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- Lapeer, MI

ESSENTIAL DUTIES & RESPONSIBILITIES: Operate CNC Machine tools to manufacture high quality precision products. MACHINIST I – OPERATOR: Blue print reading including interpreting geometric dimensions and tolerances.Use inspection devise {calipers, micrometers, height gages, etc.}.Ability to complete daily logs, inspection forms, etc.Ability to perform tool changes, tool offsets, and tool wear offsets.Ability to perform work coordinate offsets to accommodate part datum variation for....


Minimum 10 years experience on Haas Vertical/Horizontal machining centers w/Fanuc controls.This Working Leader must be able to set-up; run and troubleshoot any/all situations for low-volume production work.The type of work we do ranges from automotive to aerospace. Job quantities from 25 to 500.Day shift. We offer competitive wage & benefits and typically work 50 plus hours/week.Job Type: Full-timeSalary: $20 to $25 Hr.Required education:High school or equivalentRequired experience:CNC....


CNC Lathe operator - $14-$16 hr. (based on exp.)Minimum of 1 year as an operator of a CNC LatheTool and insert changing experience.Qualifications:High school diploma or equivalent is preferred.Must be able to read and understand blueprints, shop orders and work instructions.Demonstrate general knowledge of machine shop practices and techniques and cutting tool basics.1 years set-up experience desirable.Must have strong math skills including the ability to work with fractions, decimals, and....

- Warren, MI

Summary: To operate & set-up programs on CNC Machines.Essential Duties and Responsibilities:Proficient with CNC LathesOperate & Set-up programs on the machines within the departmentIn addition to running machines, the Machinist will periodically inspect parts completed by operators during the production process to monitor for consistent dimensional and visual quality.Responsible for continuously monitoring equipment and tooling. In the event of a breakdown or other event that would....


Set-up CNC Lathes and Mills and Edit Machine (Speeds & Feeds)B. Assist Engineering Manager when directed.C. Assist employees when required.D. Manufacture of required parts.E. Attend meetings.G. Follow good housekeeping, organization routine.H Punch in and out daily.I Comply with the management operating systems procedures and instructions of J Follow all work and safety rules.K Participates in quoting process for machining areaL Trouble shoots process problemsP May be required to do setups

- Queens, NY

Summary Responsible for generating CNC Lathe programs for production as well as tooling. Also supporting the production machine shop with complete, accurate and cycle-efficient CNC programming which meets all customer and companies’ quality, productivity and safety requirements. Compensation is commensurate with experience.Duties and Responsibilities Develops, prepares, optimizes, and maintains CNC Lathe programs. Develop a concept for machining & set up on the machine. Develops, prepares,

- Rochester Hills, MI

SUMMARY: Responsible for the quality and hourly production goals of their assigned tasks, while working safely in a clean room environment.Directly responsible for ensuring thatproduction and inspection paper work is accurately completed and that all production and machine reject concerns are communicated to the maintenance tech and supervisor in a timely manner while following of the department’s processes and procedures along with the Company’s rules and regulations. Technicians must be able

- Rochester, MI

SUMMARY: To learn and assist in the maintenance and repair of all presses and equipment, while adhering to the Preventative Maintenance Program. POSITION RESPONSIBILITIES: · Develop and perform daily, weekly, monthly, and annual preventative maintenance. · Fabrication and repair of equipment. · Troubleshoot, fix and/or recommend all repairs, upgrades or improvements. · Order parts and call in any service technicians from outside companies as required. · Maintain records of maintenance....


The Clinical Trial Data Analyst is responsible for building programs to create datasets, listings, tables and figures from clinical databases, external data sources, and other sources. In addition, the position coordinates in-house data management activities (including vendor management) to ensure the accuracy and consistency of clinical databases for subsequent analysis and reporting. Responsibilities: Prepare data reports, tables and graphs for regulatory submissions, IRB submissions,....


