Biotech Quality Assurance Specialist Jobs

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Clinical Solutions Group Bernardsville, NJ
Quality Assurance Specialist: 1) Responsible for entering Customer Complaint information into the tracking systems (EtQ, Excel, etc.). -Reviews received documentation and works with the Customer Care and Drug Safety departments to resolve documentation issues regarding source complaint documents. -Performs data entry of all received product quality complaints into the electronic complaint syste...
Analytical and Process (A&P) Calibrations serves the biotechnology, microchip and other manufacturing industries in the San Francisco Bay Area and beyond. Since its founding, we have applied more than 25 years of experience in the calibration services industry, combined with our experience as end users of calibration equipment in the biotechnology industry, to our professional, high quality calibr...
Job Title: QA Specialist I: QC Oversight Location: Holly Springs, NC Duties: Job Purpose: Personnel is responsible for quality oversight of commissioning and qualification of laboratory equipment and Quality Control areas. Role will support QC areas in Building Alarm System quality oversight by reviewing daily alarms, and assessments including deviation review and approval in the Trackwise sys...
Responsibilities: Provides backup support for QA for the review and release of manufacturing Batch Records. Works on QA related projects such as training binder archiving, preparing documents for offsite storage, matrix project and supplier retrospective evaluation. Assist training coordinator with maintaining the department training matrix and training completion activities. Requirements: An...
Job Description The Sr. GMP QA Specialist develops and maintains quality systems to meet US and EU requirements, including, but not limited to deviations, investigations, change controls, batch disposition, external and internal auditing, to support the Development Quality Organization and ensuring compliance to Good Manufacturing Practice (GMP). Provide support for review and approval of COAs, C...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply Regulatory Affairs Carson, CA; El Segundo, CA Full-Time $50,000 - $90,000 Apply Apply Regulatory Affairs Carson, CA; El Segundo, CA Full-Time $50,000 - $90,000 Apply Job Details If you are a Regulatory Affairs and Compliance Associate with 3+ years of submitting drug master files, please read on...
Auto req ID: 2604BR Job Posting Title: QA Raw Materials Supplier Specialist Person Type: Regular Posting Category: QA, QC & Quality Auditing Additional Posting Category: Industrial Operations & Product Supply Location: Rensselaer Job Summary and Essential Functions: Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discov...
Auto req ID: 1746BR Job Posting Title: QA Material Supplier Specialist Person Type: Regular Posting Category: QA, QC & Quality Auditing Additional Posting Category: Facilities & Maintenance Location: Rensselaer Job Summary and Essential Functions: Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, deve...
Oct 16, 2014 CSC has an immediate position for a Computer Validation Specialist within the DOC systems group. This position is located in Frederick, Maryland. Essential Job Functions Ensure IT infrastructure, hardware and software systems purchased by DVC for the regulated network are installed, perform and operate according to specifications and user requirements. Lead qualification and valida...
HFluitt & Associates San Jose, CA
Full-time United States - California - Santa Clara The Compensation Base Salary - Salary Confidential per Client's Request Benefits - Full Relocation Assistance Available - No Commission Compensation - No Bonus Eligible - Yes Overtime Eligible - No Interview Travel Reimbursed – No Local Candidates Only-Or within commuting distance Detailed Description As an individual contributor, the ...
Description CSC has an immediate position for a Computer Validation Specialist within the DOC Systems group. This position is located in Frederick, Maryland. Essential Job Functions Ensure IT infrastructure, hardware and software systems purchased by DVC for the regulated network are installed, perform and operate according to specifications and user requirements. Lead qualification and valida...
Clinical Solutions Group Durham, NC
The Site Recruitment Specialist will perform, manage and coordinate activities associated with identification of sites for projects or programs. RESPONSIBILITIES • Take independent responsibility for assigned site identification projects. • Assists Site Recruitment lead on projects with increased protocol complexity, site numbers and/or customer SOPs or processes. • Utilizes historic site perf...
Cambridge Major Laboratories, Inc. is a leading provider of complex chemistry services that includes development, characterization, and manufacturing of active pharmaceutical ingredients and pharmaceutical intermediates. We have experienced significant growth since our founding in 1999, and have continued to attract the most highly skilled professionals in the industry. QUALITY ASSURANCE SPECIALI...
Company IPS-Integrated Project Services Branch Portsmouth NH US Position: QA Specialist Location: Portsmouth, NH engineering, construction, commissioning and qualification of complex pharmaceutical and biotech research and manufacturing facilities. With technical expertise… Position Responsibilities: IPS has an immediate need for a QA Specialist with our client in Portsmouth, NH. The QA S...
America's Job Exchange
Description Expertise Quality Assurance Education High School/GED Job Type Full-time Location United States - Indiana - Indianapolis Job Level Experienced Job Description: Posting date: March 31, 2014 COMPANY INFORMATION THE BIOPHARMA SERVICES DIVISION (BSD) OF THERMO FISHER SCIENTIFIC is a cohesive group of businesses that play a critical/integral part in delivering life saving and life-enhanci...
Senior QA Specialist Requisition ID -00432403 The Position Position Summary The primary responsibility of this position will be to ensure compliance to the Roche Pharmaceutical Quality System (PQS) quality assurance directives, global policies and standards. This role will be responsible for the development and implementation of QA review and monitoring processes to document on-going GBQC PQ...
Senior QA Specialist Requisition ID - 00432403 Description Position Summary The primary responsibility of this position will be to ensure compliance to the Roche Pharmaceutical Quality System (PQS) quality assurance directives, global policies and standards. This role will be responsible for the development and implementation of QA review and monitoring processes to document on-going GBQC PQS...
Description Position Summary The primary responsibility of this position will be to ensure compliance to the Roche Pharmaceutical Quality System (PQS) quality assurance directives, global policies and standards. This role will be responsible for the development and implementation of QA review and monitoring processes to document on-going GBQC PQS compliance and quality system effectiveness. In...
American Cybersystems Bothell, WA, 98021
Job Duties QA Doc Specialist provides documentation support by processing documents submitted into the master control system (internal document control system) for clinical and commercial manufacturing operations. This includes tracking, formatting, and issuing and distributing documents. They are also responsible for logbook issuance and filing / archiving documents in central records including ...
Description Senior Specialist, Clinical Quality Assurance (Contract) Medivation, Inc. (NASDAQ: MDVN – www.medivation.com) is a publicly traded biopharmaceutical company located in San Francisco. We are currently seeking a qualified, highly motivated, experienced individual for the position of Senior Specialist, Clinical Quality Assurance (Contract). This position’s main responsibility is to supp...

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