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document control in Los Angeles

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  1. Sr. Quality Engineer Medical Device at iRhythm Technologies, Inc.

    Plans, develops, implements, and maintains the document change control system. Bachelor’s Degree in an applied science or engineering field....

  2. IT Release Management Analyst at L.A. Care Health Plan

    Bachelor's of Science in Computer Science, Information Systems and Configuration Management, Computer Engineering or related field;...

  3. Full Stack Engineer / Team Leader at Anivive

    Understanding of Agile software development, GIT workflow and version control (Jira/Perforce/SVN/Bugzilla/GIT/GitFlow)....

  4. Clinical App & Analytical Svcs Mgr at Amgen

    BA/BS/BSc in the sciences or RN. 5 years work experience in life sciences or medically related field, including 4 years of biopharmaceutical clinical product...

  5. Business Unit Quality Management Technologist at Mars, Incorporated

    NA Business Unit Document Control Program Owner including maintaining documents that are up to date and are aligned with Corporate and Segment Q&FS requirements...

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    1. Manager, Regulatory Affairs

      POSITION SUMMARY:   The position is responsible for diverse regulatory functions, including but not exclusive to the development of Medical Device submissions and the implementation of Regulatory Compliance.ESSENTIAL DUTIES AND RESPONSIBILITIES:   ·         Prepares submissions and applications to US and OUS regulatory agencies to request approval to conduct clinical trials, to request ...

    1. Senior Linux Administrator at Digital Domain 3.0 Inc

      Familiarity with version control systems. Document system installations, configurations, policies and procedures....

    1. Director Regulatory Affairs - Medical Device

      Overview: As part of the leadership team the Director of Regulatory Affairs will play a key role in developing and implementing global Regulatory strategies for Class II/III medical devices This individual will be the Regulatory subject matter expert for all applicable medical devices. S/he will need to identify, assess and communicate regulatory development and submission strategies, ...

    1. Assistant Manager at Hillstone Restaurant Group

      Hillstone Restaurant Group is a privately-held collection of upscale restaurants with 45+ locations in major cities across the country. Some of our more well

    1. Specimen Accessioner

      Duties: Prepares laboratory specimens for designated departments/locations prior to laboratory analysis and testing. Unpacks specimens from branches or ports and routes specimens by type to various staging areas. Prepares all specimens received for testing in designated laboratory departments or locations such as staging of specimens, centrifuge, separate serum, and blood smears. May perform ...

    1. In Mkt OTE Proj Coord, AL/FL at FL

      Lea rn in g an d development solution sets based on a broad spectrum of potential interventions. M easu re s pe r formance trends and develops new programs or...

    1. Validation Engineer - Consultant - Los Angeles Metro areas

      Responsibilities:A Validation Engineer at ProPharma Group will work with our Clients and be responsible for preparing and executing validation documents.   Working knowledge of the principles of validation as associated with performance of work for the Life Sciences industries.  Demonstrate an understanding of GMP.   Individuals must represent the company and division at client sites and ...

    1. Senior Data Scientist at Loot Crate

      2+ years of experience with R and/or Python(pandas/numpy/scipy). The Data Scientist will be an integral part of the Loot Crate data team and will be responsible...

    1. Junior GxP Document Management Role

      PSC Biotech is one of the leading biotechnology consulting firms in the pharmaceutical and biotech industry. We are currently looking for a junior professional for our client in Seattle, WA. Requirement: Bachelor's degree in biomedical, chemical, mechanical engineering or any related fieldCandidate must have minimum experience in GxP environment (GMP, GLP, GCP)Worked in a GMP document control ...

    1. RN Clinical Staff ED FT Days at Martin Luther King, Jr. Community Hospital

      Assists patient/family to maximize sense of control and actively participate in his/her recovery. Evaluates the effectiveness of nursing interventions and...

