崗位職責(zé):
1.According to the sales plan and weekly production plan, make the procurement plan of raw materials reasonably, control the purchase order, and improve the inventory turnover.
根據(jù)銷售計(jì)劃和每周生產(chǎn)計(jì)劃,合理制定原材料采購(gòu)計(jì)劃,控制采購(gòu)訂單,提高庫(kù)存周轉(zhuǎn)率。
2.Purchase raw materials, packaging materials and MRO according to purchasing SOP to ensure on-time delivery and meet the internal control standards and GMP requirement.
根據(jù)采購(gòu)SOP采購(gòu)原材料、包裝材料和MRO,確保準(zhǔn)時(shí)交貨,符合內(nèi)部控制標(biāo)準(zhǔn)和GMP要求。
3.Responsible for daily reconciliation with suppliers, payment application, accurate documents without errors.
負(fù)責(zé)與供應(yīng)商的日常對(duì)賬、付款申請(qǐng),確保準(zhǔn)確無(wú)誤。
4.Responsible for the draft and preliminary review of supplier contracts and other documents, including contract terms, price, payment terms, negotiations, and monitor the execution of contracts and delivery.
負(fù)責(zé)起草和初步審查供應(yīng)商合同和其他文件,包括合同條款、價(jià)格、付款條件、談判,并監(jiān)督合同的執(zhí)行和交付。
5.Supplier management, including supplier development, evaluation, audit and monthly/annual supplier performance review.
供應(yīng)商管理:包括供應(yīng)商開發(fā)、評(píng)估、審計(jì)和月度/年度供應(yīng)商績(jī)效審查。
6.Regular maintenance and analysis of procurement data, multi-channel collection of raw materials and packaging related to technology, quality, price and other information, in order to improve the quality of purchased materials, reduce costs.
定期維護(hù)和分析采購(gòu)數(shù)據(jù),多渠道收集原材料和包裝相關(guān)的技術(shù)、質(zhì)量、價(jià)格等信息,以提高采購(gòu)材料的質(zhì)量,降低成本。
7.According to CDMO project development plan, contact Headquarter or foreign suppliers to ensure on-time delivery of related goods or equipments as needed by projects.
根據(jù)CDMO項(xiàng)目發(fā)展計(jì)劃,聯(lián)系總部或國(guó)外供應(yīng)商,確保項(xiàng)目所需的相關(guān)貨物或設(shè)備按時(shí)交付。
8 Other tasks assigned by supervisor.
上級(jí)交辦的其他工作。
任職資格:
1.Bachelor degree or above,supply chain or related field.
本科以上學(xué)歷,供應(yīng)鏈或相關(guān)專業(yè)。
2.More than 5 years working experience in pharmaceutical company, familiar with GMP management process of pharmaceutical company.
五年以上制藥企業(yè)工作經(jīng)驗(yàn),熟悉制藥企業(yè)GMP管理流程。
3.CET-4 or above, with intermediate English reading and writing ability.
大學(xué)英語(yǔ)四級(jí)以上,具有良好的英語(yǔ)讀寫能力。
4.Familiar with ERP/U8 system.
熟悉ERP/U8系統(tǒng)。
5.Proficient in Office Word/Excel/PowerPoint and other software, strong data analysis ability.
熟練使用Word/Excel/PowerPoint等軟件,數(shù)據(jù)分析能力強(qiáng)。
6.Strong Interpersonal & Leadership skills.
較強(qiáng)的人際關(guān)系和領(lǐng)導(dǎo)能力。