Akkodis is seeking a Quality Assurance Technician for a Contract job with a client in Germantown, MD . The ideal candidate must have experience working in a regulated manufacturing environment, preferably within the medical device industry, along with strong knowledge of quality systems, inspections, and compliance requirements.

Rate Range:

$32/hour to $35/hour ; The rate may be negotiable based on experience, education, geographic location, and other factors. Quality Assurance Technician job responsibilities include: Perform quality control inspections of medical devices in accordance with approved procedures, specifications, and SOPs. Conduct incoming, in-process, and final product inspections to ensure compliance with quality standards and engineering requirements. Complete inspection reports, nonconformance documentation, and quality records accurately and timely. Review Device History Records (DHRs) for completeness, accuracy, and regulatory compliance. Collaborate with Purchasing, Operations, and Quality teams to manage nonconforming materials and ensure proper material disposition. Support document control processes, technical documentation maintenance, and Device Master Record (DMR) management. Support calibration programs, equipment records, and associated documentation. Assist with Supplier Corrective Action Requests (SCARs), CAPAs, and quality improvement initiatives.

Desired Qualifications:

High School Diploma or GED required; Bachelor's Degree preferred . Minimum 3 years of experience in a quality role within a medical device company or other regulated manufacturing environment. Experience working with Quality Management Systems (ISO 9001, ISO 13485, or similar regulated standards) .

Proficiency using inspection equipment including:

Calipers, Micrometers, Plug Gages, Thread Gages Experience using and programming Keyence Vision Systems .

Proficiency with:

Microsoft Word, Excel, Outlook, eQMS Systems, ERP Systems. Ability to read and interpret engineering drawings, blueprints, and schematics.

Knowledge of:

CAPA Processes, Audits, Good Documentation Practices (GDP), Line Clearance.

Preferred Qualifications:

Medical device industry experience.

Professional quality certifications such as:

CQE (Certified Quality Engineer) CRE (Certified Reliability Engineer) Six Sigma Certification Other Quality Certifications Experience supporting FDA-regulated manufacturing environments. If you are interested in this role, then please click

APPLY NOW.

For other opportunities available at Akkodis, or any questions, feel free to contact me at Sunny.

Kumar1@ akkodisgroup.com .

Pay Details:

$32.00 to $35.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to https://www.akkodis.com/en/us/candidate-privacy-policy The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: The California Fair Chance Act Los Angeles City Fair Chance Ordinance Los Angeles County Fair Chance Ordinance for

Employers San Francisco Fair Chance Ordinance Massachusetts Candidates Only:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.