Hologic

Test Engineer 3

Hologic$122K — $203K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 5-8 years of experience in testing and validation for manufacturing environments, particularly in medical devices.
  • Technical Bachelor's degree preferred; advanced degrees are highly regarded.
  • Exceptional knowledge of electro-mechanical equipment, soldering, PCB design, and analog/digital electronics.
  • Prior experience with medical device manufacturing and compliance with FDA regulations.
  • Proficient in MS Office, Solidworks, and programming languages such as C/C++, LabVIEW, and Visual Basic.

Responsibilities

  • Design and develop test and validation methods for test equipment.
  • Create and execute plans, procedures, and protocols for software and hardware testing.
  • Define requirements for test fixtures/equipment and develop corresponding specifications.
  • Diagnose and correct technical issues arising during testing and manufacturing processes.
  • Evaluate testing parameters and analyze defects for process improvement.
  • Collaborate with R&D and Quality teams to ensure system-level test requirements meet design standards.
  • Lead training efforts for assemblers and technicians on new testing equipment and procedures.

Benefits

  • Opportunity for professional development and continued education.
  • Engagement with cross-functional teams including R&D, Quality, and Manufacturing.
  • Involvement in cutting-edge technologies within the manufacturing framework.
  • Mentorship opportunities for the development of Test Engineers and Manufacturing Engineers.
Full Job Description
Job Description

• Designs, develops, and implements test equipment to reliably test and troubleshoot components, sub-assemblies, and systems for manufacturing. Creates test and diagnostic software programs, designs test fixtures/equipment and completes specifications and procedures for new products. The position must ensure that test equipment follows standards for good laboratory practices (GLP) and good manufacturing practices (GMP).
• A seasoned, experienced professional with a full understanding of area of specialization; resolves a wide range of issues in creative ways. This job is a fully qualified, career-oriented, journey-level position. Normally receives little instruction on day-to-day work, general instructions on new assignments.
• Works on problems of diverse scopes where analysis of data requires evaluation of identifiable factors. Demonstrates good judgment in selecting methods and techniques for obtaining solutions. Networks with senior internal and external personnel in own area of expertise.

The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs.
• Owns design and development of test and validation methods for test equipment. Write plans, procedures, and protocols for software/hardware testing activities. (verification and/or validation). Execute verification and/or validation protocols.
• Accountable for defining requirements, developing, and implementing test fixtures/equipment and corresponding specifications and procedures.
• Works with contract manufacturers/vendors to resolve test failures.
• Accountable for identifying, diagnosing, prioritizing, and correcting technical issues that may arise in testing and manufacturing.
• Evaluate and develop testing parameters and outputs for trending analysis. Analyzes defects, provides feedback, and implements process improvements.
• Works with R&D and monitor the system level documentation (HRS, SRS, etc) changes to ensure that system level test requirements meets Design Requirement in manufacturing, including but not limited to EMI compliance, regulatory, safety etc.
• Creates and manages engineering change orders as they relate to test equipment.
• Responsible for developing and leading training of assemblers, technicians and manufacturing engineers on new fixtures, equipment of procedures for production handoff.

What we expect:

Work closely with and contribute to cross functional teams such as R&D (Electrical, Mechanical, System, Software), Quality, Manufacturing and Procurement, Supplier Quality, Other function within the Supply Chain, PMO and Strategic Sourcing.
• Participates in design reviews, working with R&D and manufacturing to create a project test plan for manufacturing, define test requirements, develop test specifications, and define user interface requirements for test equipment as it relates to new product introduction.
• Provide regular communication and updates on success factors such as progress, schedule, budget, project risks and resource or needs gaps.
• Participates in professional development and stays current with new manufacturing test technology and processes while actively seeking to implement new technology into new and existing production lines.
• Collaborates with machine/automation vendors to design, validate, and implement automated equipment/processes.
• Provide mentoring and training for Test Engineers and Manufacturing Engineers.

Education & Experience:

Education

Preferred Minimum Non-Technical Degree: College Degree
• Preferred Minimum Technical/Advanced Degree: Technical Bachelor's Degree

Experience

Preferred Minimum Non-Technical Degree: 5-8 Years
• Preferred Minimum Technical/Advanced Degree: 2-5 Years with Technical Bachelor's Degree, 1-3 Years with master's degree, 0-1 Years with PhD
• Excellent knowledge of electro-mechanical equipment, soldering and PCB design programming and testing, analog and digital electronics, and sensors
• Experienced in supporting medical device manufacturing and applicable government regulations such as FDA, FAA, SEC, etc.

Excellent written and verbal communication skills. Adapts communication style to suite different audiences. Creates precise, accurate technical documentation. Able to facilitate group discussions.
• Strong contributor to high performing team
• Advanced knowledge of MS Office, Solidworks, and programming languages such as C/C++/.net, LabVIEW/CVI, Visual Basic, and/or PLC Ladder Logic
• Working knowledge of manufacturing, quality improvement and cost reduction methodologies such as CIMs, Lean, Root Cause and Root Cause Failure Analysis TQM, SPC and Six Sigma

The annualized base salary range for this salaried role is $122,000 to $203,300 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, geography, education, business needs and market demand.

  • Agency and Third Party Recruiter Notice:
  • Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition, Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms, or they will not be considered.

About Hologic

Hologic, Inc. is an American medical technology company that develops and manufactures diagnostic products, medical imaging systems, and surgical products. The company's products are used in a wide range of medical applications, including breast cancer screening, cervical cancer screening, and osteoporosis diagnosis. Hologic is headquartered in Marlborough, Massachusetts, and has operations in North America, Europe, and Asia. The company was founded in 1985 and has grown to become one of the largest medical technology companies in the world.
Learn more about Hologic
Size
6,705 employees
Market Cap
$18.5 billion
Industry
Net Income
$1.3 billion
Founded
1985
5 Year Trend
+9.7%
Revenue
$4.5 billion
NASDAQ

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