出海雷达

MST合规支持专员

MST Compliance Support Specialist

开发工程限定地区(需当地身份)
公司Alvotech
薪资未公开
工作地点India
地域资格限定地区(需当地身份)
时区要求日间重叠约 6 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
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注意地域限制:该职位明确限定在 India 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。

Key responsibilities and minimum requirements according to job level:
· High level of independence and accountability for large projects and development within field.
· Performs variety of tasks of variable complexity.
· Takes part in large strategic projects.
· Challenges and decisions faced in the role are often non-precedent.
· Can have impact on large, important projects.
· Leading expert within field – guides and coaches' other employees.
Competencies required to fulfill the employee responsibilities and work assignments:
· An employee shall follow the job description that pertains to his/her position. In addition, an employee shall follow the SOPs that pertains to his/her position.
· An employee shall adhere to the company policies and procedures that are available on the Alvotech intranet – Alvocado.

The MST Compliance support specialist shall be responsible for:
· Establish MST Quality Record and Events (change control, manufacturing investigation etc.) management strategy, including specification and internal and external manufacturing related change controls
· Oversight and tracking of Quality Events (change controls, change actions, CAPA's, deviations, lab investigations) across MST, ensuring timely follow-up based on criticality and priority.
· Standardization of Quality Record and Events management processes- establishment and stanrdadization of the relevant processes and procedures and ensuring harmonized approach across the MST teams
· Cross Functional Collaboration - serve an alliance for compliance queries/issues with external and operational QA
· Represent MST in relevant review boards, e.g. Product Quality Complaints Review Board, OOS and Deviation Review Board, Control Strategy Review Board etc.
· Support in quality audits and due diligence activities
· Quality review of MST documents- Review MST reports against the relevant source documents and ensure alignment with cGMP strandards and internal compliance requirements
· SOP & Training Material Updates: Contribute to the revision and development of SOPs, training materials, and controlled documents based on process changes and campaign learnings.
· Cross-site matrix management and compliance overview of MST outsourced activities
· Serving as the one point of contact for all compliance related information and queries within MST
· Performing activities above and beyond their responsibilities as and when required

Minimum education and experience required for the role

  • Education: Bachelors/Master’s degree in a relevant discipline and direct industry experience or extensive experience in the pharmaceutical or biopharmaceutical sector.
  • Experience: Greater than 5 years international experience in Quality and/or Compliance Management in Biopharmaceutical or related industries. Demonstrated scientific and alliance management skills.

Originally 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。 本站只做信息聚合展示,不参与招聘流程,也不向求职者收取任何费用。

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