This position is responsible for leading internal and outsourced Clinical Data Management activities in support of Clinical Research studies, managing the definition of Case Report Form (CRF) requirements, creation of the Data Management Plan, coordination of Centralized Data Review activities (a key component of Risk-Based Monitoring), and is accountable for data integrity, quality, and consistency at Database Lock. The employee must be able to lead data review activities and engage different


Education/ExperienceBS in life sciences or related field At least 2 years experience in clinical researchKnowledge of FDA regulations Prior Study Start-Up experience preferredAdvanced skills in Microsoft Word, Microsoft PowerPoint, Microsoft Excel, Microsoft Outlook Experience with Adobe Acrobat Professional and Microsoft Access a plusPresentation Delivery ResponsibilitiesExecute study start-up for assigned protocols within company timelines by identifying clinical team needs, Oversee Site....

- Cambridge, MA

Global Company is hiring a Senior Leader Clinical Operations Biotechnology company specializing in the detailed structural analysis of complex drugs and is headquartered in Cambridge, MA. Company is applying its technology to the development of generic versions of complex drugs, biosimilar and potentially interchangeable biologics, and to the discovery and development of novel therapeutics for oncology and autoimmune indications This position will be responsible for initiating and leading....

- Irvine, CA

The candidate is responsible for expeditiously developing and processing raw material and product documentation to meet quality requirements within timelines established for product launch and/or timely project completion.The Master Specifications and Documentation department interacts with various Pharmaceutical groups within the organization and departments such as Quality, Global Pharmaceutical Technology, Regulatory Affairs, Operations, Manufacturing (all sites), Procurement (Sourcing),....


The specialist will work with a team of medical information professionals to capture unsolicited medical inquiries from health care professionals, consumers, and corporate business partners. Also, research and respond to requests for scientific/medical information using various search and retrieval techniques and medical literature database (product label, published and unpublished studies) to develop a medical/scientific response that is accurate, fair balanced, complete and delivered in a....


The Associate will be responsible for supporting CTM/OSL and ensuring that all assigned clinical study(ies) are running on time and on budget and are completed in compliance with all relevant laws, regulations, and regulatory guidelines as well as all policies and procedures. Requirements: Bachelor’s degree or higher (science degree preferably in science or health-related field) Previous experience of working on a clinical study 1-2 year relevant experience in pharmaceutical industry or CRO....

- Woodstock, ON

This company has holiday weekends that are 4 days long insead of 3, celebrating 14 statuary holidays instead of the typical 9 and have a good pension plan to boot? It is a well respected company, great place to work low employee turnover and having positive Employee/Labour Relations. Part of a Large multinational corporation with a worldwide presence this is a mid-sized plant with some unique processes manufacturing products for a wide range of industries Offered is the opportunity to work....


EDUCATION/EXPERIENCE: - 1+ years of relevant experience in pharmaceutical industry - Science degree in medical or health-related field - Clinical Trial Support/Clinical Study experience - Work effectively in a team/matrix environment - Handle conflict management and resolution RESPONSIBILITIES: - Ensuring that clinical studies are run on time and budget - Ensure compliance with regulatory guidelines - Management of clinical trial documentaiton - Tracking of various clinical trail resources

- Waupin, WI

Provision of pharmaceutical services for offenders in Wisconsin's correctional system through the Bureau of Health Services Central Pharmacy Service in a manner consistent with professional standards and comparable to services delivered in non-correctional settings. Prepares, fills and dispenses prescriptions for drugs, chemicals and supplies on receipt of a proper order from a prescribing practitioner for an inmate/student. Prepares and fills extemporaneous prescriptions and orders....


Background and Objective:The mission is to serve the community by helping people access affordable housing by working with our collaborative partners, we develop, renovate and maintain housing, promote neighborhood revitalization and assist residents in accessing needed social services. They maintains several enterprise and departmental applications and platforms, including housing software (PHAMS). In addition, they have an in-house Information Technology department that includes database and


The position is responsible for planning and preparing complex medical device regulatory submission documents for US, Canada, and EU regulatory filings. Provides support for other global regulatory filings. Utilizing detailed, in-depth understanding of medical device regulation leads anticipates in goal regulatory teams, interprets regulations, and provides regulatory guidance. Support management with regulatory programs planning and implementations of departmental strategies and policies.

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