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  1. Clinical Research Medical Director, Bone at Amgen

    Two (2) + years of clinical research experience and/or basic science research. Five (5) + years of clinical research experience and/or basic science research...

  2. Clinical Research Medical Director, Neuroscience at Amgen

    Five (5) or more years of clinical research experience and/or basic science research combined with clinical teaching and patient care activities....

  3. Senior Counsel - Corporate Transactions at Amgen

    Significant M&A and/or licensing transactions experience, with a strong preference for biotech or pharmaceutical transactions experience....

  4. Dir Clinical Trial Patient Engagement Technology at Amgen

    11+ years work experience in product development, including 8 years of biopharmaceutical clinical product development (includes clinical research and clinical...

  5. Training & Development Mgr, Hematology/Oncology at Amgen

    4+ years of biotech or pharmaceutical hematology/oncology selling experience. Responsible for execution, coordination and adaptation of field sales training for...

    Ads
    1. Business Development Manager 340.16TS

      :: If you meet the qualifications listed below and would like more information contact Tamra at 815-756-1221 Attach resume when responding to this posting :: The Business Development Manager will be responsible for identifying and building new areas of business; creative and critical thinking that will expand product offerings within new, innovative categories of the food industry. ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    1. Process Technician - Bakery Lab at Snyder's-Lance

      R & D/Quality. Monitoring of product in manufacturing including color, moisture, PH, weight, size etc. (State overall purpose of the job in 2-3 sentences)....

    1. Senior Regulatory Affairs Specialist [16-00896]

      We are seeking a Senior Regulatory Affairs Specialist who will develop regulatory submissions and assessments (in compliance with applicable regulations and standards) to ensure timely global commercialization of products. ESSENTIAL DUTIES AND RESPONSIBILITIES With moderate supervision, responsible for the following Regulatory activities: 1. Develop and implement regulatory strategies and ...

    1. CNC/Manual Lathe Operator at Edgewater Automation

      Director of Manufacturing. We have experience in a broad range of industries including energy, life sciences, transportation, consumer goods, and electrical....

    1. Instrumentation Technician III - 1650012934

      DescriptionAt Agensys, we're changing tomorrow by moving oncology forward. We've developed a pipeline of novel therapeutic fully human monoclonal antibodies (MAbs) to treat solid tumors based on our own proprietary targets. We have discovered and validated a portfolio of clinically relevant targets in 14 different cancer types. Our pipeline includes therapeutic MAbs to multiple cancer ...

    1. GE Power Technical EID (Intern/Co-Op) at GE Power

      Support manufacturing engineering projects involving manufacturing process improvements and product cost reduction....

    1. Product Development Manager 233.16KO

      :: If you meet the qualifications listed below and would like more information contact Kristine at 815-756-1221 Attach resume when responding to this posting :: The Product Development Manager will be responsible for successfully commercializing new ingredients of a complex nature for use in recipes. Qualifications: -BS in food science; advanced degree preferred -5+ years of manufacturing or ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    1. Manufacturing/Supply Chain EID Intern at GE Energy Connections

      EID Responsibilities Manufacturing:. Strong commitment to career in manufacturing. Environmental engineering, chemical engineering, material science engineering...

    1. BioPharma Computer Systems Validation Project Manager

      This is an exciting international Expatriate Project Management opportunity responsible for leading a broad set of Computer Systems Validation (CSV) activities within a state of the art startup commercial biologics manufacturing facility. This is a unique opportunity within an industry leading large scale Global Contract Manufacturing Organization (CMO) backed by a major multinational ...

    1. Building Management Engineer II at Pacira Pharmaceuticals

      Minimum of 3 years of Pharmaceutical Manufacturing Experience. BS Degree in Computer Science/ Electrical/ Mechanical/ Chemical Engineering or equivalent...

    1. Validation Engineers & Validation Specialists

      Compli, LLC is a Validation and Regulatory Compliance Contract Services Provider dedicated to providing the Pharmaceutical, Biotechnology, and Medical Device Industries with high quality consulting services. We are currently looking for individuals to support our clients and projects throughout the United States.We are interested in Validation Engineers/Specialists with experience in ...

    1. Temp Lab Technician 1 at Hologic

      SUMMARY This position will be required to support two areas that support our RMA/reverse logistics processes on instrumentation and spare parts. Will be

    1. Plant Quality Assurance Manager 387.16AM

      :: If you meet the qualifications listed below and would like more information contact Amanda at 815-756-1221 Attach resume when responding to this posting :: The Plant Quality Assurance Manager will be responsible for managing all resources related to quality with in manufacturing plant and supporting facilities. Qualifications: -BS in food science or biological science -5+ years of quality ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    1. Director Product Development/Environmental Care at Dussick Management Associates

      Translate customer marketing goals into technical specifications to assure a focused R & D effort. Master’s degree in science required....

    1. QA Packaging Associate

      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: QA Packaging AssociateJob ID: 2476Industry: Biotech/PharmaceuticalLocation: Thousand Oaks, CADuration: 18 Month ContractPay Rate Range: Depends on Experience (W2, no benefits ...

