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Hľadanie poďľa názvu
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Product Quality Engineer (Sustaining Engineering Group)

Unomedical s.r.o.

Informácie o pracovnom mieste

Ponúkaný plat: - / - minimum 950€ / monthly (depending on experiences and quality of the candidate) + quarterly bonus and other benefits in compliance with social benefit program of the company

Termín nástupu: by agreement

Druh pracovného pomeru: full-time


Náplň práce, právomoci a zodpovednosti: • Representing Quality Management, actively contributes to the development of New Products within the new product development process. Responsible for ensuring that Design Control requirements including development of Design and Development plans meet regulatory and applicable procedural requirements. Responsible for reviewing and approving design control document outputs. Works closely with Manufacturing Quality Engineers to assure appropriate Validation Planning and a robust Design Transfer.
• Uses technical and GXP knowledge to influence and assure Quality and Compliance in Design and develops plans for Post Launch / lifecycle management activities.
• Provides leadership as subject expert in Design Control and actively supports and influences development teams in the translation of User Needs to Design Inputs, Design Outputs, Design Verification and Design Validation activities, and timely Design Reviews. Develops and assures that Quality Control Plans are complete and meet the standards and requirements appropriate for the type of product.
• Champions Risk Management activities through leadership, facilitation and active support during Product Development, and Post Launch Change Control activities. Demonstrates courage to drive Risk Management in decision-making to determine sound and timely decisions that balance compliance, business and product performance.
• Responsible for Post Launch Reviews. Investigates product / process performance issues and leads or participates in multifunctional evaluation of products in the market. Evaluates data using statistical tools. Leads or support Complaint investigations through Root Cause Analysis and effective Corrective or Preventive Actions (CAPA). Leads or actively supports Product Change Control.
• Performs internal and supplier process audits as required to support business. Uses auditing as a proactive tool for improvement as well as compliance and challenges existing practice where appropriate.
• Takes responsibility for the measuring and monitoring of performance against agreed KPIs. Collates and shares information / data through reports and follows up on identified improvement opportunities. Actively participates and / or drives site /Company wide Quality System improvements as required.

Iné výhody:

Požiadavky na zamestnanca

Požadované vzdelanie: University education (Master's degree)
Postgraduate (Doctorate)

Zameranie, odbor:
in Science or Engineering
Požadovaná prax: Prax na pozícii/v oblasti:


Počet rokov praxe:
3
Osobnostné predpoklady a zručnosti: • Degree or proven experience in science / engineering.
• Experience gained within a Regulated Industry, preferable Medical Devices.
• Demonstrated knowledge of Regulatory and ISO Compliance requirements. Good knowledge of Design Controls.
• Demonstrated knowledge and experience of Risk Management and the application and use of Risk Management Tools such as FMEA, Process Mapping, Hazard Analysis. ISO 14971
• Experience with Quality tools such as Quality Control Plans, Test Method validation and transfer, Statistics, Experimental Designs, Root Cause Analysis, Process validation, Process Optimization.
• Logical Thinking Skills and Experience: demonstrated ability to analyze and interpret complex problems / data gathered from a variety of sources and utilize.
• Demonstrated ability to effectively work and communicate in a cross-function, multinational environment building co-operative working relationships. Demonstrated ability to work effectively with multi-cultural and diverse suppliers and contract manufacturers.
• Good interpersonal skills and ability to influence people without direct authority.
• Proactive and flexible in adapting to changing environment and able to manage and prioritize work and competing objectives.
• Statistical knowledge, experience is desirable
• Six Sigma knowledge, experience and certification is preferable
• Advantage of experience of plastics, extrusion, injection moulding, assembly, bonding.
• Must be proficient with PC programs, statistical tools (e.g. Minitab) and MS Project and SAP knowledge is advantage

Inzerujúca spoločnosť

Stručná charakteristika spoločnosti: Spoločnosť Unomedical s.r.o. je súčasťou nadnárodnej spoločnosti ConvaTec, ktorá sa špecializuje na vývoj a výrobu jednorázových medicínskych pomôcok distribuovaných do nemocníc a centier zdravotnej starostlivosti po celom svete. Do portfólia výrobkov spoločnosti ConvaTec patria stomické pomôcky a prostriedky pre vlhké hojenie rán, s vlastnými vývojovými a výrobnými centrami a dlhoročnou tradíciou. Viac informácii je možné nájsť na www.convatec.sk.
Počet zamestnancov:
Adresa spoločnosti: Unomedical s.r.o.



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