Biotech Validation Jobs in Littleton, Massachusetts

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14 Littleton, MA Biotech Validation jobs found on Monster.

Jobs 1 to 14 of 14
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...
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...
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...
Position Details: Position: Sr. Quality Engineer Location: Devens, MA, 01434 Duration: 6+ Months Contract (40 hrs/week and expected payable OT Hours) Description of Services: Orencia Technical Remediation – Validation Workstream and Elotuzumab Provide Quality Assurance oversight in the following areas to include but not limited to : · QA review and approval in the deliverables associated with the...
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...
Primary Role: •The Senior Automation Engineer I for Building Automation will help improve the efficiency and effectiveness of the Engineering Technical Services Group (ETS) by contributing towards infrastructure and system improvements, policies, guidelines, procedures, standards and cross-functional business processes. The candidate should have a mindset of knowledge sharing, major contributor in...
RESPONSIBILITIES: Our client in Framingham MA in the Biotech industry is looking for a R&D Project Manager/Business Analyst for a 6+ Month project. The R&D IS Project Manager/Business Analyst will be responsible for leading one or more small R&D Lab Systems project deliveries. He or she will be responsible for leading a small project team on project activities, the scope include by not limited to...
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...
TAKE Life Sciences are domain experts in the areas of Clinical, Regulatory, Safety and Compliance and are motivated by the success of our clients. We pride ourselves on our industry insight, our simplification approach and our pragmatic solutions which improve outcomes, ensure compliance and enable growth. Our capabilities cover strategic and change management consulting, technology and BPO. The U...
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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