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社名社名非公開職種人事、労務業務内容-Own and execute core HR processes from onboarding to offboarding, including contract management, internalmobility, and data changes.-Collaborate closely with P&O Business Partners, Talent Acquisition, Payroll, Technology teams to ensureseamless employee experience.-Maintain accurate and up-to-date employee records in HCM systems (e.g., Workday, SAP/HR Core, SHAPEiN).-Ensure all transactions are documented in our Case Management System an

To be successful in this role, you will bring a "hands-on" approach to troubleshooting and a "big picture" mindset for process improvement.Qualifications & Experience:Electrical Trade Qualification (Essential).Experience: Minimum 5 years in FMCG, pharmaceutical, or a high-volume manufacturing environment.Leadership: Proven track record of leading and coaching a technical team.Technical Savvy: Strong knowledge of PLC’s, engineering design, and statutory saf

Plan, execute, and document Installation Qualification (IQ), Operational Qualification (OQ), andPerformance Qualification (PQ) activities for computerized systems and infrastructure supportingGMP/GxP operations. Ensure all validation activities are performed in accordance with approved procedures, industrystandards (e.g., ISPE GAMP 5), and regulatory expectations. Execute IQ/OQ protocols for IT infrastructure, including servers, networks, and laboratorys

about the company.A leading HKEX-listed biopharmaceutical groupabout the job.Lead the integration of internal control systems post-merger; establish and optimize policies covering the entire value chain (R&D, Manufacturing, and Sales).Develop risk indicators for asset operations and business processes; conduct regular risk identification, assessment, and early warning reporting.Organize and implement tasks for significant risk prevention and resolution; fo

社名社名非公開職種プロジェクトマネージャー、ディレクター業務内容This non-line management role functions as a strategic business partner within a pharmaceutical organization, dedicated to building an insights-led, data-driven culture alongside forecasting and analytics teams. The incumbent is responsible for leveraging quantitative and qualitative market research to inform strategic decisions, optimize market positioning, and ultimately drive profitability and growth. Additionally, the ro

Lifecycle Management Specialist ConsultantAre you a detail-oriented professional with a passion for pharmaceutical excellence? Join the J&J Innovative Medicine MSAT Large Molecule Drug Product team and play a pivotal role in ensuring the quality and compliance of primary packaging materials. This is your chance to manage critical lifecycles within a world-class manufacturing environment, driving innovation and stability in primary container systems.The Rol

Our client is an aesthetic company that partners with top brands to provide innovative skincare and medical aesthetic devices. They are seeking passionate individuals to join their team and contribute to making a positive impact. Reporting to: Sales Manager Location: JohorCompetitive salary and performance commission Work type: Hybrid The role:Drive sales growth and meet targets by promoting and selling aesthetics products to aesthetic doctors and skin spe

职位目标：全面负责工厂自动化系统（含生产、质检、仓储等相关自动化设备及控制系统）的规划、搭建、运维、优化及 团队管理工作。核心目标是保障自动化系统合规、稳定、高效运行，契合国际医药行业cGMP， ISPE等合规和 行业要求，提升生产效率、降低运营成本、保障产品质量，支撑企业生产销售业务的持续稳健发展，推动工厂 自动化、智能化升级。  工作职责：1、全生命周期管理：负责PLC、SCADA、MES、DCS等自动化系统的选型、安装调试、运维及故障排查，确保系统合规稳定运行 。2、合规与数据完整性：建立自动化系统SOP，确保符合cGMP、ISPE及数据完整性要求，涵盖审计追踪、备份恢复及账号管理 。3、项目统筹与升级：主导自动化相关项目的立项、预算、进度及验收，并根据行业趋势推动工厂的智能化升级与技术落地 。4、跨部门协作与审计：协调生产、质量等部门优化流程，并配合内部审计及NMPA、EMEA等外部监管检查 。5、成本与安全管控：制定并控制年度运维及项目预算，落实安全生产责任制，开展团队安全培训及隐患排查 。6、团

About company: A pre-IPO biotech Key Responsibilities:1) Regulatory CMC Strategy: Develop and execute comprehensive, proactive global CMC regulatory strategies for assigned programs from early development through marketing application and post-approval.Ensure strategies are aligned with regulatory requirements (FDA, EMA, PMDA, NMPA, etc.), corporate goals, and scientific development plans.2) Regulatory Submission Leadership: Serve as the Regulatory CMC Lea

