Nice to meet you ... If your company or group cares about "good for people", "solution systems" and ultimately "a better world", I would love to be part of it and work with you. My target is shaped to specialise in new technology focus, innovation, entrepreneurial approach and caring for people and accordingly the environment.If you would like to learn more about me, please read on. If you decide to find out more about me afterwards, please contact me directly by phone or e-mail. Thanks in advance.... After my academic education in Chemistry Department at Kocaeli University / TURKIYE, I started my career as a Quality Control Analyst in 'Ilsan-HEXAL' which was a well-known pharmaceutical company. Then continued as a Stability Analyst in 'Novartis-Sandoz' and responsible for the analysis and reporting of products stored under various conditions while maintaining GMP rules. Thanks to this duty, I had the chance to work in parallel with foreign guests at that times.When our Stability department was closed, I was pregnant with my daughter and decided to grow my baby. 2 years later, I came back again at Novartis-Sandoz and continued my career as a QC analyst, QA specialist and finally QA Training Coordinator. During this time period, I had enriched my career by gaining technical and administrative experiences in various ways such as GMP audits and thus internal and external audits, inspections, deviations, complaints, CAPAs and the development of an electronic training system. My last position in pharmaceutical industry was R&D and QA specialist at Santa Farma. I was responsible for identifying the actions to be taken and evaluating analytical data during the installation of the new production plant. I was also responsible for supporting qualification studies (which was new experience for me), participating in external audits, following the activities of the new plant and reporting the results through presentations and identifying the needs against non-conformity appeals.Now I am in the position of Quality manager in the Food Industry. Together with my team, we continue our quality-oriented studies within the scope of IFS and BRC for table olive, olive oil production, R&D studies. I am always open to offers that will open new doors and opportunities for me and my family.I wish you moments full of peace and smiles.Thanks for your interest.
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Quality Systems And Sales/Marketing ManagerSedi̇pi̇l Batarya Yenileme Ve Tasarım Merkezi Aug 2024 - Dec 2024Balıkesir, TürkiyeI had left my previous job to expand our customer portfolio to support (my husband) our own company related to ‘Renewable Energy Products Production’. My qualification is in the fields of Quality Control and Quality Assurance in the Pharmaceutical and Food industries both specialist and then executive.Yenilenebilir Enerji Ürünlerinin üretildiği firmamızda müşteri portföyünün genişletilmesine yönelik destek çalışmalarında yer aldım.
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Quality Assurance ManagerAnt Gida Aş_ Fora Zeytin Apr 2022 - Aug 2024Balıkesir, TürkiyeIn general trying to lead ensuring quality controls of the products from purchasing raw material to the shipment by providing all the requirements in terms of quality assurance with harmonious, dynamic and collaborative work with my team. Contributing improvement studies by making general controls of all process steps and work flows with my team. Also fulfill the requirements of the existing quality certificates while keeping track the necessary preparations and processes to obtain other relevant quality certificates. To assist and support our local and foreign customers in the quality issues they need. Besides follow the updates of the relevant legislation and standards. In addition follow the steps by setting targets to reduce the amount of emissions in sustainability studies. And reporting all of them to seniour management./Genel olarak takımımla beraber uyumlu, dinamik ve işbirlikçi çalışmalarla hammadde alımından sevkiyat aşamasına kadar ürünlerin kalite anlamında kontrollerinin ve kalite güvence anlamında da tüm gerekliliklerin sağlanmasında liderlik etmeye çalışmak. Üretimde alanların ve koşulların gıda güvenliği kapsamında her daim uygunluğunun sağlanması adına, iç denetimler yapma, eğitimler verilmesini sağlama ve uygulamaları takip etme gibi çalışmaları sürdürmek. Bu çalışmalar esnasında takımımla beraber tüm proses aşamalarının genel olarak kontrollerini yaparak iyileştirme çalışmalarına katkıda bulunmak. İlgili kalite belgelerinin alınması için gerekli hazırlık ve çalışma süreçlerini takip ederken var olan belgelerin gerekliliklerini de yerine getirmek. Gerek yerli gerekse yabancı müşterilerimizin ihtiyacı olan kalite konularında kendilerine yardımcı olmak ve gereken desteği sağlamak. İlgili mevzuatlar ve standartların güncellemeleri takip etmek. İlave olarak da sürdürülebilirlik çalışmalarına emisyon miktarlarını azaltıcı hedefler koyarak bu aşamaları takip etmek. Ve tüm çalışmaları üst yönetime raporlamak.
