£. RUDOLF, M. ROSZAK: EFFICIENCY OF THE PRODUCT-DEVELOPMENT PROCESS AS A FACTOR DETERMINING ... 429–431 EFFICIENCY OF THE PRODUCT-DEVELOPMENT PROCESS AS A FACTOR DETERMINING THE EFFECTIVENESS OF IMPLEMENTATION FOR SUBSEQUENT PROJECT PHASES ACC APQP U^INKOVITOST RAZVOJA PROCESA IZDELAVE KOT FAKTOR, KI DOLO^UJE USPE[NOST IZVEDBE KASNEJ[IH PROJEKTNIH FAZ PLANIRANJA KAKOVOSTI NAPREDNIH IZDELKOV (PKNI) £ukasz Rudolf * , Marek Roszak Silesian University of Technology, School of Doctors, Faculty of Mechanical Engineering, Department of Engineering Materials and Biomaterials, Stanis³awa Konarskiego 18A St., 44-100 Gliwice Prejem rokopisa – received: 2023-12-29; sprejem za objavo – accepted for publication: 2024-04-24 doi:10.17222/mit.2023.1085 This study presents a tool integrating PDCA Deming cycle and Design for Six Sigma principles to aid component development (especially dedicated for innovative projects). Designed for universal use across APQP (Advanced Product Quality Planning) phases, the tool guides through five key stages: Identify, Define, Design, Optimize, and Validate. Each stage involves specific actions and approvals, ensuring thorough development and risk assessment. Notably, the tool accommodates changing product requirements and validation challenges, allowing for adjustments without project delays. Its adaptability within the APQP framework is crucial for complex product development. The implementation at Tenneco demonstrates its effectiveness in struc- turing and overseeing development processes and improving project outcomes. Future analyses will delve into its impact and guide further research. Keywords: product development, PDAC, quality planning tools, change management Avtorja predstavljata {tudijo orodja za tako imenovano celovito na~rtovanje z Demingovim krogom »Planiraj-Naredi- Kontroliraj-Ukrepaj« (PDCA; angl.: Plan-Do-Check-Act) in oblikovanjem s {estimi sigma temelji (DSSP; angl..: Dsign for Six Sigma principles) kot pomo~ pri razvoju novih komponent ({e posebej namenjenih za inovativne projekte). Orodje je oblikovano za univerzalno uporabo preko faz kvalitetnega planiranja naprednih izdelkov (APQP; Advanced Product Quality Planning) in orodij ki vodijo skozi pet klju~nih stopenj ali faz: »Identificiraj, Definiraj, Oblikuj, Optimiziraj, Potrdi« (angl.: Identify, Define, Design, Optimize, and Validate). V vsako fazo so vklju~ena specifi~na dejanja oziroma akcije in presoje, ki zagotavljajo natan~en razvoj in oceno tveganja. Pomembno je, da je orodje prilagojeno eventualnim zahtevam po spremembi izdelka in izzivom njegove legalizacije, ne da bi pri tem pri{lo do zamud pri realizaciji projekta. Njegova prilagodljivost v okviru faz kvalitetnega planiranja naprednih izdelkov je odlo~ilna za razvoj kompliciranih izdelkov.Uporaba pri~ujo~ega orodja v firmi Tenneco je pokazala njegovo u~inkovitost v strukturiranju in nadzoru razvojnih procesov ter izbolj{anje rezultatov projekta. Prihodnje analize pa bodo pokazale njegov vpliv in vodilo za nadaljnje raziskave. Klju~ne besede: razvoj izdelka, metoda »planiraj-naredi-kontroliraj-ukrepa«j (PNKU), orodja za kvalitetno planiranje, sprememba upravljanja 1 INTRODUCTION Due to the high market demands for cars, manufac- turers associated with the automotive industry are ex- pected to minimize the time needed for product develop- ment and production, in parallel with the high expectations for reliability. In many cases, the correct implementation of the APQP methodology requires sup- port with additional planning tools aimed at increasing the efficiency of implementing subsequent phases of the APQP; this is particularly important in the case of new, innovative, complex products. 1–3 The result of the research conducted at Tenneco Au- tomotive Eastern Europe for the department responsible for the development of a product, such as an electroni- cally controlled shock absorber, is an original tool that systematizes actions and tasks that need to be taken to correctly define requirements, design, optimize and vali- date a new product. The fundamental goal was to design a universal planning tool regardless of the component or assembly being developed or modified. It was also essen- tial to use the designed tool irrespective of the phase of the APQP in which the project is located. 