Job Description
Job Description:
Post Market Quality Technician
Shift Start Time between 6 - 8 am EST
The Post Market Quality Technician plays an integral role in *** s Quality Department as a hands-on engineering role conducting post market investigations of FDA approved medical devices. The position requires strong organization skills, attention to detail, ability to work in cross functional teams, and drive to accomplish departmental and company goals.
Responsibilities:
Perform moderately complex tasks to ensure compliance with quality standards
Partner with quality assurance engineers and other team members to ensure effective inspection and testing procedures are implemented and maintained
Generate, review and maintain Quality records in support of the Quality System, e.G., training, internal audits, Client, and CAPA
Perform product testing and failure analysis
Review Lot Acceptance records and DHRs
Collect log quality data and trend results
Accountability for quality data entry and productivity
Assist in gathering information during FDA and ISO 13485 inspections
Trouble shoot new failure modes.
Evaluate process and engineering controls to improve safety and efficiency.
Perform other duties as assigned.
Education and Experience:
Minimum Requirements:
Associates Degree in an engineering, or scientific discipline
Preferred Skills and Competencies:
Electrical and mechanical background strongly preferred
Prior experience working in a regulated industry (medical device) and/or experience working in a bio-hazard/lab environment preferred
Preferred 2 years in a Quality related function, working with QSR and/or ISO 13485
Computer proficiency in MS office (specifically Excel);experience creating and analyzing charts and Pareto charts a plus
Ability to organize and complete tasks with minimal supervision
Excellent technical writing skills
Excels at generating and maintaining organized and accurate records
Experience with Lean Six Sigma methodology a plus
Physical Requirements (if applicable):
Sitting 70%, Standing 30%
Frequent lifting <5lbs
Occasional (<10% of time) handling (push/pull) up to 50lbs
Ability to operate basic hand tools
NOTE: This position requires on-site working arrangements (requires on-site office/plant/lab work).
Start Date - End Date: Jun 22 Sep 19, 2026
Post Market Quality Technician
Shift Start Time between 6 - 8 am EST
The Post Market Quality Technician plays an integral role in *** s Quality Department as a hands-on engineering role conducting post market investigations of FDA approved medical devices. The position requires strong organization skills, attention to detail, ability to work in cross functional teams, and drive to accomplish departmental and company goals.
Responsibilities:
Perform moderately complex tasks to ensure compliance with quality standards
Partner with quality assurance engineers and other team members to ensure effective inspection and testing procedures are implemented and maintained
Generate, review and maintain Quality records in support of the Quality System, e.G., training, internal audits, Client, and CAPA
Perform product testing and failure analysis
Review Lot Acceptance records and DHRs
Collect log quality data and trend results
Accountability for quality data entry and productivity
Assist in gathering information during FDA and ISO 13485 inspections
Trouble shoot new failure modes.
Evaluate process and engineering controls to improve safety and efficiency.
Perform other duties as assigned.
Education and Experience:
Minimum Requirements:
Associates Degree in an engineering, or scientific discipline
Preferred Skills and Competencies:
Electrical and mechanical background strongly preferred
Prior experience working in a regulated industry (medical device) and/or experience working in a bio-hazard/lab environment preferred
Preferred 2 years in a Quality related function, working with QSR and/or ISO 13485
Computer proficiency in MS office (specifically Excel);experience creating and analyzing charts and Pareto charts a plus
Ability to organize and complete tasks with minimal supervision
Excellent technical writing skills
Excels at generating and maintaining organized and accurate records
Experience with Lean Six Sigma methodology a plus
Physical Requirements (if applicable):
Sitting 70%, Standing 30%
Frequent lifting <5lbs
Occasional (<10% of time) handling (push/pull) up to 50lbs
Ability to operate basic hand tools
NOTE: This position requires on-site working arrangements (requires on-site office/plant/lab work).
Start Date - End Date: Jun 22 Sep 19, 2026
Numbers & Facts
| Location | Acton, MA |
| Industry | Staffing/Employment Agencies |
| Salary | $30 |
| Company Size | 2,000 to 2,499 employees |
| Year Founded | 2000 |
| Website | http://www.lancesoft.com/ |
About Company
We are a $125 Million, NMSDC-certified Minority & Woman owned Workforce Solutions Company headquartered in the DC metro area with presence across US with global presence - Canada, Mexico, India, UK, Malaysia, Indonasia, Hongkong, Singapore, UAE. We are specialized in providing Workforce Solutions, SOW project delivery, Engineering Solutions, Creative Services. We currently support 100+ Fortune companies globally and across multiple industry segments. We are currently supporting several massive programs across industry segment nationally/globally (Intel, Ally, AMD, QUALCOMM, Morgan Stanley, Kraft/ Mondelez, MNP, Amdocs, Dell, SanDisk, Medtronic, Becton Dickinson, GE, Lockheed Martin, UTC, L-3 Communications, Caterpillar, BMW, Mercedes Benz, National Grid, Dominion, Energy Future Holdings, PSEG, 3M, Fidelity, Aetna, Humana, Johnson & Johnson, Pfizer, Merck etc).
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender, identity, national origin, disability, or protected veteran status.