工作职责 全面负责工厂自动化系统(含生产、质检、仓储等相关自动化设备及控制系统)的规划、搭建、运维、优化及团队管理工作核心目标是保障自动化系统合规、稳定、高效运行,契合国际医药行业 cGMP, ISPE 等合规和行业要求提升生产效率、降低运营成本、保障产品质量,支撑企业生产销售业务的持续稳健发展,推动工厂自动化、智能化升级与生产部、质量部、采购部、仓储部等相关部门保持密切沟通,协调解决自动化相关的跨部门协作问题,保障各环节工作衔接顺畅。领导自动化团队,指导和协调团队成员工作,提升团队能力,确保业务运作规范高效。任职要求 本科及以上学历,自动化、电气工程及其自动化、测控技术与仪器、过程装备与控制工程等相关专业;硕士学历优先。具备外资医药生产企业工作经验者优先,熟悉医药行业 GMP 合规要求,有医药工厂自动化管理经验者优先考虑。5-8 年及以上自动化相关工作经验,其中 3 年及以上团队管理经验,有医药工厂自动化团队管理经验者优先。具备自动化系统(PLC、SCADA、MES、DCS 等)的运维、优化及项目管理经验

公司介绍我的客户是一家专注于AAV基因治疗、mRNA及细胞治疗药物开发的生物制药公司。研发管线聚焦神经、眼科、代谢、罕见病、心衰、肿瘤等临床需求大、市场发展前景广的领域。公司拥有自主知识产权的腺病毒相关病毒(AAV)平台，建立了mRNA脂质体平台，拥有自主知识产权的mRNA递送系统和mRNA载体结构。瑞宏迪医药始终以健康为先，不断增强核心竞争力，保持开拓创新，为患者创造健康生活。岗位情况岗位名称：QA负责人（副总监/总监）汇报对象：质量负责人（Quality Head）管理团队：3-5人工作地点：广州-黄埔区主要职责负责领导以下职能团队完成相应的职能工作：负责药品全生命周期质量管理：从研发、工艺开发到临床阶段生产直至商业化生产的全面质量管理。负责全生命周期的生物药生产质量管理体系搭建与维护：制定并实施满足的质量管理体系，确保符合中美欧等市场的法律法规和技术指南。领导现场质量运营：监督生产活动，确保所有生产及运营活动符合既定的质量标准和规范。实验室合规支持：指导和支持QC团队进行分析实验室管理体系建设，确保检

about the company.A National Companyabout the team.Global Team about the job.RA headskills and experience required.8 years experience in Clinical RA 

GP Medical Representative – Western VICOur client is an ASX and NZX Listed Pharmaceutical leader, currently ranked in the Top 30 in Australia and the Top 10 in New Zealand. Their success is driven by a strong commitment to R&D, New Product Development, and the global out-licensing of proprietary products.Since their inception they have built a first-class reputation through high-quality products and a reliable salesforce that has never reduced headcount. W

The client is an early-stage company backed by leading investors and experienced biotech executives. Key Responsibilities:1. Lead the expression, purification, and characterization of antibody-based therapeutics (monospecifics, bispecifics, Fc fusions, and conjugates). 2. Drive innovation in biologics production — including heterodimerization control, conjugation (enzymatic, click, or linker-based), and modular payload formats (peptide, oligo, or protein).

岗位核心价值作为国际化车间负责人，您将全面负责冻干粉针剂生产线的运营管理。不仅要确保生产效率与成本目标的达成，更需构建符合 FDA、EMA 及 WHO 等国际主流标准的质量管理体系，引领车间通过并维持高标准的国际认证，支撑公司全球化战略的落地。 工作职责1. 卓越生产运营与现场管理全周期管理： 负责冻干粉针剂车间的年度生产计划落实，确保生产任务按时、保质、保量完成。工艺控制： 深度参与冻干工艺（Lyophilization）优化、无菌灌装工艺验证及培养基模拟灌装（Media Fill）等关键技术环节的监督。精益化管理： 引入精益生产（Lean Production）工具，优化工序衔接，降低物料损耗，提升 OEE（设备综合效率）。2. 国际化合规与审计体系法规转化： 动态跟踪 FDA、EMA、PIC/S 等国际最新法规与指南（如 Annex 1），主持车间内部差距分析（Gap Analysis），并制定落地整改计划。审计领航： 负责国际认证（如 FDA 现场检查、欧盟 QP 审计）的全流程管理，包括现场迎检、

