| Job alert | Jobs 21 - 30 of 449 |
Supervisor, Manufacturing Technical Services
Operations
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Piscataway, NJ
... - Advanced Specialized Knowledge: FDA's validation guidelines & requirements. Demonstrated knowledge and understanding of oral dosage formulation process, manufacturing process and equipment. 21 CFR Statistical analysis. Thorough knowledge of cGMP ... - Jun 13
Food Processing Machine Operator
Paragon Staffing, LLC
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Raritan, NJ, 08869
... experience with food safety and FDA regulations (Required) Understanding of what the machine is for, how it works, and best practices Previous experience with plastics injection molding (Required)SHIFT AVAILABILITY All Shifts Pay Rate: Up to $25/hr. ... - Jun 01
Nurse III
Tellus Solutions
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Branchburg, NJ
... Job Description: Responsibilities: Responsible for maintaining compliance with FDA, AATB, international and state regulations during the second level quality review of all tissue donor files for tissue submitted to Allergan to ensure the safety of ... - Jun 17
Senior Validation Manager
Catapult
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Princeton, NJ
... In this role, you will define, implement and maintain the validation program for the site, ensuring compliance to the company quality guideline, FDA regulatory requirements, and cGMP regulations. RESPONSIBILITIES The ideal candidate will have strong ... - Jun 08
Manufacturing Operator
Caresoft Inc.
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Raritan, NJ, 08869
... Carry out duties in compliance with all state and federal regulations and guidelines including FDA, TUV, EPA and OSHA. Adhere to the safety code of Conduct & EHS policies and attend all required EHS training. Follow Global Leadership Profile (GLP) ... - Jun 12
Labeling Specialist
Bausch Health
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North Branch Depot, NJ, 08869
... KEY ACTIVITIES/RESPONSIBILITIES Provide Regulatory support in the development, revision, review, and approval of labeling content for submission to FDA, as well as any post marketing labeling changes. Assist Labeling Leads with proofreading of ... - May 31
Documentation Specialist
Joulé
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Trenton, NJ
Title: Document Specialist Location: Cranbury, NJ Schedule: M-F Full Time Type: Direct Hire Responsibilities The Document Specialist is responsible for maintaining all production and quality related documents according to the SQF & FDA requirements. ... - Jun 09
Pharmaceutical Equipment Commissioning & Qualification Engineer
Piper Companies
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Titusville, NJ, 08560
... and validation Experience with lab equipment commissioning and decommissioning, HPLC, UPLC, and CSV Knowledge of FDA and EU cGMP regulations, ICH guidelines, GALP, GLP, GDP, and other industry best practices Bachelor's or higher degree in ... - Jun 17
Registered Nurse
Planet Pharma
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Branchburg, NJ
... JOB SUMMARY: Responsible for maintaining compliance with FDA, AATB, international and state regulations during the second level quality review of all tissue donor files for tissue submitted to Allergan to ensure the safety of donated human tissue. ... - Jun 18
Materials Management Supervisor, Onsite
AbbVie
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North Branch Depot, NJ, 08876
... Coordinate training and ensure 100% training compliance in an FDA-regulated environment. Prepare, compile, and review documentation for production processing for completeness and accuracy. Develop, write, review, and update Standard Operating ... - Jun 05