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合同机会 - 高级OTC合规审计员(前FDA检查员的绝佳机会)

机器翻译
查看雇主原标题Contract Opportunity - Senior OTC Compliance Auditor (Great opportunity for former FDA Inspectors)

SGS · Remote, REMOTE, 美国

职位信息来自雇主公开的招聘页面。申请前请务必在雇主官网核实详情。

为什么值得关注?

发现指数 52/100,仅依据与该职位一起存储的证据计算。

52/100 发现指数
  • 新的雇主官方职位
  • 远程职位

分数构成

  • 时效性 (随职位发布时间变化)+18
  • 雇主官方来源+15
  • 远程职位+8
  • 稀有职位+3
  • 公司来源健康度+8

该职位未包含:已披露薪资、提及签证担保、提及搬迁、未出现在监控的职位板上。

这些理由来自雇主自己的职位描述与我们核实过的来源检查结果。除了已存储的信号之外,我们不做任何推测。

职位描述

英文原文

该职位由雇主以英文发布,暂无中文版本,下面完整显示英文原文。 查看官方职位页面.

职位描述

Company Description We are SGS – the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.

Job Description We are seeking a highly experienced Subcontractor – Senior OTC Compliance Auditor with a background as a former FDA Investigator/Inspector. This short-term assignment (May-August 2026) requires expertise in OTC drug manufacturing, cGMP compliance, and FDA inspection methodology. As a subcontractor, you will support audits, inspection readiness activities, and compliance reviews for clients in the OTC pharmaceutical industry.

岗位职责

• Conduct cGMP compliance audits of OTC drug manufacturing, packaging, labeling, and laboratory operations. • Apply FDA inspection methodology to identify compliance gaps, risks, and deficiencies. • Prepare detailed, professional audit reports outlining observations and recommended corrective actions. • Support clients with mock FDA inspections, inspection readiness activities, and compliance remediation. • Review quality systems, SOPs, batch records, data integrity controls, and laboratory practices. • Represent the organization professionally during international client engagements. • Manage scheduling, travel, and deliverables independently as an external contractor

任职要求

• Former FDA Investigator/Inspector (required). • 3–5 years of auditing experience within OTC or pharmaceutical manufacturing. • Strong understanding of cGMP requirements, OTC monograph expectations, and FDA enforcement practices. • Proven ability to conduct independent, high‑level audits and articulate findings clearly. • Excellent communication and technical writing skills. Travel • Must be willing and able to travel internationally, outside of North America, for the duration of the contract. Interested? If you’re a former FDA inspector with OTC auditing experience and open to a global contract assignment, we’d like to connect.

Additional Information SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression and Indigenous status, or any other characteristics protected by law. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required. This job description should not be construed as an exhaustive statement of duties, responsibilities, or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time. Accommodations are available on request for qualified candidates during each stage of the recruitment process. Please note that candidates applying for Canadian job openings should be authorized to work in Canada

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