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As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people's lives.
Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology.
We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.
Global Operations -Global Operations is a complex and diverse organization within the company which is responsible for product fulfilment to all our customers from end to end.
We pride ourselves on being totally Customer Centric in our unrelenting focus on Improving Quality, Service and Value as perceived by our customers.
Our employees are dedicated to the Global Operations Enterprise Excellence journey.
Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients' lives.
Key Responsibilities:Implement QA activities as per established procedures and maintain compliance in the designated manufacturing areas and warehouses.
Supervise QA activity in designated manufacturing area and warehouse.
Ensure online activities are carried out as per procedure/specifications.
Ensure products are released on timely basis meeting customer and regulatory requirements.
Prepare and publish Quality analytical reports on timely basis.
Organize Quality meetings on regular basis with relevant departments.
Raise process non-conformance report or CAPA wherever required.
Support manufacturing in CAPA investigation and customer complaints whenever necessary.
Verify corrective actions for CAPA and follow up on effectiveness of corrective actions.
Train Senior Final Audit Supervisor (if applicable)/QA Auditors.
Highlight to QA Manager on unusual trends or defects.
Ensure the relevant procedures are reviewed and revised to current Quality System requirements.
Conduct internal audits/spot checks in production areas when required.
Ensure DHR is reviewed prior to final release and certification.
Ensure the implementation and maintenance within the workplace of an effective management for occupational safety and health consistent with the requirements of Occupational Safety and Health Act 1994 and other legislative requirements in the workplace.
Coordinate Quality Improvement Project.
Coordinate Ship Hold for the finished goods when required.
Review and verify shipment list and certificates.
Coordinate and monitor archiving DHR activity.
Control and release of product at Final Audit and Final Pack.
Work in hand with warehouse team in ensuring safe and good quality finished goods are distributed to customers.
Manage, coordinate and monitor soak test activity.
Note:As with all positions, due to the dynamic nature of Teleflex Medical business, key responsibilities may evolve and change over time.
Teleflex is an equal opportunities employer.
At Teleflex, we follow a comprehensive hiring process.
We do not accept unsolicited resumes from agency recruiters or 3rd party firms.
We do not make unsolicited job offers.
We do not ask for money or require equipment purchase up-front.
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Teleflex is a company that believes in values of Entrepreneurial Spirit, Building Trust and Make It Fun centered around People – our greatest asset.
We are the medical product division of Teleflex Incorporated, a large American MNC, manufacturing and distributing high quality health care products.
Our factory is located in Kamunting, Perak and we manufacture sterile disposable medical devices for the urology, anaesthesia and respiratory markets.
Our values are focused on customers, growth, leadership and people.#J-18808-Ljbffr