- Legend Biotech USA, Inc. (Raritan, NJ)
- …with alignment to Global Procedures.Act as a Site MES SME to support Quality Investigations, Corrections, and QMS records.Build the Site Readiness of MES ... an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking MES Engineer as part of the Manufacturing Excellence team based in Raritan, NJ. Role… more
- Tris Pharma (Monmouth Junction, NJ)
- …Monmouth Junction, New Jersey, Tris has an immediate opening for a Manager, Quality Management Systems ( QMS ). Summary:The Manager, Quality Management Systems ... ( QMS ) supports, oversees and manages the Quality Assurance (QA) Investigations and Product Quality Complaints Team to ensure manufacturing quality … more
- NESC Staffing (Billerica, MA)
- Quality Engineer Primary Purpose of this Job This position will play a critical role in developing, maintaining, and managing products and processes in ... reviews, and ensuring that the company complies with its Quality Management System ( QMS ). Responsibilities *Maintain and adhere to ISO 9001/AS9100 Quality… more
- Sanofi Group (Framingham, MA)
- **Job Title:** Senior Quality Engineer , QMS **Location** : Framingham, MA **About the Job** We deliver 4.3 billion healthcare solutions to people every year, ... key user of the CAPA, Deviation, and Investigation (CDI) QMS , you'll oversee system health, be the quality... QMS , you'll oversee system health, be the quality approver for records for this system, identify improvement… more
- Actalent (Oil City, PA)
- Job Title: Quality Engineer We are seeking a dedicated and experienced Quality Engineer to ensure compliance with quality management systems and ... for new product introductions. Responsibilities + Ensure compliance with QMS , FDA 21 CFR Part 820, and other relevant...primarily onsite. Additional Skills & Qualifications + CQE (Certified Quality Engineer ) a plus. + Lean Six… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- **Job Description Summary** Develop and sustain quality system processes for the Design Center that complies with applicable regulations and standards, Corporate and ... a **maker of possible** with us. **Responsibilities** + Develop, modify and maintain quality system procedures for the design center that comply with ISO 13485:2016… more
- Actalent (Foster City, CA)
- …Engineer with Medical Device or Combo Device Experience! Description * Act as a quality engineer for medical device QMS quality improvement ... with a focus on design controls and risk management. * Provide oversight of quality improvement activities and ensure compliance with FDA 21 CFR Part 820, 21 CFR… more
- Philips (Cambridge, MA)
- As a Quality Management Systems Software Validation Engineer , you will execute and manage software validation and control activities by authoring, reviewing, ... and subject matter expertise. + Supporting management and standardization of Quality Management System ( QMS ) processes in scope to ensure they are effective and… more
- Philips (Cambridge, MA)
- …in-scope functional & process performance (both on-going and strategic). **Your role:** + Reviews QMS and Engineering changes as well as Quality plans to ensure ... quality for document control, records management, software validation, CAPA, Quality Planning, Management Review QMS processes; monitoring and assurance of… more
- L3Harris (Redmond, WA)
- …hypersonic propulsion. The Aerojet Rocketdyne Segment of L3Harris Technologies is seeking a senior-level Quality Engineer to serve as our AS9100 / ISO9001 QMS ... execution of a healthy CAPA process. + 45% - Perform Quality Management System ( QMS ) audits based on AS9100, ISO9001, customer and internal requirements. Plan,… more
