Formulation Production Manager
職位描述
ResponsibilitiesManage all PET activity including coordination of support staff, scheduling and continuous improvement * Understand operation process, perform self-evaluation and drive CI * Work directly with PET core team members to remove systemic obstacles that block our ability to achieve sustainable success * Advise and influence the development and/or adoption of lean tools * Producing resource planning and scheduling on a daily basisManage and control documentation and reports * Maintaining documentation that compliance to cGMPs, i.e.SOP, internal audit change control, training programme, deviation report and CAPA * Maintaining compliance to other regulatory * Maintaining compliance to SOXTypical People Management responsibility * Responsible for the process operation (here refer to OSD) within the PET, to defined process and operational standards. * Process Facilitators manage teams directly, or via Team Leaders. They are capable leaders and coaches. They manage performance & development of both the team and individuals. * Delivering hands-on coaching of multiple teams by daily meetings, planning, self-organizations, collaborations etc. * Facilitating frequent status meeting where the team member report to each other, commit to work and identify barriers * Expanding the understanding and practice of lean process and principles through the organization * Develop production team and operators capability through coaching, training program and task assignment etc * Communicate company policies & decisions within process group and ensure they are well understood and followed by staffResponsibility for GMP/Compliance/SHERequirements * Bachelor degree or above, major in Pharmaceutical engineering or chemical engineering. * 5 Years of working experience in related sector, 3 years above leadership role in MNC working experience * Pharma. Formulation knowledge on process, quality and regulatory * Team leadership and group process skills * Fluent English in reading, writing & speaking
企業簡介
阿斯利康是全球領先制藥公司,由前瑞典阿斯特拉公司和前英國捷利康公司于1999年合并而成。阿斯利康在6大治療領域為患者提供富于創新,卓有成效的醫藥產品,包括消化、心血管、腫瘤、中樞神經、麻醉和呼吸等,其中許多產品居于世界領先地位。
阿斯利康總部位于英國倫敦,研發總部位于瑞典。產品銷售覆蓋全球100多個國家和地區。2005年公司銷售收入為240億美元。
阿斯利康擁有強大的研發能力,平均每個工作日的研發投入達到1400萬美元 (2005年研發總投入為34億美元)。我們在7個國家設有11個研發機構,共有11,900名員工從事與新藥研發相關的工作。
阿斯利康擁有極具希望的早期開發產品組合,共有45個項目處于臨床前研究階段、17個項目處于一期臨床研究階段、13個項目處于二期臨床研究階段、6個項目處于三期臨床研究階段。
阿斯利康在全球19個國家有27個生產基地,共有14,000名員工致力于為客戶提供安全、有效、高質量的產品。
阿斯利康在全球共有65,000名員工,從事醫藥產品和醫療服務的研發、生產和銷售業務。
阿斯利康被列入道瓊斯可持續發展指數(全球)以及顯示企業良好社會責任度的富時社會責任指數(FTSE4Good Index)。
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職位發布日期: 2025-03-31