Associate Engineer

Reposted 4 Days Ago
Be an Early Applicant
Savannah, GA, USA
In-Office
Mid level
Healthtech
The Role
Support design and manufacturing of dental and medical devices: develop processes, create documentation (DHF/DMR), perform validations (IQ/OQ/PQ), support NPI, build software/controls, and ensure GMP/regulatory compliance.
Summary Generated by Built In
Don’t just work somewhere, join Brasseler and be a valued team member of a world-class health care organization!

Our Culture:
Provides a safe and welcoming environment where team members can balance their lives and develop their careers. All people and experiences are valued and respected. Different perspectives are encouraged and lead to better results. This makes us who we are and enables us to be a world-class healthcare organization. All who join us are accountable to this charge.

Our Philosophy:

Quality products sold with integrity has been the hallmark of Brasseler USA from the beginning. Brasseler USA’s strong reputation of providing high quality, clinician endorsed and innovative dental and medical instrumentation nationally has spanned over 40 years. We have been offering a full-range of products made in the USA since 1976. Many of our products are manufactured at our headquarters in Savannah, GA.

Explore our career opportunities below to learn more.

JOB OVERVIEW: 

 

This role will be responsible for providing engineering skills to support product and process development in dental and medical fields. The Associate will learn and apply the latest standards and best practices in process, design, and validation of health care products. Responsibilities include developing creative solutions in areas of product design, develop and characterize new robust manufacturing processes and develop a deep understanding of the latest GMP and regulatory requirements. Must be able to execute on project deliverables to meet project and site goals.  

 

KEY RESPONSIBILITIES:   

General 

 

  • Provide key engineering functions on one or more teams 

  • Present deliverables to team leaders 

  • Own deliverables within larger projects 

  • Learn the intended use and functional requirements of dental and medical devices 

 

Process 

  • Provide manufacturing engineering support for production and assembly operations.  

  • Develop an understanding of key performance indicators (KPIs) that influence processes. 

  • Participate in reviews of process design for compliance with engineering principles, company standards, customer contract requirements, and related specifications. 

  • Analyze equipment to establish operating data, conduct experimental tests and evaluate the results 

  • Prepare the production "package" including work instructions, travelers, drawings, labeling, etc. 

  • Complete equipment and process validations (IQ, OQ, PQ). 

  • Learn/master common components and equipment as well as specifications, reliability requirements, and regulatory requirements 

  • Assist and learn in initiatives for the development, introduction, improvement and sustainment of manufacturing processes.  

 

Design/Development 

  • Use engineering training in the design, development, testing, documentation and manufacturing of products with adherence to industry & GMP standards 

  • Contribute to design history file (DHF) creation including design review meetings, phase signoffs, and final transitions to manufacturing. 

  • Learn and support the design control process (DMR, DHF, Technical Files, etc.)  

  • Create drawings, documentation, and specification for products as well as maintenance of documentation for existing products. 

  • Assist with design models, drawing details, assembly drawings, and associated engineering documentation with 3-D parametric modeling software, MS Word, EXCEL and MS Power Point. 

  • Assist and learn in continuous improvement activities focused on current product performance and costs. 

  • Support final product verification and validation. 

  • Update documentation for existing products. 

  • Update work instructions, travelers, drawings, labeling, etc. based on guidance from senior staff regarding changing regulatory requirements. 

  • Learn and supports the new product introduction process from conceptualization through introduction to manufacturing. 

  • Learn and supports the new product development process. 

  • Work to learn/master new product introduction (NPI) requirements 

  • Learn and provide support in voice of customer (VOC) surveys. 

  • Carry out testing of new products to evaluate performance and provide data for improvements/innovation. 

  • Work to learn/master sterilization, material characterization, cleaning validations, metrology, and inspection techniques. 

  • Work to learn/master industry standards and local regulations pertaining to the environment, health, and safety. 

 

Software 

  • Develop software and controls for manufacturing applications. 

  • Support/learns about translating physical manufacturing workflow requirements to software requirements. 

  • Design, develop, debug, maintain, and document software components. Support/learn about software and formatting across multiple applications and processes throughout the site. 

  • Provide software support for SLA, 3D Printing, CNC Milling, Laser Marking and Laser Trimming, X-Ray Tomography, and manufacturing systems integration with commercial software system ERP, MES and data warehousing systems. 

  • Support/learn User Acceptance Testing scenarios and protocols. 

  • Complete process validations (IQ, OQ, PQ) within Operations to 21 CFR Part 11 compliance. 

  • Support/learn development and implementation of Application Programming Interfaces (APIs) 

  • Support/learn integration of multiple components from various sources into software applications. 

  • Support/learn drafting of high-level technical architecture. 

 

Electro/Mechanical 

  • Support the design and assembly of devices and equipment that blend electrical and mechanical components.  

  • Support the development of equipment and devices at all stages, from concept creation to production tooling. 

