Search Results: 132 vacancies
...and enzymes for complex diagnosis and prognostic markers Contribute to corporate strategy for additional regulatory approvals (CAP, FDA, ) relating to GHI Histopathology Assess the quality of slide preparations and troubleshoot procedures if necessary Prepare control slides...
Suggested
Permanent employment
Full time
...collection, including donor set-up, donor monitoring and donor disconnect.
2 In compliance with SOPs and Food & Drug Administration (FDA) guidelines, performs venipuncture on donors to begin pheresis process.
3 Evaluates vein performance of the donor to identify...
Suggested
Holiday work
Full time
Temporary work
Local area
Immediate start
...training (e.g. Rapid Software Testing, Black Box Software Testing)
Software verification of medical devices and working knowledge of FDA Quality System Regulation
At Beckman Coulter Life Sciences we believe in designing a better, more sustainable workforce. We...
Suggested
Part time
Remote job
Flexible hours
...aggressive schedules.
Understanding business, legal and regulatory requirements with the ability to learn regulatory requirements, FDA 21 CFR 820/GMP Medical Device Regulations.
Key Performance Objectives
Short Term: (0 to 3 months)
Learn about Kimball Vision...
Suggested
Contract work
Temporary work
Local area
...documentation as needed.
Qualifications:
Relative Work Experience: 5-7 years related work experience (manufacturing experience in a FDA/ISO facility preferred).
Education: High School diploma
Certifications / Licenses: ASQ CQI pr CQT preferred.
Computer...
Suggested
Work experience placement
...Enterprise Resource Planning (ERP) systems is a must have
~ Knowledge of quality assurance standards relating to medical devices, FDA experience would be helpful.
~ Work with metrics as a result of our high speed production demands and planning.
~ Communicate with...
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Contract work
Temporary work
Local area
Shift work
Night shift
Day shift
Afternoon shift
All shifts
...refrigerator charging
Final Test
Wiring
Record measurements as needed. Ensure that device history records are completed according to FDA GMP requirements. Complete nonconformance records according to established procedures and GMP requirements.
Troubleshoot equipment...
Suggested
Work from home
Shift work
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...Skills Preferences:
Associates Degree in Electronic/Electrical/Automation engineering
Experience within a regulated industry; FDA regulated industries preferred
Ability to perform quality work without close supervision
Proficiency in CMMS (e.g., GMARS), Microsoft...
Suggested
Temporary work
H1b
Weekend work
Day shift
...Perform daily safely inspections per the Safety Checklist on forklift trucks
Ensure facility is inspection ready at all times for SQFI, FDA, and customer needs.
Communicate and report any incidents to supervisor
Ensure product rotation procedures are followed....
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For contractors
Shift work
...schooling when required.
Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.).
Requirements
High school diploma or GED equivalent is required....
Suggested
Holiday work
Work experience placement
Outdoor
Flexible hours
Shift work
Monday to Friday
...confidential information. required
Demonstrated knowledge of current Good Manufacturing Practices, Food and Drug Administration (FDA) regulations, and AABB standards related to blood center operations and collection requirements. required
Possess the following: *...
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Flexible hours
...as required. Understands work environment issues (i.e. OSHA regulations, etc.).
Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive...
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For contractors
Shift work
...Cleaning, Cleanroom, Quality assurance, Food safety, cip, Manufacturing, Production, Machine operator, Sanitation, Quality control, FDA, Blender, Mixer, Batch Mixer, Quality Tech, Quality Test, Quality Technician, pH Test, haacp
Additional Skills & Qualifications:...
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Immediate start
...data, and reports, as well as support the management and maintenance of regulatory correspondence with regulatory agencies such as the FDA and NRC.
Manage and maintain confidential files and records.
Participates in and/or coordinates functions, meetings,...
Suggested
...complaints), and initiates applicable corrective measures
Ensure compliance to all applicable regulatory agency requirements (USDA, FDA, CFIA) and liaison with local food regulatory officers.
Provide leadership for compliance to food safety and quality programs Implements...
Suggested
Local area
Remote job
Relocation package
Flexible hours
...activities accurately and in a timely manner;
Responsible for the safekeeping of all medication stock and the records required by the DEA, FDA, and ADP;
Dedicates a minimum of 90% of regularly scheduled work hours to activities directly related to the administration of...
Full time
Local area
Shift work
Saturday
Early shift
...policies, procedures and regulations. Must ensure maintain operational compliance with U.S. and international regulatory agencies (i.e. FDA, EU, ISO, USP, NRC, etc.) In addition, must supply the highest level of both internal and external customer service and measure and...
Holiday work
Contract work
Work experience placement
Outdoor
Shift work
Monday to Friday
...position also provides appropriate documentation to meet the strict requirements set by the Indiana State Department of Health, ACR, MQSA/FDA.
Essential Functions and Responsibilities
Proactively contributes to Eskenazi Health's mission: Advocate, Care, Teach, and...
Part time
Local area
Shift work
...The required qualifications for the job include:
Education required: High School Degree with 5+ years of experience in a regulated (FDA, ISO, or GMP) manufacturing setting.
Experience required: 2+ years in Quality Assurance or Quality Control.
It would be a...
...experience as a Validation Engineer, Quality Assurance Engineering, or Quality Validation Consultant working with 21 CFR 210, 211 in the FDA regulated industry (Pharmaceutical or Medical Device).
~ Experience with equipment qualification, software validation, test method...
Contract work
Temporary work
Work experience placement
Local area
Flexible hours
