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Alvotech Himalayas · Posted today

MST Compliance Support Specialist

Full time Remote

Compliance Specialist QA Specialist Pharmaceutical Compliance Quality Compliance Manager
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Indexed description

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

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