Senior Quality Engineer

NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976.

We are shaping the industry. NAMSA has been a key contributor to the development of the test methods that govern our industry. We have become the industry’s premier provider. We provide support for clients during every step of the product development lifecycle and beyond.

Come and work for an organization with the:

to inspire innovative Med Tech solutions that advance global healthcare, improve patient lives and accelerate Client success and the

to deliver best-in‑class global Med Tech development solutions through our people, expertise and technology by adhering to our core

• Act with integrity in everything we do.
• Provide best‑in‑class customer experiences.
• Develop superior talent and deliver expertise.
• Respond with agility and provide timely results.
• Embrace collaboration, diverse perspectives and ideas.

• Experienced with management of equipment procurement process and aids in identifying/developing criteria for procurement/installation of new Measurement and Test Equipment (M&TE) for laboratories with respect to testing standards.
• Design and execute qualifications, requalifications and process validations of M&TE as required by appropriate Biotech and Pharmaceutical industry regulations and standards (e.g., 21 CFR Part 820, ISO 17025, etc.).
• Analyze qualification, requalification and validation raw data and generate final reports.
• Work with IT to ensure equipment that generates electronic data is complaint with 21 CFR Part 11.
• Investigate and troubleshoots using advanced mathematical and engineering knowledge.
• Complete nonconformance, corrective action and preventative action documentation.
• Prepare, review and maintain written technical documents for M&TE, including protocols, reports, Standard Operating Procedures (SOPs) and Equipment Operating Procedures (EOPs).
• Perform raw data review for qualifications, calibrations, and equipment service.
• Write and implements change control plans and risk assessments.
• Experienced with coordinating and documenting scheduled/unscheduled maintenance of equipment.
• Experienced and possesses technical aptitude required for requalifying, conducting process validations and trouble‑shooting sterilizers and resistometers.
• Experienced with driving purchasing process for materials/services needed for owning departments.
• Maintain and support equipment documentation in the Equipment Management System.
• Provide training on equipment use to laboratory and support staff.
• Drive trending and analysis of TE failures.
• Experienced with installing, qualifying and maintaining Siemens monitoring points.
• Assists laboratory personnel with continuous monitoring and alarm investigations.
• Administrate and performs maintenance and upgrades of engineering software systems.
• Create and maintain Associate user accounts to all Engineering systems.
• Responsible for writing and executing building expansion validations.
• Updates/Maintains Engineering drawings for buildings, equipment and system.
• Update and maintains Engineering drawings for buildings, equipment and systems.
• Provide equipment records to appropriate staff as needed for client audits and acts as qualification/validation SME where appropriate.
• Train Associates on new and existing equipment and processes.
• Apply standard engineering techniques to improve various processes and assists the laboratories with identifying equipment needs for proactive planning.
• Ensure electronic and paper equipment files are retired/archived appropriately.

• Bachelor degree in engineering or related scientific discipline required.
• 5 to 7 years of related work experience.
• Microsoft Word and Excel experience required.
• Knowledge of regulatory requirements, requirement specifications, systems qualifications and protocols, equipment operating procedures, standard operating procedures, and validation reports.
• Strong written and verbal communication skills.
• Strong…