Biotech Validation Jobs

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146 Biotech Validation jobs found on Monster.

Jobs 1 to 20 of 146
Title: Engineer PE Upstream Job ID: 23615 Industry: Biotech/Pharmaceutical Location: West Greenwich, RI Duration: 17 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate) Job Details: Provide technical support of cell culture processes for commercial manufacturing at manufacturing sites or contracted manufacturing sites including process performance monitoring; implementati...
Our client, a rapidly-expanding biotech company with headquarters in Research Triangle Park, NC, is actively recruiting for a highly skilled and knowledgeable Scientist with strong background in Manufacturing and Production for a key role on its growing team. Company is developing a portfolio of emulsion products that are highly anticipated by industry leaders. Certain products are nearing commerc...
Description PSC Biotech is one of the world's largest compliance consulting firms specializing in compliance consulting in the life sciences industry. We are seeking three (3) Utilities Verification (Validation) Engineer resources to work with our client in Seattle, Washington. Responsibilities The Verification Engineer will be responsible for functioning as an individual contributor. The assignme...
Major biotech companyis looking for a Software Quality Assurance Engineer with deep experience in Software Quality Assurance and Computer System Validation. The candidate must possess the ability to work on a cross functional project team and with other members of a Quality Assurance and System Validation sub team. This candidate will be a creative, solution-minded thinker that has the ability to...
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: 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...
Overview: We are looking for a scientist/engineer to fill the role of Director of Process Validation in our Hampton, NJ facility. Individual responsibilities include: Involvement in technology transfer, new product scale-up, and process optimization of biopharmaceutical manufacturing processes. Oversee and manage manufacturing process validation activities at drug substance and parenteral drug pro...
Barry-Wehmiller Design Group provides engineering and technology services to the world’s leading companies through the efforts of over 700 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...
The Sr. Validation Specialist focus will be on Facility and Equipment Validation responsibilities, using knowledge and previous experience with Equipment and Processes used in Biotech/Pharmaceutical Manufacturing facilities. Filtration skids, Columns, CIP/COP skids and processes, Centrifuges, Bulk Filling, Cleaning Validation and Optimization, and SIP processes, where several tanks and related tra...
This position supports the LAMP B 8 manufacturing facility start-up through the qualification and/or validation of equipment, computerized systems, facilities, critical systems, materials, and manufacturing processes. Validation activities include research, protocol writing/execution and final report generation. Additionally, investigations of manufacturing challenges are conducted and process imp...
Applies thorough understanding of cGXPs, relevant SOP curriculum, routine project procedures, project management, and other training as appropriate. Partners with Engineering/Process Engineering/Automation to ensure smooth and efficient execution of testing strategies through the implementation of qualification and commissioning plans for process control systems. Handles projects that are more com...
Must have: Education: BS/MS engineering/scientific field Skills: - Minimum of 2 years post-Bachelors degree experience in a cGMP environment (e.g. Production, Development, Process Engineering, Technical Services or related field) in pharmaceutical/ biotech industry - Previous experience with equipment validation, specific experience with cleaning and sterilization validation required. - Role requi...
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...
Auto req ID: 1257BR 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...
VALIDATION ENGINEER III - 33564 Description Genzyme has pioneered the development and delivery of transformative therapies for patients affected by rare and debilitating diseases for over 30 years. We accomplish our goals through world-class research, collaboration with the global patient community, and with the compassion and commitment of our employees. With a focus on rare diseases and multiple...
Auto req ID: 1799BR Job Posting Title: Process Sciences Associate (Process 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 commerci...
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...
Our client is currently seeking a SENIOR QUALITY SYSTEM VALIDATION SPECIALIST. This job will have the following responsibilities: Experience with medical device regulations, control software compliance, and define test strategies. Candidates are validation, quality, and regulatory in medical device regulations, control software compliance, and define test strategies. 6-10 years validation experien...
Barry-Wehmiller Design Group provides engineering and technology services to the world’s leading companies through the efforts of over 700 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 Specialist - Engineer "Validation (CQV) experience in writing and executing documents with experience in purification (chromatography), filtration, overall downstream processing for biotech equipment" Knowledge: Facility qualification / validation and must understand commissioning and adhere to validation and quality guidelines. Familiar with support systems, bioprocess unit operations,...
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