Quality Control Supervisor (m/f/i) Heidelberg

 StepStone ·  12.01.2019 ·  Heidelberg ·  Becton Dickinson

BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. The company supports the heroes on the frontlines of health care by developing innovative technology, services and solutions that help advance both clinical therapy for patients and clinical process for health care providers. BD and its 65,000 employees have a passion and commitment to help improve patient outcomes, improve the safety and efficiency of clinicians’ care delivery process, enable laboratory scientists to better diagnose disease and advance researchers’ capabilities to develop the next generation of diagnostics and therapeutics. BD has a presence in virtually every country and partners with organizations around the world to address some of the most challenging global health issues. By working in close collaboration with customers, BD can help enhance outcomes, lower costs, increase efficiencies, improve safety and expand access to health care. In 2017, BD welcomed C. R. Bard and its products into the BD family. For more information on BD, please visit bd.com.The Quality Control Supervisor (m/f/i) reports to the Quality Manager and is responsible for managing and leading the QC department & team in Heidelberg. The ideal candidate achieves the desired results consistent with manufacturing objectives, internal and external quality standards, laws, directives, policies and procedures and ensures plant´s conformity with all legal and company requirements linked to his role. Furthermore, the Quality Control Supervisor (m/f/i) drives Continuous Improvement activities in all areas of his responsibility and improves QC´s overall effectiveness and efficiency. Further responsibilities are:

Preparing and implementing a budget linked to the role as well as ensuring compliance with the approved budget

Ensuring compliance with all legal requirements linked to the role like relevant BD policies, workforce health & safety laws and environmental standards

Implanting, maintaining and utilizing the “Manufacturing Engines” in QC

Establishing and maintaining appropriate forms and SOPs in compliance with GMP regulations, ISO, FDA requirements, Corporate and Plant Policies

Formal approval and release of products according approved quality and cost objectives

Complaint management process & vigilance observation

Accountability for investigation of root cause for any kind of product deviation as well as establishing appropriate corrective and preventive actions in time

Analysis of quality reports in cooperation with Production / QA

Ownership of the Quality- & Product-Review-Meetings

Ensuring predictable Product Flow and continuously improving the SAP Flow Metrics & QM Metrics results

Continuous support of R&D Manager as well as close cooperation with QA and production

You have a university degree in Biology as well as a minimum of 3-5 years’ experience in Microbiology. You have 3-5 years of experience in a management position with supervisory responsibility and profound knowledge of the European & US Pharmacopeia. Further requirements are:

Fluency in German and English

Profound knowledge of the IVD-Directive, MPG, ISO 13485

Collaboration in a highly motivated global environment. A familiar work climate in an innovative environment where your input counts. A safe workplace with long term perspectives. We endeavor a long term collaboration – hence corporate career planning throughout diverse phases of life conveys a high importance and value for us.

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