise in medical device engineering standards, technical writing, and hands-on testing in a lab environment. The role promises rich collaboration opportunities and responsibilities in a fast-paced project environment, ideal for...Contract work
- A leading global biopharmaceutical company is seeking an Engineer for a consulting engagement. The role focuses on developing and supporting technical documentation related to container closure integrity (CCI) testing with a strong emphasis on collaboration and technical...
- ...1+ years (with possible extensions) Rate: $60 - $70/hour W2 Posting Date: 08/30/2023 Notes: Only qualified candidates need apply. Onsite 8:00 AM - 5:00 PM with some flexibility to work remotely. Job Description 3 Key Consulting is recruiting a Manufacturing and Clinical...Contract workRemote work
- ...side/ mathematics. NOT LOOKING for quality lab/ bench top/ science work. The job seeker... ...Automation and Equipment Systems (QRAES) to validate equipment design while minimizing project... ...oil refinery/ mechanical Troubleshooting GMP Manufacturing process equipment. Statistical...Contract workWork experience placement
$38 - $42 per hour
...capabilities, as well as assist in the process validation and technology transfer of multiple... ...characterization studies and other experiments at the lab scale and production scale to generate... ...systems and Drug Product Manufacturing (GMP). Demonstrated ability to use...Contract workWork experience placementLocal areaWork from homeFlexible hours2 days per week1 day per week- ...statistical methods to derive actionable insights and recommendations. Support design changes by leading testing efforts to assess and validate proposed modifications. Participate in scale‑up, global launch, and continuous improvement of drug delivery devices. Collaborate...Contract work
- 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...Full time
- Be visionary Teledyne Technologies Incorporated provides enabling technologies for industrial growth markets that require advanced technology and high reliability. These markets include aerospace and defense, factory automation, air and water quality environmental...Minimum wageWork experience placementWork at officeLocal area
- ...24/23 Notes: Only qualified candidates need apply. Will not be onsite every day, and will depend on project (80% of time can be remote... ...exploring technologies in partnership with site PD, NPI lead, Validation Engineering and Project Managers Top Must Have Skill Sets: Engineering...Permanent employmentContract workRemote work
- ...automation background in design, installation, programming, and validation of automated processes. ~2+ years combined experience with... ...references from previous 2 positions Reluctance to relocate or be onsite Interview Process Virtual interviews via webex. I will...Relocation
$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- A leading consulting firm in biotechnology is seeking a Senior Software Engineer in Thousand Oaks, CA, to develop process control applications. The ideal candidate will have over 5 years of experience in automation, particularly within regulated environments. Responsibilities...Permanent employmentPlacement year
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