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Device Quality Engineer for software devices to help coordinate resources and activities for the Quality function supporting commercial software applications classified as medical devices including, but not limited to, supporting all phases of in-house and/or outsourced design and development as well as product support processes.Represent Quality function as designee on the cross-functional Global Development Team (GDT)where strategy includes development of commercial software devices....


OverviewThe company is proud to have been recognized as one of The Boston Globe’s Top Places to Work in 2015, 2016 and 2017. Responsible for leading Process Automation System (PAS) implementation at new Greenfield facility. Work with cross-functional teams on developing system requirements, managing System Integrator project to implement and test, and oversight of all Commissioning and Qualification needs during facility startup. Assist in overall company standards and capital planning around....


Our firm is in search of an experienced Ambulatory Surgical Center Administrator for an Ambulatory Surgical Center in Oregon located about 2 hours from Portland and an hour south of Salem. This location puts you an hour from the coast and an hour from the mountains! Excellent environment offering a unique work/ life experience. The qualified candidate must come from an ASC setting and have Five to Eight years ASC leadership expereince. This position reports to the CEO and you will have....

- Shelbyville, IN

Electrical Engineer SE Indianapolis (30 mi from 465) - Greater Shelbyville IN Area Competitive Salary, Bonus, Profit Sharing, Excellent Benefits Our client is a privately held global Tier 1 automotive component manufacturer with well known customers like Honda, Toyota, Subaru, as well as many others. They have a large facility just southeast of Indianapolis by about 45 minutes; where they have 500 employees at two ISO-certified facilities on 60+ acres (union facilities). They are committed


Global Specialty Pharmaceutical company in Bridgewater, New Jersey is looking to hire a Manager of Clinical Quality AssuranceThe Manager Clinical Quality Assurance is a key member of the company Research and Development organization. This role is responsible for Clinical QA activity related to the planning, conduct, and reporting of GCP audits in order to ensure that clinical studies are conducted in compliance with applicable regulations, guidelines and company standards. This role also has....


The Manager, Medical Information will assist in the operational oversight of medical information within the Medical Affairs function under the guidance of the Lead of Medical Information. The manager will be responsible for providing and supporting the provision of accurate, scientifically balanced and timely responses to inquiries received from health care professionals, consumers and other customers. The manager will monitor the scientific literature and communicate new data to relevant....

- Lynchburg area, VA

QUALITY SYSTEMS MANAGER- Lynchburg, VA Area Our Client, A Global Fortune 500 has been well recognized as one of the world's most respected names for Healthy Nutritional/ Food Products. Due to a recent promotion and additional new state of art high volume packaging lines, the Lynchburg, VA area plant is looking for a QUALITY SYSTEMS MANAGER to manage and improve the ongoing batch log auditing and product release system, manage and improve plant quality control systems including document change....


Senior Manager of Quality Control (Reagent / IVD / Assay Development) Walpole, MA Competitive pay, Bonus, Excellent benefits This role is with a global leader in medical technology (imaging, diagnostics, healthcare IT), an organization dedicated to ongoing success by hiring top talent, investing in R&D, and commitment to engineering excellence for over 100+ years. We currently have an opening for a Senior Manager. This role is focused on Control System Improvements; Design Quality....


JOB DUTIES IN ORDER OF IMPORTANCE:(These duties are illustrative only. Incumbents may perform some or all of these duties or other job-related duties as assigned.)May be required to work at more than one institution. Provides program direction by acting for superior & by relieving superior of most difficult administrative duties; organizes, plans, develops & implements a comprehensive medical, mental health & recovery services quality assurance evaluation & monitoring program....

- Richmond, VA

We are seeking a Purchasing Director ready to make a move to a challenging role for a very people oriented company. They are seeking a purchasing leader with success with cost control in an inflationary market and experience with a complex product mix.This people oriented company is a large growing industrial distribution supplier within several verticals in industrial manufacturing. The Purchasing Director with have oversight of multiple locations with 10 direct reports within purchasing and....

