英国负责人
Responsible Person UK
开发工程限定地区(需当地身份)
公司Oximio
薪资未公开
工作地点United States
地域资格限定地区(需当地身份)
时区要求日间重叠约 9 小时,基本正常作息
用工类型Full Time
发布时间8 天前
数据来源Himalayas
注意地域限制:该职位明确限定在 United States 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。
Category: Pharma/Biotech/Clinical Research
Location:
- EnsuringCompliance: The Responsible Person shall ensure that the wholesale distributionactivities carried out under the Wholesale Dealer's License comply with allapplicable laws, regulations, and guidelines related to the distribution,storage, and transportation of medicinal products
- Quality ManagementSystem: The Responsible Person shall establish and maintain an effectivequality management system for the wholesale distribution activities to ensureproduct quality and integrity are maintained at all times
- Record Keeping: The Responsible Person shallmaintain accurate and up-to-date records of all wholesale distributionactivities, including the receipt, storage, and supply of medicinal products
- Product Returns andRecalls: The Responsible Person shall manage product returns and recalls inaccordance with the relevant procedures and guidelines established by SMO UK
- ReportingObligations: The Responsible Person shall promptly report any suspected productdefects, incidents, or other significant issues related to the quality andsafety of the distributed products to SMO UK and MHRA as required by law
- Audits andInspections: The Responsible Person shall cooperate with the MHRA or any othercompetent authority concerning audits or inspections related to the wholesaledistribution activities conducted under the Wholesale Dealer's License
- Training andQualification: The Responsible Person shall ensure that personnel involved inwholesale distribution activities are appropriately trained and qualified fortheir respective roles
- ContinuousImprovement: The Responsible Person shall actively participate in continuousimprovement initiatives to enhance the effectiveness and efficiency of thewholesale distribution activities
- The RPi isresponsible for reviewing and approving import documentation, monitoring thequality of imported products, and investigating any complaints or qualityissues. The RPi also provides support with regulatory inspections
Requirements
Qualificationand Experience
Qualification
- Graduate qualification in Scientific, pharmaceutical,or related field
Experience
- The Responsible Person must have experience in thepharmaceutical industry
Skills, Knowledge, and Special Qualities
- Must be able to demonstrate that they have theknowledge and skills necessary to carry out their duties
- The ResponsiblePerson must also be able to work independently and be able to make decisions
Benefits
to be filled
DetailsOriginally posted on Himalayas
本页面信息整理自 Himalayas,版权归原发布方所有。职位可能随时关闭,投递请以原始页面为准。
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