Quality Assurance Engineer to join leading Medical Biotech Company in Irvine, CA. Quality Assurance Engineer near ... Description Quality Assurance Engineer to join leading Medical Biotech Company in Irvine, CA. Required Skills Quality Engineer, biotech, pharmaceutical, SIX Sigma Green Belt, quality control, regulatory ... Eskovitz Date Updated 11/30/2008 Skills Required Quality Engineer, biotech, pharmaceutical, SIX Sigma Green Belt, quality control, regulatory compliance, cGMP/MDD/ISO, Statistics expertise Job Description We have an outstanding career opportunity for a Quality ...

Quality Assurance Engineer to join leading Medical Biotech Company in Irvine, CA. Quality Assurance Engineer near ... Description Quality Assurance Engineer to join leading Medical Biotech Company in Irvine, CA. Required Skills Quality Engineer, biotech, pharmaceutical, SIX Sigma Green Belt, quality control, regulatory ... Eskovitz Date Updated 11/28/2008 Skills Required Quality Engineer, biotech, pharmaceutical, SIX Sigma Green Belt, quality control, regulatory compliance, cGMP/MDD/ISO, Statistics expertise Job Description We have an outstanding career opportunity for a Quality ...

Quality Assurance Engineer to join leading Medical Biotech Company in Irvine, CA. Quality Assurance Engineer near ... Description Quality Assurance Engineer to join leading Medical Biotech Company in Irvine, CA. Required Skills Quality Engineer, biotech, pharmaceutical, SIX Sigma Green Belt, quality control, regulatory ... Eskovitz Date Updated 11/27/2008 Skills Required Quality Engineer, biotech, pharmaceutical, SIX Sigma Green Belt, quality control, regulatory compliance, cGMP/MDD/ISO, Statistics expertise Job Description We have an outstanding career opportunity for a Quality ...

... Description Quality Assurance Engineer to join leading Medical Biotech Company in Irvine, CA. Required Skills Quality Engineer, biotech, pharmaceutical, SIX Sigma Green Belt, quality control, regulatory ... Eskovitz Date Updated 11/20/2008 Skills Required Quality Engineer, biotech, pharmaceutical, SIX Sigma Green Belt, quality control, regulatory ... for a Quality Assurance Engineer with pharmaceutical or biotech manufacturing experience to join a ...

Job Title: Sterile Filling Operations Supervisor - Pharmaceutical, 3rd Shift Location: Confidential - Chicago area, Illinois Job Description: We seek a talented, degreed professional with five years experience in supervising an aseptic filling operation in a pharmaceutical environment which is regulated by the US FDA to assume a key leadership role at our client company's IL facility. You will manage a third-shift team of Operators to achieve output, cost and quality results and ensure substantial compliance with cGMP standards. The ideal candidate must have experience in a sterile FDA regulated manufacturing pharmaceutical/biotech facility. Job Duties: You will be responsible for filling, ...

BIOTECH: ASSOC. DIR MFG, CELL CULTURE We have over 100 active position listed on our website. Please visit http://protechpharma.co Assoc. Dir Manufacturing, Cell Culture LOCATION: NJ-Central RESPONSIBILITIES: This position is responsible for providing effective leadership to the cell culture manufacturing operations for the commercial production of monoclonal antibody products. This position reports to the Senior Director of commercial manufacturing and interacts with engineering, maintenance, validation, quality assurance, quality control, clinical development and logistics departments. As needed, further interaction will be required with material vendors and commercial partners. Knowledge of cell culture operations and support systems, along with spreadsheets and databases ...

MANUFACTURING MANUFACTURING TECHNICIAN A fast growing biotech company located in Research Park is looking for ... relevant work experience. We are a fast growing biotech company located in Research Park near the U of U. We offer competitive salaries, benefits and a 401k in a stimulating work environment. Please send your resume to: HR, Idaho Technology, 390 Wakara Way, Salt Lake City, UT 84108 or by email: hr@idahotech.com To learn more visit us at www.idahotech.com. We are an EOE employer ...

DIRECT Quality Inspector CAM biotech co seeks QC Inspector. Duties incl inspection of raw materials, in-process and final inspection. Knowledge of calipers and basic QC tools req'd. Fax/ email resume 805- 388-7313/ kvarner@ medicalpackaging.comWebID: 178084 Posting provided by: ...

... include testing and quality process procedures on?pharmaceutical and biotech client product. Candidate will follow and carry out FDA and cGMP related internal audits and inspections as well as documentation control, SOP review and creation of related reports, and overall assistance to the QA Manager.??Candidate must possess a minimum of a?Bachelors degree in Biology or related scientific field, familiarity with FDA and cGMP standards and procedures, strong attention to detail with excellent written and oral communication skill. This position is a ...

Quality Assurance Management role open in New Hampshire QA Mgr in NH Medical Device/Biotech or Pharmaceutical Background will be considered Develops, implements, and coordinates product assurance program to prevent or eliminate defects in new or existing products by performing the outlined duties personally or through subordinate positions. Responsible for the regulatory affairs of the organization. Personnel Supervised: Quality Technicians Senior Quality Technicians Quality Engineers Quality Supervisor Experience: (Required and Desired) Prior Quality Assurance management experience is required, including FDA, GMP, ISO, regulatory, facility, statistics and analysis, SPC, clean room microbiology and training programs is required. Prior medical manufacturing experience is desired. ...

... II Job Title Manufacturing Technician II Division Stryker Biotech Location (Country - State) United States - Massachusetts City or Sales Region Hopkinton Business Function Manufacturing/Operations Shift 1st Education and/or Special Training See Qualifications Job Description This position has primary responsibility to support in the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with GMP, QS, ISO regulations and guidelines.? Product manufacturing ? Completion of routine documentation associated with the manufacture of product ? Support activities in-process and product development when instructed by supervisor ? Incorporate pre-planned process improvements/cost ...