Biotech Validation Jobs

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145 Biotech Validation jobs found on Monster.

Jobs 1 to 20 of 145
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply Quality Lab Associate I Los Angeles, CA Full-Time $75,000 - $90,000 Apply Apply Quality Lab Associate I Los Angeles, CA Full-Time $75,000 - $90,000 Apply Job Details If you are a Quality Lab Associate with experience working with Assays, please read on! Founded in the early 1900's, we are an American based le...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply IT Manager- BioTech / Pharmaceutical Cambridge, MA Full-Time $100,000 - $120,000 Apply Apply IT Manager- BioTech / Pharmaceutical Cambridge, MA Full-Time $100,000 - $120,000 Apply Job Details Based in Cambridge, MA, we are a growing Biotech Company looking to hire an experienced hands-on IT Manager who can hi...
Summary: A company specializing in high level contract services management and biotechnology support to emerging companies in the field of cellular and biological therapeutics is seeking a Manufacturing Associate. Responsible for performing various manufacturing activities related to the start-up and GMP production of a number of novel cellular products. Including but not limited to; assisting in...
Auto req ID: 2151BR Job Posting Title: Project Manager Validation Person Type: Regular 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 discovers, invents, develops, manufactures, and commercializes medicines for...
Description PSC Biotech has a need for a Decommissioning/Validation Engineer for a long term project (6 months to a year +) in the New Jersey area. Responsibilities Decommissioning engineer must have the ability to develop decommissioning protocols (IQ/OQ), decommissioning reports, and test documents. Good writing/grammar skills and attention to detail are essential. Decommissioning facilities/uti...
Process - Validation Engineer ( fulltime) A strong background with process design in the Biotech / Pharmaceutical industry; supervise equipment installation, start-up and qualification; evaluate and selecting equipment; write technical specifications; looking for someone with an engineering degree and 2+ years of experience; some travel required; if interested send resume in word format: Skills: A...
The Validation Engineer is responsible for the execution and management of qualification activities for equipment and facilities on site. The engineer prepares and executes qualification and re-qualification activities as necessary for new and modified equipment and / or facilities so that the qualification status of site equipment is maintained at all times. The engineer also assists external qua...
The Validation Engineer is responsible for the execution and management of qualification activities for equipment and facilities on site. The engineer prepares and executes qualification and re-qualification activities as necessary for new and modified equipment and / or facilities so that the qualification status of site equipment is maintained at all times. The engineer also assists external qua...
Auto req ID: 2002BR Job Posting Title: Validation Specialist Person Type: Regular 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 discovers, invents, develops, manufactures, and commercializes medicines for the t...
Job Details: Validation Engineer - commissioning - qualification "Experience with biotech (cell culture, bioreactors, filters, centrifuges, chromatography/purification, water for injection, clean steam, autoclaves)" W2 rate with a $4100.00 a month per diem Skills and Knowledge: Facility qualification / validation and must understand commissioning / qualification and adhere to validation and qualit...
Auto req ID: 1869BR Job Posting Title: Software Validation Project Manager Person Type: Regular 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 discovers, invents, develops, manufactures, and commercializes medic...
Barry-Wehmiller Design Group provides engineering and technology services to the world’s leading companies through the efforts of over 800 engineering and technical specialists. We are focused on providing our professionals with opportunities for leadership and career advancement within a thriving work environment and a unique “people-centric” culture. We offer a robust, centralized learning and d...
VALIDATION / QUALITY ASSURANCE WITH BIOPHARMACEUTICAL REQUIREMENT #14-00752 RECRUITER: BRIDGET BURNS JOB LOCATION: DEVENS, MA JULY 24, 2014 Project Description: Provide Quality Assurance oversight in the following areas to include but not limited to: · QA review and approval in the deliverables associated with the development and execution of remediation plans to align the abatacept drug substance...
POSITION SUMMARY: Leadership role for validation group supporting processes (including CIP/SIP), equipment, facilities/utilities and computerized systems for sterile products, devices, and packaging. Responsibility also includes strategy for site validation master plan, risk assessments, periodic assessments, commissioning for new capabilities, and product/process technology transfers. ESSENTIAL J...
Primary Duties: Under the direction of the Head of CSV and Process Compliance, the primary responsibility of the CSV Lead will be to support the R&D Quality Assurance & Compliance function by assuming primary responsibility for implementing, managing and/or coordinating R&D QA&C support of computer system validation (CSV) activities to GxP and Shire standards (SDLC); advising the R&D IT Business P...
Equipment Validation Engineer Duties & Responsibilities: Lead/manage validation projects including: Provide risk assessment for new systems and changes to existing systems Write validation plans, protocols and reports Execute and provide reviews of validation protocols and validation periodic monitoring Lead or participate in project team including the supervision of validation contractors Provide...
The position will support the development of a new, state-of-the-art plasma fractionation facility that will bring Baxter additional capacity for testing, purification, and fill and finish for its biologic medications. Responsible for technical support of the Commissioning, Qualification and Validation (CQV) Program at the Baxter Covington, GA facility, specific to Facilities, Utilities, and Equip...
A large multi-national nutrition company is seeking a Validation Engineer to lead the overall quality and compliance activities of their computer systems. The candidate must have experience with validating manufacturing systems. Specific experience with PLC’s, DCS systems and HMI systems. The candidate will support GMP and ISO activities and must have detailed knowledge of these technical areas. U...
Responsibilities: We are seeking a highly motivated cell biologist to generate novel antibody-based therapeutics utilizing our industry-leading ADC technology. The successful candidate will independently design, conduct, and interpret experiments utilizing a diverse array of techniques aimed at validating targets and characterizing ADCs. Standard methodologies will include cell-based assay develop...
ARGOS IS GROWING! Argos Therapeutics is a biopharmaceutical company focused on the development and commercialization of fully personalized immunotherapies for the treatment of cancer and infectious diseases based on its Arcelis™ technology platform. We are currently seeking a well-qualified Methods Validation Manager. SCOPE: Implement and manage the method validation program for Quality Control as...
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