关于企业.头部医药上市企业；关于团队.专业、和谐、多元化、包容；关于职位.1.SOX404合规项目管理：1）建立健全集团旗下境内及境外公司的内控体系，符合美国上市公司的监管要求：组织开展公司年度404合规工作的全流程，包括计划、实施、测试、整改及汇报；制定并维护公司年度内控流程更新及内控测试计划和时间表，带领团队确保项目按时高质量完成；管理内部控制矩阵（ICM）和流程文档（如流程描述、风险控制矩阵-RCM）的持续更新与优化。2）内控评估与测试：按照内控工作计划，带领团队实施内控设计有效性和运行有效性的自测；识别内控缺陷，起草内控评估报告，并提出切实可行的改进建议，组织相关部门开展内控缺陷整改和落实。2.风险评估及业务流程建设：进行公司层面风险评估以及业务风险排查，以风险为导向，在COSO框架的指引下，支持和协助业务部门搭建符合业务需求的流程框架；协调流程建设中存在的跨公司/部门协同问题，持续推动业务流程的改进与优化；3.内控专项审计：根据审计计划和公司管理要求，执行业务循环内控及IT内控专项审计项目，发现和

about the company.It is an integrated biopharmaceutical company focused on biosimilars and innovative antibodies for oncology and immune disorders.With a robust product portfolio and global R&D and commercial capabilities, it delivers high-quality biologics to patients worldwide.about the team.This fully integrated, in-house team drives efficient end-to-end innovation—from early discovery to global clinical development—consistently delivering best-in-class

The client is a listed company. Responsibilities:1.Design and perform physicochemical analytical support to biologics development from early to late stage.2.Analytical method development, transfer and troubleshooting for product quality control and stability study.3.Draft protocol/report and execute study to support IND/NDA filings.4.Participate in projects as ARD subject matter expert (SME) and provide professional guidance whenever needed.5.Continuously

Key Responsibilities:Lead and develop innovative global CMC regulatory strategies to ensure optimal development, registration, and lifecycle management of assigned products, balancing business objectives with regulatory compliance.Serve as the primary CMC regulatory subject matter expert (SME) on global project teams, providing clear, decisive guidance on regulatory risks and requirements.Interpret and apply global CMC regulations and guidelines (ICH, FDA,

Are you a results-driven sales professional with a passion for industrial products? Do you have a proven track record in expanding market share and building strong client relationships? We are seeking a dynamic Regional Sales Manager – AFD to spearhead the growth of our HVAC filtration product portfolio.Regional Sales Manager – AFDCompany OverviewWe are hiring for a leading organization specializing in industrial filtration solutions. We are committed to d

社名社名非公開職種メディカルアフェアーズ、学術業務内容MSLとして業務幅が広く、Medical戦略を実行に落とし込むための戦略立案に携わることができます臨床研究の窓口とり、Studyに携わることもできます求められる経験■Requirements・Advanced degree in life sciences (PhD, PharmD, MD) preferred.・Minimum 3 years of experience in the pharmaceutical or biotech industry.・Demonstrated experience in medical affairs or a related field within Oncology is strongly preferred.・Strong communication and presentation skills in both Japanese and English.・Experience working collabo

主要职责1.   根据原料药合成/工艺团队需求，协助制定并执行自动化实验方案，包括条件筛选、工艺优化等，按计划完成实验任务和数据整理。 2.   在既定项目方案下，负责自动化实验的具体操作与执行，包括设备上样、方法调用、运行监控及异常记录，初步进行数据分析与结果汇总。 3.   配合项目负责人准备项目汇报所需的实验记录、数据表格和图表，并参与与相关团队的日常沟通与对接。 4.   参与自动化平台及实验室的日常运营，包括设备排期、样品与试剂登记、数据与文档归档，协助维护实验室安全与SOP执行。 5.   协助完成设备日常检查、简单维护与问题反馈，配合同事及第三方进行故障排查和维护工作。 6.   持续学习自动化合成相关知识与工具，参与流程优化，提升平台运行效率。 任职资格1.   本科及以上学历，偏向于硕士2.   有1-2年制药行业自动化、机器人工作经验3.   偏向化学和自动化融合知识背景的人选4.   有机化学、药物化学、化学工程或自动化相关专业本科及以上学历，具备一定的有机合成或工艺化学基础，对基础工

