Biotech Validation Jobs

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869 Biotech Validation jobs found on Monster.

Jobs 1 to 20 of 869
Description CSC has an immediate position for a Process Validation Manufacturing Manager. The Process Validation Manufacturing Manager provides leadership and technical expertise to the DVC product teams and DVC subcontractors with regard to development, design, optimization, qualification, validation and execution of manufacturing processes and analytical methods compliant with the current Food ...
Description CSC has an immediate position for a Sr. Process Validation Manufacturing Manager. This person will provide leadership and technical expertise to the Dynport Vaccine Company (DVC) product teams and DVC subcontractors with regard to development, design, optimization, qualification, validation and execution of manufacturing processes and analytical methods compliant with the current Food...
Oct 24, 2014 CSC has an immediate position for a Sr. Process Validation Manufacturing Manager. This person will provide leadership and technical expertise to the Dynport Vaccine Company (DVC) product teams and DVC subcontractors with regard to development, design, optimization, qualification, validation and execution of manufacturing processes and analytical methods compliant with the current Foo...
Description CSC has an immediate position supporting Dynport Vaccine Company (DVC) for a Manager, Analytics and Validation. The qualified candidate will provide leadership and technical expertise to the DVC product teams and DVC subcontractors in regard to the development, qualification and validation of analytical methods used for in-process, lot release and/or stability testing. The qualified c...
Description CSC has an immediate position for a Sr. Process Validation Manufacturing Manager. This person will provide leadership and technical expertise to the Dynport Vaccine Company (DVC) product teams and DVC subcontractors with regard to development, design, optimization, qualification, validation and execution of manufacturing processes and analytical methods compliant with the current Food...
Jul 23, 2014 CSC has an immediate position for a Process Validation Manufacturing Manager. The Process Validation Manufacturing Manager provides leadership and technical expertise to the DVC product teams and DVC subcontractors with regard to development, design, optimization, qualification, validation and execution of manufacturing processes and analytical methods compliant with the current Food ...
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...
Responsible for executing and enhancing the validation program at a large scale, multi-product, GMP biotech contract manufacturing facility. Managing and planning the work of the entire department. Assessing workload and managing resource deployment to achieve validation goals. Responsible for managing and tracking execution of validation activities versus project timelines. Develop validation m...
Our client, an emerging NC-based biotech that is performing breakthrough research in the field of regenerative medicine, is actively recruiting for a very sharp, detail-oriented and quality-oriented scientist, with some bkgd performing cell culture work in industry, to join its award-winning R&D team. Company is developing a highly anticipated portfolio of tissue-engineered products. This Researc...
Our client, an emerging NC-based biotechnology company that is performing breakthrough research in cancer and infectious disease treatment, is actively recruiting for a very bright and capable team player for a key role on its bioprocessing team. This is an excellent foot-in-the-door opportunity for a high potential candidate, with some background in manual cellular aseptic production, to join an ...
Must have: •B.S./M.S. degree in an engineering/scientific field •Minimum of 8+ 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, sterilization and controlled temperature unit val...
Must have: •B.S./M.S. degree in an engineering/scientific field •Minimum of 2-4 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, sterilization and controlled temperature unit va...
16471 ) Validation Engineer - III Must have: - B.S./M.S. degree in an engineering/scientific field - Minimum of 5+ 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 steriliz...
Our client of 8 years, is a Pharmaceutical Company recognized globally for their unparalleled development and manufacturing services for the world’s leading pharmaceutical, biotechnology, and healthcare companies. With four cGMP facilities and over a million square feet of state-of–the-art manufacturing, packaging, and distribution space, our client offers full service outsourcing solutions inclu...
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 ...
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 ...
Only local San Francisco Bay area candidates! Direct W2 employees only! No 3rd party agencies! Duration: 6 - 18 months The candidate must have the ability to work in a team composed of validation professionals and on a cross functional project team. This candidate will be a creative, solution-minded thinker that has the ability to quickly adapt in a fast-paced, highly regulated environment. * ...
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 medicine...
Our client is looking for 5 Project Managers for a 6+ month contract opportunity in Vernon Hills, IL. Required: 5+ years’ experience as a Project Manager Experience with computer systems validation and testing Experience with pharma or biotech industry Must understand the validation lifecycle within a pharma/biotech environment Experience creating project scorecards Experience with project ...
Description CSC has an immediate position for a Formulation/Fill/Finish Manager, supporting Dynport Vaccine Company (DVC). The Formulation/Fill/Finish Manager provides technical oversight of these activities to CMO subcontractors across vaccine development programs. This position is located in Frederick, Maryland. Essential Job Functions Provide leadership and technical expertise to the DVC pro...

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