QUALITY ASSURANCE TECH 1 - Litron : Job Details

Litron is seeking a highly motivated QA Tech Level 1 to join our manufacturing team. In this role, you will play a key part in ensuring quality and compliance with industry standards, with a focus on aerospace and medical sectors, including NADCAP. You will work closely with the Quality Manager to maintain quality procedures as dictated by the Quality Management System (QMS). The ideal candidate will have strong attention to detail, a commitment to high-quality standards, and an understanding that the Customer is our first priority. This position is located in Agawam, MA and is Full-time onsite. Responsibilities:• Maintain and update documentation, including standard operating procedures (SOPs), work instructions, and quality manuals.• Ensure accurate organization and storage of documents in electronic and physical formats.• Review existing documents for accuracy and completeness, making necessary revisions.• Assist in developing and implementing document control processes to ensure regulatory compliance.• Collaborate with cross-functional teams to ensure timely and accurate documentation.• Conduct regular audits to ensure documents are current and reflect best practices.• Create reports and presentations summarizing document control metrics and trends.• Perform routine inspections of materials and finished products to ensure compliance with quality standards.• Maintain and update quality control documentation, including test records and inspection reports.• Support the investigation of customer complaints and assist in developing action plans to prevent recurrence.• Provide support during regulatory inspections and customer audits.• Maintain NMR records and logs, and disposition product as directed by management.• Maintain calibration schedule and records.• Manage Customer Feedback Scorecards and generate RMAs as requested by customers and approved by management.• Generate and resolve SCARs/CARs as directed by management.• Perform employee training per QMS requirements.• Maintain the internal audit system per QMS requirements.Requirements• 1-3 years of experience in document control or QA in a manufacturing setting, preferably in aerospace or medical fields.• Familiarity with NADCAP and other regulatory requirements relevant to manufacturing.• Proficient in document control software and Microsoft Office Suite (Word, Excel, Outlook).• Strong attention to detail and organizational skills.• Excellent written and verbal communication skills.• Ability to work effectively in a fast-paced, deadline-driven environment.• Familiarity with ISO 9001 or similar quality management systems.• Ability to collaborate effectively with cross-functional teams.