2203 Engineering jobs in Berkeley Heights,NJ

Bachelor's Degree in Mechanical, Electrical, Industrial, or Chemical Engineering
8+ years of capital engineering project based experience.
Experience managing projects in the $100k -25 Million range
PMP certified or the ability to obtain certification within 12 months of employment.
Experience with technologies including CSD, Juices and Teas, Aseptic, manufacturing equipment including Fillers, Cappers, Conveyance, Packers, Palletizers, Control Systems, RO, and Batch/CIP systems.
Ability to travel for overnight travel +50%
Ability to work independently as a 100% remote employee.

Pye Barker

Union, NJ 07083

Nestle Health Science

Bridgewater, NJ 08807

ADP Technology Services

Roseland, NJ 07068

BrainTrust

New York, NY 10007

Kenvue

Summit, NJ 07901

Bachelor's degree in Plastics/Mechanical/Industrial Engineering or equivalent specialization.
4+ years of experience in Plastics Molding Supplier Quality Management or related field
Expertise in scientific plastics molding (injection, EBM, ISBM, thermoforming), glass forming and process control
Expertise in conducting molding DOE and troubleshooting
Strong knowledge of packaging quality standards
Knowledge of root cause analysis to address plastic molding issues
Ability to travel domestically and internationally up to 25%

electroCore

Rockaway, NJ 07866

Bachelor's degree in Regulatory Affairs, Engineering, Life Sciences, Quality, or a related technical field required
Advanced degree preferred
6-10+ years of progressive medical device regulatory affairs experience preferred
RAC certification, ISO 13485 lead auditor training, MDR/MDSAP training, or comparable regulatory credential strongly preferred
Demonstrated hands-on experience with FDA requirements, 21 CFR Part 820/QMSR transition awareness, ISO 13485:2016, EU MDR 2017/745, UK MDR/UKCA, MDSAP jurisdictions, Health Canada, and TGA expectations
Experience with Class I and Class II medical devices
Experience with software, SaMD, connected devices, or prescription/OTC device labeling is a plus
Proven ability to support or lead regulatory submissions, Technical Documentation maintenance, regulatory change assessments, labeling reviews, PMS/vigilance inputs, and audit support
Experience working in an eQMS/document management system and in cross-functional product development or change control environments
Travel of approximately 20%, including potential support of audits, inspections, supplier visits, regulatory meetings, or trade/business activities