2 EXPERIMENTAL PART As part of the conducted research, a tool was created to support the development of a new component, assem- bly, or introducing changes to an existing one. The devel- oped tool is based on the concepts of the PDCA Deming cycle (Plan-Do-Check-Act) and Design for Six Sigma. A key priority during the design of the new tool was to en- able its universal and easy application, regardless of the Materiali in tehnologije / Materials and technology 58 (2024) 3, 429–431 429 UDK 330.341.1 ISSN 1580-2949 Original scientific article/Izvirni znanstveni ~lanek MTAEC9, 58(3)429(2024) *Corresponding author's e-mail: lukasz.rudolf@polsl.pl (£ukasz Rudolf) type of component being developed and the phase of APQP in which the project is currently located. 4.5 3 RESULTS The proprietary tool (presented in a simplified ver- sion in Figure 1) divides developing or modifying a component or assembly into 5 phases (Identity, Define, Design, Optimize, and Validate). Transition to the next phase requires completion and approval of specific ac- tions from the previous phase. The individual phases are characterized below: 1. IDENTIFY: A favourable decision to initiate the development process of a new component or introduce changes to an existing one. 2. DEFINE: Completing, analysing, and, where re- quired, quantifying the requirements for the new product. In this phase, the level of risk associated with developing £. RUDOLF, M. ROSZAK: EFFICIENCY OF THE PRODUCT-DEVELOPMENT PROCESS AS A FACTOR DETERMINING ... 430 Materiali in tehnologije / Materials and technology 58 (2024) 3, 429–431 Figure 1: Structured process for product development (own elaboration) Figure 2: Risk-Assessment tool, part of the product development process. Assessing potential development risks with four questions (own elabo- ration) a given part is also determined. The original Risk As- sessment tool is presented in Figure 2. 3. DESIGN: In a multifunctional team, develop a list of possible solutions and select the optimal one for the developed requirements. 4. OPTIMIZE: Clarifying technical details with the selected contractor. 5. VALIDATE: Component validation by the planned and approved plan. Using the new tool is particularly important when the product requirements change, or validation results are not acceptable; this requires changes to the product with- out affecting the accepted project schedule. The pro- posed solution aims to eliminate the possibility of omit- ting significant requirements and actions, which could negatively affect the project’s further implementation (timeliness and profitability). 6.7 4 DISCUSSION Besides structuring the product-development process, the proprietary solutions presented above allow its use in any phase of APQP, if necessary. This is important for products where development often goes beyond the stan- dard framework provided in the model approach, acc. to APQP. The tool is implemented and currently being tested. A detailed analysis of the results will constitute a separate study that will continue the solutions presented in this article. 5 CONCLUSIONS The product-development process, implemented at Tenneco as an additional tool supporting the already-im- plemented APQP process, changes the effectiveness of the project’s implementation (effectiveness of imple- menting subsequent phases acc. to APQP) by systematiz- ing the type and sequence of activities related to the de- velopment or modification of the component. Additionally, it is possible to monitor the level of risk as- sociated with individual product elements that are devel- oped in a systematized way and/or modified during the APQP process. Acknowledgment The study was created as a part of the doctoral stud- ies at the Joint Doctoral School covered by the program of the Ministry of Science and Higher Education "Imple- mentation doctorate". 6 REFERENCES 1 T. V. Tokmakova, V. I. Vysotskaya, E. N. 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