Search Results: 270 vacancies

 ...experience with a beverage, food or liquid consumer products manufacturer is preferred. Prior knowledge of GMP’s, sanitation standards and FDA requirements is helpful. Must be able to stand for extended periods of time – 12 hour shifts. Basic math skills are needed.... 
Suggested
Hourly pay
Flexible hours
Shift work
Night shift

Premium Waters

Kentland, IN
8 days ago
 ...CPR) and AED certification   Fulfill state requirements (in state of licensure) for basic IV therapy   Satisfactorily complete the FDA approved training requirements for BioLife Medical Support Specialist   Two years in a clinical or hospital setting   What... 
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Hourly pay
Minimum wage
Holiday work
Full time
Temporary work
Seasonal work
Local area
Remote job

Biolife Plasma Services

Elkhart, IN
1 day ago
 ...glove wear PREFERRED QUALIFICATIONS: Associates or Bachelor’s Degree Experience working with SOPs, GDP, GMP, CLIA, and the FDA Experience working in a highly regulated or high-volume retail environment Excellent interpersonal, organizational, technical,... 
Suggested
Minimum wage
Holiday work
Full time
Temporary work
Traineeship
Local area
Remote job
Relocation
Shift work
Afternoon shift

Biolife Plasma Services

Bloomington, IN
2 days ago
 ...glove wear PREFERRED QUALIFICATIONS: Associates or Bachelor’s Degree Experience working with SOPs, GDP, GMP, CLIA, and the FDA Experience working in a highly regulated or high-volume retail environment Excellent interpersonal, organizational, technical,... 
Suggested
Minimum wage
Holiday work
Full time
Temporary work
Traineeship
Local area
Remote job
Relocation
Shift work
Afternoon shift

Biolife Plasma Services

Bloomington, IN
9 hours ago
 ...continuing review/amendments/close out information; schedules and prepares for monitor visits; prepares and responds to Sponsor and/or FDA audits. Stays up-to-date and maintains current knowledge of regulatory affairs and/or issues; maintains a high level of expertise... 
Suggested
Holiday work
Full time
Work experience placement

Indiana University

Indianapolis, IN
4 days ago
 ...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... 
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Holiday work
Full time
Temporary work
Local area
Immediate start

CSL Plasma

Indianapolis, IN
9 hours agonew
 ...communication capabilities especially in liquid/aerosol packaging ~ Thorough working knowledge of Safety (culture change) and GMP/FDA ~ Experience in Continuous Improvement ~ Production experience Benefits Competitive Salary/ Pay & Packages, Vacations,... 
Suggested
Contract work
Temporary work
Immediate start
Day shift

Tri-Pac Inc

South Bend, IN
19 days ago
 ...collection, including donor set-up, donor monitoring and donor disconnect. •In compliance with SOPs and Food & Drug Administration (FDA) guidelines, performs venipuncture on donors to begin pheresis process. •Evaluates vein performance of the donor to identify... 
Suggested
Part time
Local area

CSL

Terre Haute, IN
1 day ago
 ...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
Full time
Part time
Remote job
Flexible hours

Beckman Coulter Life Sciences

Indianapolis, IN
3 days ago
 ...Under the routine direction of the manager, will be responsible for a variety of complex operations and production duties in an ISO/FDA/QA/EPA/OSHA air separation environment where products include oxygen, nitrogen, argon and hydrogen. Primary Responsibilities... 
Suggested
Holiday work
Local area
Outdoor
Night shift

Praxair, Inc - a Linde Company

East Chicago, IN
9 hours ago
 ...in all safety initiatives * Implements safety and sanitation schedules that ensure the sites compliance with corporate, DOT, OSHA, FDA, AIB or ASI standards. * Performs safety observations to coach employees on safety procedures * Prevents associate incident and injury... 
Suggested
Holiday work
Full time
For contractors
Local area
Night shift

NFI Industries, Inc.

Indiana
1 day ago
 ...documentation (e.g. P&ID’s, URS, FS, DS). Knowledge of Data Historian (OSIPI) Knowledge of Computer System Validation lifecycle and FDA regulatory requirements. Desired Soft Skills: Excellent analytical and problem-solving skills to be applied in troubleshooting... 
Suggested

PACIV

Indianapolis, IN
2 days ago
 ...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

Kimball Electronics

Indianapolis, IN
4 hours agonew
 ...training.Operation Excellence Maintains Commercial Pesticide License, and Pesticide Business Licensing Ensure that facility complies with FDA requirements, as well as GMPs, SOPs, and other standards through facility inspections. Provide management with results/... 
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For contractors
For subcontractor
Local area

Compass Group

Mount Vernon, IN
7 hours agonew
 ...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

Trane Technologies

Noblesville, IN
9 hours ago
 ...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... 
Temporary work
H1b
Weekend work
Day shift

Eli Lilly and Company

Indianapolis, IN
3 days ago
 ...Ensures compliance with all applicable local, state, and federal regulatory requirements which include but are not limited to: FDA, OSHA, EPA, ISO, and DOT Establishes and maintains relationships with suppliers, contractors, and OEMs to ensure plant is adequately... 
Holiday work
Contract work
Temporary work
For contractors
Local area
Night shift

Praxair, Inc - a Linde Company

Chesterton, IN
1 day ago
 ...to standard. Ability to manage staff training and supervision and knowledge of Good Manufacturing Procedures (cGMP) guidelines, and FDA regulations are essential for this position. JOB DUTIES AND RESPONSIBILITIES Production Manager's responsibilities will include, but... 
Gangs

ResourceMFG

Princeton, IN
4 days ago
 ...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... 
Work from home
Shift work

Trane Technologies

Noblesville, IN
3 days ago
 ...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... 
Contract work
Temporary work
Local area
Shift work
Night shift
Day shift
Afternoon shift
All shifts

Kimball Electronics

Indianapolis, IN
1 day ago