Biotech Validation Jobs in Littleton, Massachusetts

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12 Littleton, MA Biotech Validation jobs found on Monster.

Jobs 1 to 12 of 12
Primary Duties: The Engineering Manager will lead and drive the process services engineering function supporting process support areas in the manufacturing of commercial and clinical products across multiple Shire sites. The process services engineering function covers all equipment and systems related to: •Solution preparation (media and buffer) •Clean-In-Place (CIP) skids and processes •Equipmen...
Job Description : Ability to manage multiple and varied tasks with enthusiasm and prioritize workload to meet strict deadlines. Serve as functional liaison between the technical team(s) and internal and clients Client focused approach to work and the ability to analyze and interpret client needs. Ability to travel when client facing work is required Ability to clearly document business and technic...
PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed sig...
Our client has an immediate need for a Quality Engineer (Job# 14-00912) A national, award winning healthcare provider with a dedication to clinical excellence has partnered with RCM to drive business critical projects throughout 2014. If you are a Quality Engineer Professional looking for a long-term contract with an industry leader and a potential career opportunity with RCM’s growing New England...
Primary Role: The Senior Automation Engineer II will improve the efficiency and effectiveness of ETS by making significant contributions towards infrastructure improvements, policies, guidelines, procedures, standards and cross-functional business processes. The candidate should have a mindset of knowledge sharing, lead design reviews across the portfolio of departmental projects, and contribute t...
Quality Control Senior Specialist Growing client in the Lexington/Waltham Area is looking for Senior Quality Control Specialist that will provide support and performing in vitro cell-based experiments for validation of new assays and analysis of product lots. Responsibilities of the Senior QC Specialist: • Perform QC assays including Real Time RT-PCR, DNA and SGAG quantification, SDS PAGE, pH, Osm...
Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis. Title: Associate Scientist II, Histotechnologist Job ID: 5446 Industry: Biotech/Pharmaceutical Location: Cambridge, MA Duration: 12 Month Contract Pay Rate Range: Depends on Experience (...
Purpose / Summary Provide managerial leadership to ensure the safe, compliant and cost effective management and administration of engineering department documentation in support of LMI facility, process, and manufacturing operations. Is Accountable to independently plan, organize, lead and control all aspects of ownership of LMIs engineering documentation. This role exhibits the competent leadersh...
Primary Role The individual will work in the Supplier QA sub-group of Shire Human Genetic Therapies Quality Assurance Department. This unit oversees contract manufacturing (3rd party manufacturing) operations, supply chain operations and supplier quality functions performed on behalf of Shire. This position supports the execution of quality systems including the external audit program. This positi...
The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas. In fact, Quintiles conducts more clinical trials than anyone else in the world. Become involved in work that improves the quality of life for people around the globe. Let your...
Document Security Administrator- QA Location: Cambridge MA We are currently looking for an individual who can play a key role in the configuration, implementation, and ongoing oversight and management of an electronic document management system. This individual will be instrumental in configuration of the system and workflows and provide ongoing system administrator, file maintenance, and user sup...
Title: Associate Scientist I, Technical Development Job ID: 5445 Industry: Biotech/Pharmaceutical Location: Cambridge, MA Duration: 12 Month Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate) Job Details: The Associate Scientist I will perform routine and complex assays for analysis of preclinical, clinical and research samples and related duties such as quality control, sampl...
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