    1. Mgr-PharmD ONLY, work from home-anywhere in US

      Important NoteU.S. Doctor of Pharmacy (Pharm.D.) is Required.Your submission is not considered complete until CV/Resume and Application is submitted to [email removed]. Submission instructions and Application are located on the Join Me tab at www.wesleyenterprise.net.This document describes the position. It is not an employment contract. Our company reserves the right to modify job duties or ...

    1. RN Clinical Staff Telemetry FT Nights at Martin Luther King, Jr. Community Hospital

      Assists patient/family to maximize sense of control and actively participate in his/her recovery. Evaluates the effectiveness of nursing interventions and...

    1. Document Control Technician

       The Document Control Technician is responsible for processing and maintaining all controlled documents in regulatory affairs. Responsibilities include creating, editing, indexing, tracking, and storage of documents as cGMP guidelines.Responsibilities: Issuance of approved SOP’s and maintain a log of all SOP’s on the floor.File and maintain SOP's, Master and executed batch records, packaging, ...

    1. RN Clinical Staff ICU FT Nights at Martin Luther King, Jr. Community Hospital

      Assists patient/family to maximize sense of control and actively participate in his/her recovery. Evaluates the effectiveness of nursing interventions and...

    1. Director Regulatory Affairs

      Overview: As part of the leadership team the Director of Regulatory Affairs will play a key role in developing and implementing global Regulatory strategies for Class II/III medical devices This individual will be the Regulatory subject matter expert for all applicable medical devices. S/he will need to identify, assess and communicate regulatory development and submission strategies, ...

    1. RN Clinical Staff ED FT Nights at Martin Luther King, Jr. Community Hospital

      Assists patient/family to maximize sense of control and actively participate in his/her recovery. Evaluates the effectiveness of nursing interventions and...

    1. PRODUCT CLAIMS SUBSTANTIATION ASSOCIATE

      A profitable and expanding, quality-minded vitamin company located in Los Angeles, California is searching for an excellent Product Claims Substantiation Associate.TITLE: PRODUCT CLAIMS SUBSTANTIATION ASSOCIATEDEPARTMENT: Technical SupportREPORTS TO: Directors & UpSalary/Wage: $60,000 - $75,000 per Annum, DOEE Job Description: Provides technical support to scientific validation of product ...

    1. EXECUTIVE CATERING CHEF KITCHEN MANAGER at SUMMIT EVENT CATERING

      RECIPE CREATION, INNOVATION WITH REGULAR R AND D DAYS. EXECUTIVE CATERING CHEF (KITCHEN MANAGER)*....

    1. Principal Scientist - Food Science - Protein Powders - Snack Bars

      The Principal Scientist serves as a technical leader and source of expert knowledge in advanced principles, concepts and theory related to product and/or process development. The position accountabilities include identifying, documenting and validating the appropriate ingredients, formulations and unit processes that meet product standards and requirements, including product costs, quality, ...

    1. Assistant Professor - Nursing at West Coast University

      Member as set forth in regulatory documents. Graduates from the West Coast University Master of Science in....

    1. Clinical Affairs Manager

       Job DescriptionThe Clinical Affairs position will assist the Clinical Affairs Director in planning, coordinating and completing studies. The candidate needs to have excellent communication and presentation skills, together with the ability to organize and motivate others. The candidate must demonstrate enthusiasm, innovation and leadership when faced with challenges and will provide ...

    2. Laboratory Technician

      Job Title: Associate Mfg – Cell Culture (Laboratory Technician)Pay: up to $18.50/hrLocation: Thousand Oaks, CA 91320Length: 18 month contract with possible extension Job Description:· This Cell Culture Manufacturing Associate position will support the re-commissioning and start-up of commercial cell culture drug substance intermediate manufacturing operations in Thousand Oaks, CA. The Sr. ...

