Associate Chemical Engineer, Sustaining R&D

Kerr Dental

Pomona (CA)

On-site

USD 70,400 - 80,000

Full time

14 days+

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Benefits offered by this job

Annual performance bonus
Medical/dental/vision benefits
401K match

Job summary

Metrex is seeking a Sustaining R&D Associate Chemical Engineer to drive design improvements and testing for currently marketed products. You will verify, validate, and implement changes while coordinating with quality, manufacturing, and other functions to enhance performance and cost-efficiency.

The role involves creating verification/validation reports, reviewing change requests, and contributing to risk management.

Qualifications

  • Bachelor's in Engineering, Chemical Engineering preferred.
  • Relevant engineering experience is required.
  • Must reside within commuting distance to Pomona, CA; this is not remote.

Responsibilities

  • Support R&D Sustaining Engineering initiatives under general supervision.
  • Collaborate with project teams to assess, verify, validate and implement product design changes.
  • Create and conduct design verifications, validation protocols and reports.
  • Review design change requests to support manufacturing, packaging and labeling changes.
  • Provide input on Risk Management activities and participate in GLP-related tasks.
  • Perform product testing, evaluation, failure analysis and investigation of customer returns.
  • Interface with suppliers and factories regarding product technical issues when required.
  • Prepare cost estimates for proposed major design products.
  • Travel up to 5% as needed.

Skills

Chemical engineering
Cross-functional collaboration
Excellent communication

Education

Bachelor's in Engineering (Chemical Engineering preferred)

Tools

SolidWorks
AutoCAD

Job description

Position Overview

The Sustaining R&D Associate Chemical Engineer is involved in design, product improvement, testing and analysis utilizing a variety of chemical engineering disciplines. As a member of the Sustaining R&D team, you will verify, validate, and implement design changes to currently marketed products. This role supports cross-functional initiatives, including product development, quality, manufacturing, customer service, sales, marketing, and procurement, to enhance product performance, quality, customer satisfaction, and cost-efficiency, while ensuring compliance with internal quality systems and applicable EPA & FDA regulations in the consumable medical device and antimicrobial pesticide industry.

  • Supports all initiatives related to R&D Sustaining Engineering under very general supervision.
  • Collaborate with project team members and other functional departments to assess, verify, validate and implement product design changes to currently marketed products in alignment with internal design change procedures.
  • Create and conduct design verifications, validation protocol and reports.
  • Review and evaluate design change requests to products to support changes in manufacturing processes, packaging, and labeling.
  • Provide input on Risk Management activities as per company procedures.
  • Perform product testing, evaluation, failure analysis and investigation of customer returns.
  • When required, interact with our Suppliers and factory regarding product technical issues.
  • Create and/or modify product design, specifications, drawings, procedures, CAD models (Solidworks/ AutoCAD) and Engineering Change Requests in accordance with quality system procedures.
  • Collect and provide product design feedback to engineering and production operations personnel.
  • Investigate customer complaints and field failures, develop solution and implement the solution into production in accordance with internal quality system procedures. This will require interfacing with our Customer Care Team and sometimes our customers.
  • Prepare cost estimates on proposed major design products.
  • Estimate 5% travel will be required for this position.
Required
  • Bachelor's in Engineering, Chemical Engineering degree is preferred
  • Relevant Engineering experience
  • Must reside within a commutable distance to Pomona, CA. This is not a remote or hybrid role.
Preferred Skills
  • Experience with dental devices is optional but desirable.
  • Experience with standard chemical/physical testing and/or engineering development/optimization.
  • Experience with analytical instruments (pH meter, densometer, gas chromatography, and auto-titrator) is desirable.
  • Basic understanding of root-cause analysis.
  • Performed lab duties under good laboratory practices (GLP).
  • Experience in wet chemistry and liquid formulation techniques.
  • Basic understanding of FDA QMSR Part 820 and ISO 13485.
  • Excellent oral and written communication skills
Target Market Salary Range

Actual compensation packages take into account a wide range of factors that are unique to each candidate, including but not limited to geographic location; skill sets; relevant education and certifications; depth of experience; performance; and other business and organizational needs. The disclosed reasonable estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Envista, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. The total compensation package for this position may also include an annual performance bonus, medical/dental/vision benefits, 401K match, and/or other applicable compensation plans.

$70,400 - $80,000

Operating Company

Metrex

Envista and all Envista Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available at: http://www.dol.gov/ofccp/regs/ compliance/posters/pdf/eeopost.pdf.

Envista and its family of companies (Envista) will not accept unsolicited resumes from any source other than directly from a candidate. Envista will consider unsolicited referrals and/or resumes submitted by vendors such as search firms, staffing agencies, professional recruiters, fee-based referral services and recruiting agencies (Agency) to have been referred by the Agency free of charge and Envista will not pay a fee for any placement resulting from the receipt such unsolicited resumes. An Agency must obtain advance written approval from Envista's internal Talent Acquisition or Human Resources team to submit resumes, and then only in conjunction with a valid fully-executed contract approved by the Global Talent Acquisition leader and in response to a specific job opening. Envista will not pay a fee to any Agency that does not have such agreement and written approval in place.

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