远程工作雷达

质量合规经理(欧洲集群)

Quality Compliance Manager (Europe Cluster)

其他限定地区(需当地身份)日间重叠约 2 小时,需偶尔早起或晚睡
公司未标注
薪资未公开
工作地点Germany
地域资格限定地区(需当地身份)
时区要求日间重叠约 2 小时,需偶尔早起或晚睡
用工类型permanent
发布时间2026-06-14
数据来源4dayweek.io
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注意地域限制:该职位明确限定在 Germany 招聘。如果你是位于中国大陆的求职者,通常需要当地工作身份才能投递,或需与雇主确认是否接受独立合同(Contractor)形式合作。
作息提示:日间重叠约 2 小时,需偶尔早起或晚睡。

加入EVA制药公司,这是一家致力于推动健康和福祉作为基本人权的领先制药公司。我们被公认为最佳工作场所,致力于为团队成员营造支持性强且富有创新性的环境。

职位概述

**质量合规经理(兼职)** 负责维护并持续改进德国质量管理系统(QMS),确保符合德国和欧盟药品法规。该职位负责质量流程、检查、审计、培训、供应商资质、CAPA管理以及对外部合作伙伴的质量监督,以确保组织始终保持检查准备状态并完全符合GxP要求。

#### 主要职责

- 维护并持续改进本地质量管理系统(QMS)。
- 管理质量文件,包括标准操作规程(SOP)、表格、记录和定期审查。
- 协调员工培训、资质计划和合规记录。
- 领导供应商、客户和服务提供商的资质活动。
- 计划、执行并跟进内部审计和质量评估。
- 管理偏差、质量事件、CAPA和流程改进项目。
- 监督与制造商、外部服务提供商和批次放行合作伙伴相关的质量接口。
- 准备、协调并支持监管机构的检查,同时确保持续的检查准备状态。

#### 工作类型

**兼职 | 远程办公(需在德国)**

查看英文原文

Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members.

Job Summary

The **Quality Compliance Manager (Part-Time)** is responsible for maintaining and continuously improving the German Quality Management System (QMS), ensuring compliance with German and EU pharmaceutical regulations. The role oversees quality processes, inspections, audits, training, supplier qualification, CAPA management, and quality oversight of external partners to ensure the organization remains inspection-ready and fully compliant with GxP requirements.

#### Key Responsibilities

- Maintain and continuously improve the local Quality Management System (QMS).
- Manage quality documentation, including SOPs, forms, records, and periodic reviews.
- Coordinate employee training, qualification programs, and compliance records.
- Lead supplier, customer, and service provider qualification activities.
- Plan, conduct, and follow up on internal audits and quality assessments.
- Manage deviations, quality events, CAPAs, and process improvement initiatives.
- Oversee quality-related interfaces with manufacturers, external service providers, and batch release partners.
- Prepare for, coordinate, and support regulatory authority inspections while ensuring ongoing inspection readiness.

#### Employment Type

**Part-Time | Remote (Germany-based)**

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