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Manufacturing Engineer II

Argen Corporation
Posted a day ago, valid for 19 days
Location

San Diego, CA, US

Salary

$105,000 per year

Contract type

Full Time

Wellness Program

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Sonic Summary

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  • Argen Corporation is seeking a Manufacturing Engineer II to join their technology-focused team in San Diego, CA, offering a salary of $80,000 to $90,000 per year.
  • Candidates should possess a B.S. degree in engineering or a related field, along with a minimum of 3 years of relevant experience.
  • The role involves overseeing process development, equipment design, and ensuring compliance with FDA and ISO regulations.
  • Successful applicants will demonstrate strong communication skills and knowledge of process validations in a medical device manufacturing environment.
  • Argen offers a comprehensive benefits package, including health plans, a 401k with employer match, and various employee discounts.
 

Manufacturing Engineer II

Argen Corporation currently has an exciting opportunity for a Manufacturing Engineer II to join a growing, technology-focused and service-oriented team.  Do you thrive in a fast- paced and dynamic environment? If you would like to be a part of an organization with an unwavering commitment to quality dental solutions, then explore our career opportunities and get to know Argen. 

About Us
Argen is a family-owned and privately held company based in San Diego, CA with a state-of-the-art manufacturing center that provides high quality dental solutions to dental labs of all sizes. Founded as a precious metals company in South Africa, Argen has evolved into a dynamic, technology-based manufacturing organization focused on three key business segments, including dental alloys, zirconia, and digital dentistry solutions. Argen continues to invest in innovative product improvement initiatives through its Quality Management System to provide our global customers with affordable, high-performance products and industry-leading excellent service. Argen’s products are FDA regulated and ISO certified.

In this role, the successful candidate will be:
• Responsible for overseeing and reviewing process development, equipment/tooling design, process characterization, process validation, inspection and test development, risk documentation, statistical analysis, production documentation. Drive product product/process/yield improvement activities in partnership with other functional areas such as Manufacturing, Research & Development, Facilities, and Quality departments. Prepares and/or reviews all protocols and reports involving validation tasks.
• Resolve manufacturing issues that require an engineering solution
• Implements design features and design changes into production by developing new engineering solution and updating manufacturing documentation
• Executes design verifications and process validations including writing protocols and test reports
• Contributes to cross functional teams for completing activities such as Failure Mode & Effects Analysis (FMEA), process control, or other activities as required
• Completes documentation for all projects to ensure FDA and global compliance with regulatory requirements
• Provides engineering support for manufacturing and quality troubleshooting
• Provides technical expertise and guidance for the preparation and execution of validation protocols and reports.
• Reviews and investigates anomalies.
• Gathers data and performs analysis.
• Resolves and consults on applicable validation compliance and manufacturing process issues.
• Demonstrates commitment to the development, implementation and effectiveness of Quality Management System per ISO, FDA, and other regulatory agencies.
• Implement new equipment (calibration/set up) and perform training to operation team
• Reviews and develops manufacturing documents (WI, SOP, Forms, etc.).
• Other duties as assigned.

What does it take to be successful?
• B.S. degree or equivalent in engineering or related field.
• 3 years of related experience.
• Strong communication skills.
• Experience preparing and reading technical documentation.
• Working knowledge of standard machine shop equipment and process.
• Knowledge of medical and technical development.
• Ability to use MS Office and other manufacturing systems.
• Knowledge of Process Validations in medical device manufacturing environment.
• Knowledge of cGMP regulations ISO 13485, 21CFR Part 820, CMDR SOR/98-282, 93/42/EEC, RDC 16 2013, MHLW MO 169 and TG(MD)R Sch3 preferred.
• Troubleshooting and problem solving skills.
• Minimum 2 years’ experience in CAD tooling/fixture design (SolidWorks preferred).


Our Awesome Benefits!
Working for a growing innovative company like Argen means exciting opportunities for training and learning, career development and advancement from only the best in the dental industry. With all that hard work, Argen is committed to ensuring the welfare of its employees and provides an amazing benefit package that includes:
• Health/Dental/Vision Plans
• 401k with Employer Match
• Paid Vacation, Holiday and Sick Time
• Employee Events
• Wellness Programs
• Discounts for home, travel, entertainment, relaxation that includes Mobile phone service, Technology, Airline and Hotel, Theater/Theme Park tickets, Restaurants and so much more!

EOE/M/F/Vet/Disabled VEVRAA Federal Contractor




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