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Quality Control Senior Specialist

Roman Health Pharmacy LLC

Please Note: To conform with the United States Government Space Technology Export Regulations, the applicant must be a U.S. citizen, lawful permanent resident of the U.S., conditional resident, asylee or refugee (protected individuals as defined by 8 U.S.C. 1324b(a)(3)), or eligible to obtain the required authorizations from the U.S. Department of State. At CesiumAstro , we are developers and pioneers of out-of-the-box communication systems for satellites, UAVs, launch vehicles, and other space and airborne platforms. We take pride in our dynamic and cross-functional work environment, which allows us to learn, develop, and engage across our organization. If you are looking for hands‑on, interactive, and autonomous work, CesiumAstro is the place for you. We are actively seeking passionate, collaborative, energetic, and forward‑thinking individuals to join our team. We are looking to add a Quality Control Senior Specialist to our team. In this position, you will work closely on an integrated team of CesiumAstro managers, engineers, and other cross‑functional personnel. You will be responsible for programming and using inspection/analysis equipment, handling nonconformances and corrective actions, calibration and metrology of equipment, as well as performing inspections on electronic assemblies and finished high‑reliability products in compliance with CesiumAstro Quality Management System, international standards, and regulatory requirements.

JOB DUTIES AND RESPONSIBILITIES

Quality Control & Inspection Execute quality control processes per purchased product, manufacturing operations, and customer quality requirements. Inspect parts, assemblies, and finished products utilizing necessary tools and equipment in accordance with approved procedures, specifications, and drawings. Perform measurements using calipers, height gauges, thread gauges, and CMM/VMM equipment. Document inspection activities using electronic systems, written logs, and labels. Assist with the control and disposition of non‑conforming material (MRB). Drive scheduling of day‑to‑day quality activities and ensure timely and accurate turnaround of inspection and quality processes. Metrology & Quality Systems Program, maintain, and utilize automated inspection equipment such as CMMs, inspection arms, XRF systems, X‑Ray equipment, and automated visual inspection systems. Perform calibration of equipment and tools used in Quality, Production, and Test activities. Create, document, and update quality processes related to inspection, measurement system analysis (MSA), calibration, and data analysis. Assist in the development, maintenance, and continuous improvement of inspection methods, inspection plans, internal quality procedures, and quality processes. Corrective Action & Continuous Improvement Drive resolution of internal and external nonconformances utilizing root cause analysis, corrective action, and 8D methodologies. Lead cross‑functional teams to identify issues, implement corrective actions, and drive continuous improvement efforts. Conduct data analysis and department metrics reporting to support quality objectives and operational decision‑making. Assist in the resolution of audit findings, observations, and recommendations resulting from internal, customer, and regulatory audits. Perform other quality control duties and special projects as assigned.

JOB REQUIREMENTS AND MINIMUM QUALIFICATIONS

5‑7 years of experience in manufacturing quality, metrology, and failure analysis. Associate degree in a technical field preferred. High school diploma or equivalent. Experience in the aerospace, electronics, or defense industry. Experience with Coordinate Measuring Machines (CMM), metrology arms, Keyence systems, or similar inspection and measurement equipment. Experience with calibration systems and metrology practices preferred. Experience with AS9100 or ISO 9001 Quality Management Systems. Proficiency reading engineering drawings, CAD models, GD&T, specifications, and detailed work instructions. Experience with microscopic visual inspection. Strong attention to detail and ability to follow procedures, specifications, and work instructions. Strong analytical, written, verbal, and digital communication skills. Strong interpersonal skills and ability to work collaboratively with cross‑functional teams.

PREFERRED EXPERIENCE

Experience in regulated manufacturing environments such as aerospace, defense, automotive, or medical device industries. J-STD-001, IPC‑A‑610, and/or IPC/WHMA‑A‑620 certification. CesiumAstro considers several factors when extending an offer, including but not limited to, the role and associated responsibilities, a candidate’s work experience, education/training, and key skills. Full‑time employment offers include company stock options and a generous benefits package including health, dental, vision, HSA, FSA, life, disability and retirement plans. CesiumAstro is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. Please note: CesiumAstro does not accept unsolicited resumes from contract agencies or search firms. Any unsolicited resumes submitted to our website or to CesiumAstro team members will be considered property of CesiumAstro, and we will not be obligated to pay any referral fees. #J-18808-Ljbffr Roman Health Pharmacy LLC

Vacancy posted 2 days ago
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