NewManager, Project Engineering L3Harris TechnologiesManager, Project EngineeringCanoga Park, CA$127,500–$236,500 / yearIn this role, the selected candidate will provide technical direction and oversight to team leads, driving stronger program execution and greater consistency across all programs within the Los Angeles and (other site) Project Engineering teams. L3Harris is seeking an experienced, highly organized, and detail-oriented Project Engineering Manager to lead a team of technical leaders across multiple Missile Propulsion programs.
ERP Program Manager (Oracle E-Business Suite EBS | SIOP | Supply Chain) Johnson Service GroupERP Program Manager (Oracle E-Business Suite EBS | SIOP | Supply Chain)Oxnard, CAJohnson Service Group (JSG) is seeking an experienced ERP Program Manager (Oracle E-Business Suite) EBS | SIOP | Supply Chain) for a direct hire opportunity with a leading aircraft manufacturer in Oxnard, CA . The ideal candidate does not need to be an Oracle functional expert but should understand how Oracle ERP modules support manufacturing operations and what is required for a successful implementation.
NewValidation Lifecycle & Periodic Review Program Manager Validation & Engineering Group, IncValidation Lifecycle & Periodic Review Program ManagerThousand Oaks, CAJob Description 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: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. In addition to providing program leadership and client interface responsibilities, the successful candidate will be expected to actively support execution activities as needed, including review assessments, technical evaluations, report generation, and other validation lifecycle deliverables.
NewReady Mix Plant Manager CalPortlandReady Mix Plant ManagerCanoga Park, CA$75,000–$105,000 / yearThe Ready-Mix Plant Manager works closely with the batch men and drivers in overseeing ready-mix plant production, operations and site facilities. This individual is responsible for planning and budgeting, effective and efficient operations management, equipment utilization, safety and environmental compliance as well as personnel management.
NewResidential Construction Project Manager Pop-Up TalentResidential Construction Project ManagerVentura, CA$90,000–$120,000 / yearWorking closely with the design and construction teams, the Project Manager will perform the following tasks: Assemble scopes of work, direct value engineering exercises, and develop estimates and proposals. If you feel you are ready for the next step in your career, feel overlooked, or are just looking for someone to give you a chance, then this might just be what you are looking for.
NewRESTAURANT MANAGER Stonefire Grill Restaurant ManRESTAURANT MANAGERVentura, CA$25–$27 / hourEqually important and connected is the partnership with the General Manager (GM), Assistant General Manager (AGM), and Executive Kitchen Manager (EKM) in overseeing the planning, organizing, training, and development of each individual manager and team member, as well as the shared achievement of stated objectives in finance, safety, quality and the cultural environment of the restaurant. In partnership with the General Manager and Assistant General Manager, manages restaurant team consisting of Heart of the House and FOH Team Members, and Caterers.
NewProject Manager - Residential Construction Bevyhouse LLCProject Manager - Residential ConstructionVentura, CAWorking closely with the design and construction teams, the Project Manager will perform the following tasks: Assemble scopes of work, direct value engineering exercises, and develop estimates and proposals. If you feel you are ready for the next step in your career, feel over looked or are just looking for someone to give you a chance, then this might just be what you are looking for.
Development Project Manager - Multifamily Michael Page USADevelopment Project Manager - MultifamilyTarzana, CA$170,000–$200,000 / yearFull timeReporting to the VP of Development, the Project Manager will be responsible for the following: Manage the entitlement process with the City of Los Angeles, including coordination with LADBS, Planning Department, and the Warner Center Specific Plan review process. Specializing in ground up multifamily, mixed-use, industrial, and hospitality projects, the team has consistently delivered top products across their 20 year history.
Sr Quality Engineer (New Product Development) MiniMedSr Quality Engineer (New Product Development)Northridge, CaliforniaWe are seeking a highly motivated and detail-oriented S enior Quality Engineer to lead and implement Design Quality Engineering activities for diabetes management products, including insulin pumps, continuous glucose monitoring (CGM) systems, and closed-loop / automated insulin delivery systems. If you are applying to perform work for MiniMed in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which MiniMed reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Sr Quality Engineer (New Product Development) MinimedSr Quality Engineer (New Product Development)Northridge, CA$87,000–$149,000 / yearWe are seeking a highly motivated and detail-oriented Senior Quality Engineer to lead and implement Design Quality Engineering activities for diabetes management products, including insulin pumps, continuous glucose monitoring (CGM) systems, and closed-loop / automated insulin delivery systems. If you are applying to perform work for MiniMed in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which MiniMed reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Sr. Product Development Engineer Freudenberg GroupSr. Product Development EngineerCarpinteria, CATranslate customer requirements, user needs and/or other inputs into clear design requirements, specifications, and design input documentation (as applicable); participate in and lead risk management activities, design/project reviews, and verification testing to ensure product safety and efficacy; apply engineering analysis, design principles, and risk management tools to drive sound design decisions. Partner with customers/clinicians, marketing, regulatory, quality, NPI/manufacturing, and external experts to develop novel medical devices, assess new technologies/processes, and ensure clinical relevance and manufacturability of designs.