    1. Product Mgmt/Strategy Director-ProdDev at Oracle

      Manage a team that acts as the central resource and driving force for the design, process, manufacturing, test, quality and marketing of product(s) as they move...

    1. Principal Associate - 1550005200-01

      Description:At Agensys, we're changing tomorrow by moving oncology forward. We've developed a pipeline of novel therapeutic fully human monoclonal antibodies (MAbs) to treat solid tumors based on our own proprietary targets. We have discovered and validated a portfolio of clinically relevant targets in 14 different cancer types. Our pipeline includes therapeutic MAbs to multiple cancer ...

    1. Downstream Scientist I to IV (Operator), Clinical Manufacturing at Oncobiologics, Inc.

      Life Sciences or equivalent. The Downstream Scientist (Operator) I to IV, Manufacturing, will execute downstream manufacturing operations as Oncobiologics...

    1. Instrumentation Technician III - 1650012934

      Description:At Agensys, we're changing tomorrow by moving oncology forward. We've developed a pipeline of novel therapeutic fully human monoclonal antibodies (MAbs) to treat solid tumors based on our own proprietary targets. We have discovered and validated a portfolio of clinically relevant targets in 14 different cancer types. Our pipeline includes therapeutic MAbs to multiple cancer ...

    1. Optical Thin Film Coating Expert at Qualitec

      Ideal) of experience working in a laboratory / manufacturing industry. Advanced degree in Physics, Chemistry, Materials Science, or Engineering with 6 to 12 yrs...

    1. Sr. Validation Specialist/ Sr. Engineer

      Azzur Group CA is seeking a Sr. Validation Specialist/Sr Engineer. In this role, you will be responsible for performing equipment, cleaning, and process and/or facilities validation. Essential Duties and Responsibilities· Performs/ executes/ validates (IQ, OQ, PQ) for Equipment, Cleaning and Facilities Validation and Computer System Validation (CSV).· Writes, and executes protocols, reviews ...

    2. Senior Quality Specialist 14.16MR

      :: If you meet the qualifications listed below and would like more information contact Mary at 815-756-1221. Attach resume when responding to this posting :: The Senior Quality Specialist will be responsible for executing the strategies as established to ensure the production of the highest quality products in the safest and most efficient manner. 50% travel Qualifications: -BS/MS in food ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    3. Senior Regulatory Affairs Specialist - Contract

      This is a full-time, contract position for approximately 6 months.POSITION SUMMARY:  Working with minimal supervision, manage complex projects/products, including responsibility for the content, assembly, pre-final review, and filing of major medical device applications (e.g., IDEs, PMAs, 510(k)s) submitted to the FDA and foreign regulatory agencies.  SPECIFIC DUTIES AND RESPONSIBILITIES: ...

    4. 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, ...

    5. IVD Material Planner

      To manage and report on materials, supply and warehouse operations of DxTerity products. This position has a to ensure products are manufactured in compliance with FDA-mandated design controls and ISO 13485 requirements. To oversee Inventory Management, and Supply using materials planning, inventory maintenance, storage, and shipping/receiving methods and best practices. To ensure the timely ...

    6. Sr. Associate Regulatory Affairs (CMC)

      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: Sr. Associate Regulatory AffairsJob ID: 2462Industry: Biotech/PharmaceuticalLocation: Thousand Oaks, CADuration: 9 Month ContractPay Rate Range: Depends on Experience (W2, no ...

    7. Project Manager (Part Time, 20hrs/week)

      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: Project Manager (Part-Time)Job ID: 2457Industry: Biotech/PharmaceuticalLocation: Thousand Oaks, CADuration: 7 Month ContractPay Rate Range: Depends on Experience (W2, no ...

    8. 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 ...

    9. 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, ...

    10. Research Scientist - Surface Chemist / Research & Development PhD

      Senior Research Scientist – Surface ChemistMajor Fortune 500 Company located on the West Coast, Headquartered in Los Angeles, California is seeking a Senior Research Scientist. Must have a Ph.D in Organic Chemistry and a minimum of 2 to 4 years of Industry experience in surface science, surface modification and troubleshooting. You will be responsible for leading and R&D team to develop, ...

      1. Process/Manufacturing Engineer at Mission Critical Composites

        Bachelor of Science in Engineering (from a United States University) with minimum of 5 years' manufacturing experience in aerospace / defense or commercial...

      2. QC Supervisor - 2nd shift at Torn & Glasser

        Manufacturing Quality Control:. Bachelor level degree preferred or equivalent in science related field. Minimum of 3 - 5 years experience working in a food...

      3. Help Wanted at It’s Boba Time

        Now hiring at 1001 South Alvarado Street, Los...

      4. Machinist III - 8/2016 at Iscar Metals, Inc.

        Abil i t y to r ea d a nd in t e r p r e t produ c t i on d r a win g s. B a sic c ompu t e r skil l s. Diplo m a c y a nd a bi l i t y to fun c t i on a s a m...

      5. Quality Assurance Supervisor at DCI Donor Services

        Bachelor’s degree in science or allied healthcare field. Investigate quality and manufacturing roadblocks to ensure timely release of tissue....