- Buffalo, NY

Clinical Project Manager As a Clinical Project Manager (CPM), you will work in a matrix management environment and serve as the primary contact for interdepartmental and external study contacts. This experienced CPM role is responsible for managing all stages of a clinical study within GCP and ICH guidelines when direct management by the sponsor is required. The CPM may also function as the liaison and provide support for sponsor managed studies in an international setting, and, may oversee....


Clinical Research Associate POSITION OBJECTIVE: Work within a clinical team setting to ensure compliance with protocol and overall clinical objectives. Essential Job Functions/ResponsibilitiesParticipates in the preparation and/or review of draft protocol and informed consent documentsPossesses detailed knowledge of the study protocol and its associated activities and timelinesParticipates in conference calls, prepares agenda and summariesCoordinates with project team and other study personnel


Clinical Research Associate POSITION OBJECTIVE: Work within a clinical team setting to ensure compliance with protocol and overall clinical objectives. Essential Job Functions/ResponsibilitiesParticipates in the preparation and/or review of draft protocol and informed consent documentsPossesses detailed knowledge of the study protocol and its associated activities and timelinesParticipates in conference calls, prepares agenda and summariesCoordinates with project team and other study personnel

- Buffalo, NY

Senior Clinical Research Associate POSITION OBJECTIVE: Work within a clinical team setting to ensure compliance with protocol and overall clinical objectives. Essential Job Functions/ResponsibilitiesParticipates in the preparation and/or review of draft protocol and informed consent documentsPossesses detailed knowledge of the study protocol and its associated activities and timelinesParticipates in conference calls, prepares agenda and summariesCoordinates with project team and other study....

- Cranford, NJ

Senior Clinical Research Associate POSITION OBJECTIVE: Work within a clinical team setting to ensure compliance with protocol and overall clinical objectives. . Essential Job Functions/ResponsibilitiesParticipates in the preparation and/or review of draft protocol and informed consent documentsPossesses detailed knowledge of the study protocol and its associated activities and timelinesParticipates in conference calls, prepares agenda and summariesCoordinates with project team and other study....

- Indianapolis, IN

Tooling Engineer SE Indianapolis (30 mi from 465) - Greater Shelbyville IN Area Competitive Salary, Full Benefits + Bonus 401K + Profit Sharing, PTO Our client is a privately held global Tier 1 automotive component manufacturer with well known customers like Honda, Toyota, Subaru, as well as many others. They have a large facility just southeast of Indianapolis by about 45 minutes; where they have 500 employees at two ISO-certified facilities on 60+ acres (union facilities). They....

- San Francisco, CA

Scope of Work:The Contractor will independently provide services to satisfy the overall operational objectives of the United States Attorney’s Office, Northern District of California. Contractor services are required to support the administrative needs of everyday technical tasks by supporting the Information Technology (IT) staff and assisting to solve minor computer-related problems. Support is required largely in the Administrative Division’s Information Technology (IT) Section to provide....

- Southern, CT

Minimum Requirements: B.S. Chemical Engineering; 5+ years of experience out specialty chemicals, continuous chemicals or food additives. This is a small and growing manufacturing site so the more of the following pluses the better; a strong chemistry knowledge, design through installation of projects ($50K+), CAD, Six Sigma, PMP, process optimization, small-scale batch reaction, distillation, centrifugation, and filtration, Job Description: Our client is a rapidly-growing producer of....


Growing town, global company, strong career opportunity! The company is offering a strong base salary, excellent annual bonus, strong relocation assistance, retirement funding and more! We are working with a client that is a $2.5 billion global provider of distinctive, high quality ingredients and solutions to the food, beverage and related industries. With their large-scale, efficient manufacturing plants, they use innovative technology to turn raw materials into distinctive, high quality....


We are looking for a Controls/Manufacturing Engineer with 3-5 years of applied professional experience in electrical process control, instrumentation, automation and computer and data communication systems in a manufacturing environment. Job Responsibilities: Support the maintenance/ICT department on technical issues to decrease downtime and increase production efficiency through timely maintenanceDesign and implement test plans to validate that equipment meets functional requirements and....

321-340 of 351 results