    3. R&D Associate

      A profitable and expanding, quality-minded vitamin company located in Los Angeles, California is searching for an excellent R&D Associate.JOB TITLE: R&D AssociateDepartment: R&DReports to: EVPSalary Range: $50,000-$70,000 per yearPosition Description:This position provides support to Research & Development Department staff, including EVP, Directors, QA/QC, Marketing, Production and ...

    4. Sr Associate, Software Labeling Lead (Regulatory)

      Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis. Title: Senior Associate Software Labeling LeadJob ID: 2419Industry: Biotech/PharmaceuticalLocation: Thousand Oaks, CADuration: 11 Month ContractPay Rate Range: Depends on Experience ...

    5. Technical Supervisor – LC/MS

      Copy the following address into your browser to apply: https://gethired.com/job/technical-supervisor-lc-ms?rcid=ebay We are looking for someone that is extremely proficient in using LC/MS in a clinical setting. This person will be responsible for ensuring the accuracy of the LC/MS/MS assays used by InSource. The role requires direct involvement with the daily review and quantitation of data. ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    6. Clinical Lab Scientist (CLS) – LC/MS

      Copy the following address into your browser to apply: https://gethired.com/job/clinical-lab-scientist-cls-lc-ms?rcid=ebay Testing Personnel are responsible for running and quantitation of clinical samples using LC/MS/MS. Role Specific Responsibilities  Must have experience with Liquid Chromatography/Mass Spectrometry (LC/MS). Experience on SCIEX 4000 or 5000 systems is preferred, but not ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    7. Inventory Control Shipping Technician-6617

      Inventory Control Shipping Technician- Simply BiotechOVERVIEWImmediate opening for a Inventory Control Shipping Technician in Torrance, CA who possesses:HS diploma or equivalent industrial experience.Basic understanding of Chemistry.Strong knowledge of domestic (DOT)and international (AITA) shipping procedures, including customs regulations and paperwork (i.e. NAFTA forms, Commercial Invoice, ...

    8. Purchasing

      Dietary supplement manufacture looking to hire a purchasing agent with at least 2 years experience in a manufacturing environment. Prior work in a pharmaceutical or dietary supplements is preferred. Also basic knowledge with QuickBooks and how to create a purchase order, sales order, and invoice is a plus.Purchasing Agent Job Duties:·         Verifies purchase requisitions by comparing items ...

    9. Reliability Engineer

      Azzur of CA is looking for a Reliability Engineer with Quality and Change Control experience to support the reliability group in document change control initiation, tracking and completion. Experience with BPLM and JDE is required. TrackWise experience is a plus.  Essential Duties and Responsibilities· Perform gap analysis through BPLM and JDE systems.· Support the reliability group in the ...

    10. R&D Associate

      A profitable and expanding, quality-minded vitamin company located in Los Angeles, California is searching for an excellent R&D Associate.JOB TITLE: R&D AssociateDepartment: R&DReports to: EVPSalary Range: $50,000-$70,000 per yearPosition Description:This position provides support to Research & Development Department staff, including EVP, Directors, QA/QC, Marketing, Production and ...

      1. Study Management - Sr. Manager at Amgen

        Coordinate the development, and contribute to the writing and review of study related documents, including Study Concept Document and Protocol....

      2. Biostatistics Sr Mgr at Amgen

        Fluency in R and SAS. 4+ years as a statistician in a pharmaceutical or biotech industry with clinical trial/regulatory interaction (including NDA filing)...

      3. Senior Technical Support Scientist - ForteBio Division (Label Free Instrumentation) at Pall

        Degree in Chemistry, Biology - or related physical sciences. Pall Life Sciences provides cutting-edge products and services to meet the demanding needs of...

      4. Senior Data Scientist at Microsoft

        SAS, SPSS, R, Mahout. Java, Python, R, F#, C#. The Microsoft Data Insights Domain is looking for Sr....

      5. Appliance Repair Technician at Miele, Inc.

        Summary Travel to customer location to diagnose, troubleshoot and repair Miele appliances utilizing factory training, service manuals and computerized tools