Demo

Calibration Technician or Test Technician

SEDAA
BURLINGTON, MA Full Time
POSTED ON 1/13/2026
AVAILABLE BEFORE 3/13/2026

*******LOCAL CANDIDATE ONLY OR OPEN TO RELOCATE TO BURLINGTON,MA  ****NO C2C CANDIDATES*************

Requisition Title: Test Engineer/Technician 

Location: Burlington, MN (Onsite)

JP# Sedaa 43752

Pay Rate : 50k/Ann- 70k/Ann 

MAIN PURPOSE OF ROLE

  • Perform failure analysis on explanted biomedical implant product. Provide technical expertise to the Product Analysis Laboratory. Analyzes failures, develops, and implements investigative protocols to identify root causes, performs circuit analysis, performs device and component level failure analysis.

Main Responsibilities

  • Perform failure analysis on explanted long-term biomedical implant product.
  • Work requires the application of theoretical principals, evaluation, ingenuity, and creative/analytical techniques to identify route cause failure mechanisms.
  •  Must be able to meet deadlines on multiple assignments and be able to operate in a diverse cross-functional team environment.
  • Proactive in finding quality improvements related to Failure Analysis
  • May serve as lead and assign work to less experienced personnel and serves as a mentor when assisting less experienced lab staff in solving more complex problems.
  • Works cross functionally and collaboratively with Product Development, Engineering, Manufacturing, and Product Surveillance.
  • Aides in definition of test equipment as required to accomplish quality responsibilities.
  • Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
  • Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
  • Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.

Education

Qualifications

  • Bachelor’s Degree in Engineering is Required
  • Electrical or Biomedical Engineering is preferred
  • Engineering work experience is preferred
  • Knowledge of global regulations for medical device reporting and medical terminology is a positive
  • Strong written and oral communication skills are required
  • Candidate must be able to work well independently and on teams in a busy department while managing multiple ongoing tasks and investigations simultaneously
  • Multitasks, prioritizes, and meets deadlines in a timely manner
  • Strong organizational and follow-up skills, as well as attention to detail


*******LOCAL CANDIDATE ONLY OR OPEN TO RELOCATE TO BURLINGTON,MA  ****NO C2C CANDIDATES*************

Requisition Title: Test Engineer/Technician 

Location: Burlington, MN (Onsite)

JP# Sedaa 42761

Pay Rate : 50k/Ann- 68k/Ann 

Description: Engineer-Degreed 1

This is an entry level onsite position for the Burlington location. Selected candidate will start ASAP after screenings have cleared.

Top 3 Skills or Any Specific type of Experience you are looking for:

  1.  Must have great collaboration skills
  2. Must be able to work in a fast-paced and evolving environment
  3. Must be a self-starter/go-getter
  • Must work well within a team environment and have good collaboration skills.
  • Willing to jump in and be a self-starter and able to learn and grow among the team.

Technical skills include:

  • Requirements creation/management
  • Verification protocol/report writing
  • Test Execution
  • Ability set and work with lab equipment
  • Create dFMEA’s
  • Create Systems Architecture
  • Possesses educational qualifications and work experience as established by engineering schools, employers and licensing authorities for employment in the various disciplines of engineering, i.e. Systems, Mechanical, Electrical, Industrial, Chemical.
  • Entry level to 0 - 3 yrs. experience needed.

This position includes:

  • General Systems Engineering activities (i.e. requirements development/management, MBSE, Risks, V&V)
  • Lab setup/maintenance

Role is to be performed Onsite.

  • Support of Systems Engineering Team Deliverables


*******LOCAL CANDIDATE ONLY OR OPEN TO RELOCATE TO TEXAS ****NO C2C CANDIDATES*************

Requisition Title: Calibration Technician / Instrumentation Technician
Location: Plano, TX (Onsite)

JP# Sedaa43216

Pay Rate : 20k/Ann- 27k/Ann 

Description:

Duties: Performing beginning calibration activities. Basic mechanical, pressure equipment verification to support internal customers. Potential to run some automated system calibrations. Working in the calibration lab, some data entry duties

Experience: 1-2 years’ of experience; Testing of equipment, Lab experience is plus, Test Tech of equipment, analysis work, scientific notation, unit conversions (measurements)

Key Skills: Computer experience with excel. Read and follow written instructions. Inquisitive and eager to learn. Attention to detail. Ability to work as a team member.

Preferred Experience: Some experience working with testing, quality, Knowledge of Multimeters, Calipers is a plus

Education: HS diploma or equivalent work experience in a related field (Master degree may be over qualified) Associate degree will be considered with experience.


*******LOCAL CANDIDATE ONLY OR OPEN TO RELOCATE TO IRVING, TX ****NO C2C CANDIDATES*************

Requisition Title: Test Technician

Location: : Irving, TX (Onsite)

JP# Sedaa 43226

Pay Rate : 31k/Ann- 34k/Ann 

Description:

Job Summary:

Description:

Description:

Job Summary:

Working under general supervision, this position is responsible for the production of high-quality medical device instruments. This position includes detailed assembly and testing of various electronic components and finished devices in a controlled manufacturing environment.

Job Responsibilities:

• Performs testing of electronic components and assemblies using automated test equipment

• May perform mechanical assembly of electromechanical subassemblies and devices

• Ability to read, comprehend and follow written procedures; understand and follow verbal instructions. May instruct others in the use of all manuals, test procedures and documentation associated with specialized equipment.

• Reads and interprets engineering drawings, schematics and complex test procedures.

• Participates in continuous improvement/quality initiatives in order to enhance production processes to achieve quality and profitability metrics.

• Maintains accurate records to ensure Device History Records and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products.

• Prioritizes work by determining the sequencing and timing of different jobs based on precedence and importance.

• Positively represents the company during tours by demonstrating techniques and sharing appropriate information.

• Supports all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.

• Complies with U.S. Food and Drug Administration (FDA) regulations, ISO or other regulatory requirements, Company policies, operating procedures, processes, and task assignments.

• Adheres to all environmental, health and safety SOP’s, equipment, policies and procedures, including any department specific requirements.

• Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.

Minimum Qualifications:

• Experience with electronic assembly and test in a medical device industry preferred.

• High School Diploma or equivalency is required, preferred AAS

• 2 or more years experience with electromechanical assemblies/electronic manufacturing, technical certifications, etc. preferred

Preferred Qualifications:

• Experience in troubleshooting equipment, building and or testing of electronic assemblies

• Working knowledge of IPC standards and use of complex tools and equipment specific to functional areas

• Experience in GMP, ISO, and FDA controlled environments preferred

• Ability to work within a team and as an individual contributor in a fast-paced, changing environment.

• Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.

• Multitasks, prioritizes and meets deadlines in timely manner.

• Strong organizational and follow-up skills, as well as attention to detail.

• Ability to maintain regular and predictable attendance.

• Ability to work scheduled overtime as required is preferred.

• Ability to hand and lift up to 25 lbs. as needed for specific job functions

• Must be able to sit and/or stand for long periods of time.

• Ability to frequently sit, stand, walk, reach within hands and arm’s length, stoop, kneel and crouch.


Salary : $50,000 - $68,000

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