- 1- Conducts in-departmental formulation, laboratory, stability and production trials studies regarding the development of new products and changes in existing products (cost reduction studies, essence changes, etc.) based on the demands of the marketing and private brands units.
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- 2- Controls and manages the documentation of all work under its management. For the products decided to be produced, it ensures that the signed formulas are submitted to the production and quality control departments or these formulas are submitted to the relevant departments for approval through the system.
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- 3- Periodically follows product innovations in the domestic and foreign markets and ensures comparisons (performance, cost, etc.) of existing products with competing products and informs its manager
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- 4- Coordinating to plan, conceptualize, and create electromechanical designs to improve the productivity and quality of the products.
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- 5- Manages the execution of innovative product development studies by examining innovations, trends and patent applications of product groups in the portfolio and working with relevant departments.
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- 6- It follows that the relevant tests (Dermatological, microbiological activity, claim tests, consumer tests, etc.) are carried out for the product to be placed on the market.
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- 7- Knowing the effects of production processes and technologies on the product and monitoring the formulation/raw material studies by evaluating them from this perspective.
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- 8- Defining the final version of product formulations/recipes into the system (SAP) and sharing them with the relevant units if necessary.
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- 9- The R&D Center monitors the execution of supported projects and the submission of articles / patent applications on relevant projects.
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- 10- Follows the solution process of material/raw material-related quality problems experienced in the process.
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- 11- Prepares input control and finished product analysis reports and relevant laboratory studies regarding alternative raw material studies with suppliers and presents them to the manager.
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- 12- Preparation of Product Information Files for final products to be put on the market, provision of Product Safety Assessment Reports, Control of MSDS and Formula Certificates, Control of Artwork works.
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- 13- Conducts department activities in accordance with GMP Rules.
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- 14- She/he also carries out other duties assigned to them by their superior in line with the purpose of the job
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- 15- Conducts department activities in accordance with GMP Rules.
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- 16- Acts in line with the QHSE Policies, and documentation of the department, takes environmental hazards, near misses, emergencies and accidents to the next level. He notifies his superior.
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- 17- Submits change requests in accordance with the procedure.
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