  • Aim to optimize safety, economy, reliability, sustainability, and quality. 

  • Design equipment tooling to improve machine and process efficiency. 

  • Perform maintenance on process equipment. 

  • Learn/master the equipment and control systems utilized in the assigned manufacturing area. 

  • Generate accurate and controlled documents pertaining to process equipment. 

 

SPECIFIC KNOWLEDGE & SKILLS:   

 

  • Bachelor’s or Masters Degree in Engineering (Mechanical, Chemical, Physics, Computer sciences) 

  • Ability to read and interpret documents such as operating and maintenance instructions, technical drawings, industrial standards and procedure manuals  

  • Ability to write routine and technical reports and correspondence. 

  • Detail oriented, and ability to organize, document and communicate across the organization.  

  • Proficient in MS Word, Excel, Outlook, and MS Power Point 

 

GENERAL SKILLS & COMPETENCIES:   

  •  Basic understanding of industry practices 

  • General proficiency with tools, systems, and procedures 

  • Basic planning/organizational skills and techniques 

  • Good decision making, analysis and problem solving skills 

  • Good verbal and written communication skills 

  • Basic presentation and public speaking skills 

  • Basic interpersonal skills 

  • Developing professional credibility 

 

MINIMUM WORK EXPERIENCE:   

 Typically 2 to 4 years of related professional experience. 

 

PREFERRED EDUCATION:   

 Typically a Bachelor's Degree or global equivalent in related discipline. 

 

TRAVEL / PHYSICAL DEMANDS: 

 Travel typically less than 10%. Office environment. No special physical demands required. 

 

Benefits available include: Medical, Dental and Vision Coverage, 401K Plan with Company Match, Generous Time Off, Paid Parental Leave, Income Protection, Work Life Assistance Program, Flexible Spending Accounts, Educational Benefits, Worldwide Scholarship Program and Volunteer Opportunities.

*Benefits may vary by location or status.

Henry Schein is an Equal Employment Opportunity Employer and does not discriminate against applicants or employees on the basis of race, color, religion, creed, national origin, ancestry, disability that can be reasonably accommodated without undue hardship, sex, sexual orientation, gender identity, age, citizenship, marital or veteran status, or any other legally protected status.

Fraud Alert

Henry Schein has recently been made aware of multiple scams where unauthorized individuals are using Henry Schein's name and logo to solicit potential job seekers for employment.

Please be advised that Henry Schein's official U.S. website is www.henryschein.com. Any other format is not genuine. Any jobs posted by Henry Schein or its recruiters on the internet may be accessed through Henry Schein's on-line "career opportunities" portal through this official website. Applicants who wish to seek employment with Henry Schein are advised to verify the job posting through this portal.

No money transfers, payments of any kind, or credit card numbers, will EVER be requested from applicants by Henry Schein or any recruiters on its behalf, at any point in the recruitment process.

Skills Required

  • Bachelor's or Master's Degree in Engineering (Mechanical, Chemical, Physics, Computer Sciences)
  • Typically 2 to 4 years of related professional experience
  • Proficient in MS Word, Excel, Outlook, and PowerPoint
  • Experience with 3-D parametric modeling software and creating design/drawing documentation
  • Knowledge of GMP, medical device regulatory requirements, and 21 CFR Part 11 compliance
  • Ability to perform equipment and process validations (IQ, OQ, PQ)
  • Familiarity with manufacturing equipment and processes (SLA/3D printing, CNC milling, laser marking/trimming, X-ray tomography)
  • Ability to read technical drawings, write technical reports, and produce work instructions/travelers

Henry Schein Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Henry Schein and has not been reviewed or approved by Henry Schein.

  • Healthcare Strength Health, dental, and vision coverage is broadly comprehensive, with multiple plan options and wellbeing/EAP resources emphasized. Benefits breadth helps bolster overall total‑rewards value.
  • Leave & Time Off Breadth Paid time off and holidays are described as meaningful, with structured carryover practices in some areas. Paid parental leave is available, enhancing the overall time‑off offering.
  • Retirement Support A 401(k) plan with company match is part of the standard package, with plan documents noting employer discretion on match settings. The program has been characterized positively in prior periods, contributing to total compensation.

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The Company
HQ: Melville, NY
8,580 Employees
Year Founded: 1932

What We Do

Henry Schein, Inc. (Nasdaq: HSIC) is a solutions company for health care professionals powered by a network of people and technology. With more than 20,000 Team Schein Members worldwide, the Company's network of trusted advisors provides more than 1 million customers globally with more than 300 valued solutions that help improve operational success and clinical outcomes. Our Business, Clinical, Technology, and Supply Chain solutions help office-based dental and medical practitioners work more efficiently so they can provide quality care more effectively. These solutions also support dental and medical laboratories, government and institutional healthcare clinics, as well as other alternate care sites.

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