Engineer, Drug Product Development, Process Design & Experimentation - Hybrid (JP14756) 3 Key ConsultingEngineer, Drug Product Development, Process Design & Experimentation - Hybrid (JP14756)Thousand Oaks, CaliforniaProvide ongoing support to clinical and commercial fill/finish manufacturing operations through troubleshooting, root cause analysis, and product impact assessments for non-conformance investigations and process changes/improvements. Experience in development/characterization of aseptic fill/finish unit operations (freeze/thaw, mixing, sterile filtration, filling, stoppering, visual inspection, etc.) to define critical process parameters.
Sr. Product Development Engineer FreudenbergSr. Product Development EngineerCarpinteria, CaliforniaTranslate customer requirements, user needs and/or other inputs into clear design requirements, specifications, and design input documentation (as applicable); participate in and lead risk management activities, design/project reviews, and verification testing to ensure product safety and efficacy; apply engineering analysis, design principles, and risk management tools to drive sound design decisions. Partner with customers/clinicians, marketing, regulatory, quality, NPI/manufacturing, and external experts to develop novel medical devices, assess new technologies/processes, and ensure clinical relevance and manufacturability of designs.
Engineer, Drug Product Process Development and Tech Transfer Project Support - (JP15165) 3 Key ConsultingEngineer, Drug Product Process Development and Tech Transfer Project Support - (JP15165)Thousand Oaks, CaliforniaThe ideal candidate will have expertise in laboratory testing, drug product fill finish processing, holistic drug product process knowledge, technical transfer, and drug product manufacturing. Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience.
Packaging Development Engineer – Secondary & Tertiary Packaging Innovation (Biologics / Combination Products / GMP) (JP15071N) 3 Key ConsultingPackaging Development Engineer – Secondary & Tertiary Packaging Innovation (Biologics / Combination Products / GMP) (JP15071N)Thousand Oaks, CaliforniaKey responsibilities include designing and improving cartons, labels, inserts, and distribution packaging; maintaining component specifications; leading engineering studies; evaluating new materials and packaging technologies; supporting supplier qualification activities; and ensuring packaging systems meet performance, traceability, and global compliance requirements. The successful candidate will work cross-functionally with Operations, Quality, Supply Chain, Regulatory, Device Development, and external suppliers to drive packaging innovation, improve manufacturability, ensure regulatory compliance, and support product launches, technology transfers, and supply continuity.
Drug Product Visual Inspection Process Development Engineer (Aseptic Fill/Finish) - (JP15200) 3 Key ConsultingDrug Product Visual Inspection Process Development Engineer (Aseptic Fill/Finish) - (JP15200)Thousand Oaks, CaliforniaThe candidate will establish the experimental design, develop and implement protocols, obtain reproducible and reliable results, analyze data and communicate results to cross functional groups. Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience.
Engineer, Drug Product Process Development & Technology Transfer - (JP15153) 3 Key ConsultingEngineer, Drug Product Process Development & Technology Transfer - (JP15153)Thousand Oaks, CaliforniaAs a member of the process development team, the candidate will be focused on supporting senior staff to develop and characterize drug product technologies and manufacturing capabilities, as well as assist in the process validation and technology transfer of multiple products to the aseptic fill finish manufacturing plants and which includes various production lines. The candidate will be primarily responsible for executing characterization studies and other experiments at the lab scale and production scale to generate technical data packages using complex technology, while organizing data and analyzing results under supervision of senior staff.
Engineer, Drug Product Process Development and Tech Transfer Project Support - (JP15004) 3 Key ConsultingEngineer, Drug Product Process Development and Tech Transfer Project Support - (JP15004)Thousand Oaks, CaliforniaAs a member of the process development team, the candidate will be focused on supporting senior staff to develop and characterize drug product technologies and manufacturing capabilities, as well as assist in the process validation and technology transfer of multiple client products to the aseptic fill finish manufacturing plants within their Thousand Oaks facilities and which includes various production lines. The candidate will be primarily responsible for executing characterization studies and other experiments at the lab scale and production scale to generate technical data packages using complex technology, while organizing data and analyzing results under supervision of senior staff.
Process Development Senior Scientist - Drug Product Technologies Amgen Inc.Process Development Senior Scientist - Drug Product TechnologiesThousand Oaks, CAIn addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. The role involves designing and developing liquid and lyophilized formulations; evaluating critical quality attributes (CQAs); establishing robust, scalable fill/finish processes for complex biologic drug products; and authoring and supporting high quality regulatory submissions.
Process Development Senior Scientist - Pre-Pivotal Drug Product Technologies AmgenProcess Development Senior Scientist - Pre-Pivotal Drug Product TechnologiesThousand Oaks, CaliforniaIn addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. The role involves designing and developing liquid and lyophilized formulations; evaluating critical quality attributes (CQAs); establishing robust, scalable fill/finish processes for complex biologic drug products; and authoring and supporting high quality regulatory submissions.