公司介绍：一家pre-IPO阶段的biotech 岗位职责：1. 管理所承担项目的工艺开发内容，负责工作进度和工作质量，包括工艺研究方案设计， 方案执行监督和问题解决，工艺开发报告审核，工艺规程审阅，工艺批记录审阅，生产批 记录放行，合格供应商审计，生产现场核查、跟产，关键物料采购等与原料药工艺、生产 相关的工作。2. 负责管理生产计划，按要求交付物料，研究报告，协调上下游的进度。3. 负责撰写注册申报资料，协助完成申报工作。4. 负责寡核酸CMC工艺实验，包括工艺范围研究，工艺杂质研究等工艺性能研究项，起 草研究方案，完成实验并撰写研究报告。5. 负责维护寡核酸CMC工艺开发涉及的设备，包括SOP起草，修订，培训，设备常规维 护等实验室日常管理工作。6. 完成上级领导安排的其他工作。 任职资格：1. 硕士及以上学历，化学工艺背景，沟通能力良好。2. 10 年以上CMC工艺经验，有多个IND经历。3. 具备原料药工艺研发、生产管理经验.4. 优秀的Timeline 意识和英文沟通能力。5. 优秀的项目汇报和

about the company.A top vaccine biotechabout the team.RA teamabout the job.head of clinical raskills and experience required.10 years experience in global RA

about the company.A leading global oncology biotech founded in 2010, it now employs over 11,000 staff worldwide and has its products approved in more than 75 countries.about the team.Led by world-renowned scientific leaders and seasoned industry experts, the team integrates cutting-edge expertise in targeted therapies, immuno-oncology, and next-generation platforms (e.g., ADCs, CDACs).about the job.As a Principal Scientist in Physicochemical Analysis, you

about the company.One National Company about the team.Global Teamabout the job.PV Lead (PVP & PVO), directly report to Medical Leadskills and experience required.8 years plus industry working experience 

公司介绍：我的客户公司是一家专注于高端复杂制剂与精准靶向递送的领军级Biotech，深耕万亿级心脑血管慢病创新药赛道。核心技术源自国内顶级心血管专科医疗机构的科研转化，目前已完成数亿元规模融资，资金储备充裕。公司主导管线为全球首创（First-in-class）的靶向制剂，目前已实现中美双报并处于国际多中心临床阶段。管理团队由资深科学家与跨国药企工业化高管组成，北京研发总部与上海生产基地正加速推进商业化质量体系布局。职位名称：质量体系经理（无菌制剂）职位级别：经理-高级经理工作地点：上海-浦东新区管理团队：5人工作职责：1. 日常质量管理工作： a)    负责偏差管理工作：偏差发起，编号发放，初步评估，组织偏差调查会议（包括：DVRB/定期组织会议），审核相关调查评估，追踪确认纠正预防措施按时完成，有效性检查确认，相关记录保存归档； b)    负责变更管理工作：变更发起，变更编号发放，初步审核评估，组织变更讨论会议（包括：CCRB/定期组织会议），追踪行动项按时完成，变更有效性检查评估，相关记录保存归档

GP Medical Representative – Western VICOur client is an ASX and NZX Listed Pharmaceutical leader, currently ranked in the Top 30 in Australia and the Top 10 in New Zealand. Their success is driven by a strong commitment to R&D, New Product Development, and the global out-licensing of proprietary products.Since their inception they have built a first-class reputation through high-quality products and a reliable salesforce that has never reduced headcount. W

GP Medical Representative – Western VICOur client is an ASX and NZX Listed Pharmaceutical leader, currently ranked in the Top 30 in Australia and the Top 10 in New Zealand. Their success is driven by a strong commitment to R&D, New Product Development, and the global out-licensing of proprietary products.Since their inception they have built a first-class reputation through high-quality products and a reliable salesforce that has never reduced headcount. W

工作职责：采购职责范围： 临床前、临床服务采购。供应商信息收集与审核： 完善资料并持续优化供应商池。供应商准入管理与市场调研： 组织准入流程并进行市场调研更新信息。维护供应商关系： 日常维护，确保良好沟通和服务履行。供应商绩效管理： 评估绩效，反馈并跟进改进对策。供应商报价处理： 执行询价、比价、议价等。合同谈判与管理： 组织谈判、协助预算把控，审核费用。成本管理与控制： 寻找降本机会，保证采购价格的优势性。合同与保密协议管理： 编写、审批、签署、归档、执行跟进流程。采购策略制定： 制定品类采购策略。财务付款管理与成本控制： 处理发票核对与付款申请事宜。维护和更新采购数据： 确保采购记录和供应商信息的准确性。上级安排的其他工作。任职资格：8年及以上采购经验，有临床前或临床服务采购经验。 有团队管理经验优先。完整的采购流程、信息收集与判断能力、谈判能力、合同编写。 良好的谈判、人际沟通、团队协作能力。 责任心强，结果为导向，愿意与公司共同发展。