Join Resmed as an Associate Manager, QC Operations and help lead our global quality control efforts across all production sites.
Responsibilities
- Lead and develop QC teams across all sites, review and support team members’ development, identify training needs and provide opportunities to broaden experience.
- Foster a culture of collaboration, safety, and continuous improvement within the QC function.
- Manage and optimize QC processes for incoming, production and global QC support, ensuring adherence to GMP, ISO and company quality standards.
- Coordinate incoming, in‑process and finished goods inspections, resolve quality issues using sound problem‑solving techniques.
- Ensure maintenance, filing and archiving of all inspection records are performed timely.
- Provide leadership and support to the calibration team to ensure compliance and maintenance of the Calibration Management System.
- Decide independently to ensure product conformity and strict adherence to quality procedures.
- Ensure nonconforming products are appropriately managed and investigate NCs in production with timely evaluation and disposition.
- Develop and deliver training in QC procedures and product specifications, keeping staff aware of new and revised documents.
- Improve existing QC processes and procedures related to in‑process and final inspection, and provide monthly reports and trending data against KPIs incorporating SPC.
- Serve as a subject‑matter expert for Quality Control operations in transformation initiatives, collaborating with global teams to ensure process alignment and consistency.
Qualifications and Experience
Build positive working relationships across the business to ensure QA is recognized as integral to business success and growth.Develop procedures, processes, metrics and systems to manage and monitor quality compliance.Identify and address barriers to continuous improvement.Analyze non‑conformance data and determine root cause and corrective actions.Demonstrate the ability to control and complete multiple issues with a clear sense of priority.Be self‑directing, self‑motivated and possess strong leadership and negotiation skills.Communicate excellently in writing and speaking, with keen attention to detail.Be computer literate in Microsoft Office, Oracle and other relevant software.Required
Degree in Engineering or a Science discipline with ISO standards training.At least 5 years’ experience in quality management positions within an ISO‑certified industry (pharmaceutical, medical devices or other highly regulated sectors).Preferred
ISO13485 Internal Auditor or Lead Auditor training.Joining us is more than saying “yes” to making the world a healthier place. It’s discovering a career that’s challenging, supportive, and inspiring. If this sounds like the workplace for you, apply now!
#J-18808-Ljbffr