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R&D Specialist And Quality SpecialistSanta Farma Pharmaceuticals Sep 2014 - Sep 2015Gebze, Kocaeli, TürkiyeHere are some of my main responsibilities when I came first in Santa Farma;* especially responsible for product quality complaints handling,* performing internal and external audits and inspections,* improving QMEX system( deviation, customer complaint, training and documentation modules),* giving related QA trainings including GMP, for all the departments.After being a part of R&D Team which was generated for the new manufacturing plant, I was responsible to facilitate the Health Authority standards by developing and revising the quality system. During that period I was directly worked with top management, production, QC, warehouse, maintenance & engineering and HSE departments to achieve the company's targets.My responsibilities were;* supporting qualification studies for quality control lab. equipments by a consulting firm* following installation programmes of some production machines * controlling 44.000 m2 closed area, determining the needs and non-compliance objects in the scope of QA requirements,*tracking the actions*participating and reporting the audits*providing some KPI datas related with QC and QA, e.g. # of deviations and inspection actions, # of qualification studies, # of unperformed trainings and uncompleted procedures.*participating the weekly meetings to follow up the needs and actions thereby supporting the improvements about the related departments to achieve the quality targets.* organizing training plans for each department, giving trainings in time according to these plans and evaluating the effectivenesses of these trainings,* generating new procedures and keep tracking all the procedures and* being responsible from QA documentation. -
Training Coordinator And Quality Assurance SpecialistSandoz Novartis Jan 2012 - Sep 2014* to take role in implementation of a new training system, ‘Sandoz Electronic Learning System (SELS)’by collaborating Novartis Training Director and other stakeholders to improve both technically and in general manner.* to be the main responsible person of SELS in Gebze-1 and support every SELS user technically * to support departments’ training responsibles * to ensure the given trainings effectively* to generate a training matrix including all the departments * to determine departments’ training needs according to deviations, customer complaints, etc. for annual plans* to generate and organize QA training plans with annually * to give GMP and quality assurance trainings for all departments related with pharmaceutical operations in addition for new employees actively according to the annual plan * to help and support organizing departments’ training plans with their own superuser and track them.* to give information and training about SELS to superusers as SELS responsible person and also support technically, etc.* to participate internal and external audits presenting the new training systemAs a result to develop and manage SELS in Sandoz/Gebze1 and help to improve the training system.
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Quality Assurance SpecialistSandoz Novartis Sep 2010 - Jan 2012* to report the actions weekly and montly; present the charts and reports to management.* to follow CAPAs, control and confirm the finished ones.* to present internal and external inspections results.* to revise the procedures according to QMs and make GAP analysis.* to manage archiving system.* in the scope of technical changes to determine and confirm the changes only about infrastructure and engineering. Addition to this to support below (Quality Assurance Specialist 2010-2012) responsibilties where necessary.
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Quality Control SpecialistSandoz Novartis Jul 2006 - Mar 20102006 -2007 in TuzlaBy maintaining the GMP rules, analyzing the products which are reserved in various conditions like high temperature and humidty as well as reporting them. According to these I’d a chance to work paralel with foreing guests 2009-2010 in GebzeTuzla department was closed in 2007. At that time I was pregnant. After 2 years, I restarted at my current position again 2009 and continued to work until 2010.
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Quality Control AnalystIlsan Hexal Jun 2004 - Jul 2006By maintaining the GMP rules; * Preparing buffer solutions, mobile phase and also some kind of solvents * Testing the loss of moisture with Karl-Fisher instrument and drying train. * Measuring the physical characters of tablets and pellets * Doing some known test like extraction, titration and thin layer chromatography. * And reporting themThe common lab. Instruments: Sensitive assay balance and heavy balance, pH meter, ultrasonic bath, santrifuge instrument, drying train, magnetic mixer, shaker, distilled water inst., tablet hardness inst.• By maintaining the GMP rules; * Performing assay, impurity and dissolution analysis of tablets, pellets and syrups by using HPLC, UV-Vis * And reporting them.The Instruments: HPLC DAD – Agilent 1100 – 1200, HPLC – Waters, UV-Vis – Shimadzu 1700 (Wavelength 190 – 1100 nm. ) Dissolution - Sotax • By maintaining the GMP rules;Storing and keeping the records of coloumns of HPLC inst. ; necessary stock materials and also referance standarts in suitable temperatures. • By maintaining the GMP rules;* Doing validation operations in rare times* And reporting them• By maintaining the GMP rules;Doing calibration work of sensitive and heavy balance, pH meter, dissolution inst. and Karl – Fischer moisture inst.
Seda Seher Genç Education Details
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2,7/4 -
Fen - Matemati̇k
Frequently Asked Questions about Seda Seher Genç
What is Seda Seher Genç's role at the current company?
Seda Seher Genç's current role is Sales Manager (Satış ve Pazarlama Müdürü).
What schools did Seda Seher Genç attend?
Seda Seher Genç attended Kocaeli Üniversitesi, Istek Acıbadem Okulları.
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