Alvotech hf
Alvotech hf
Alvotech hf

Principal/ Senior Specialist Pharmaceutical Sciences Quality

Principal/ Senior Specialist Pharmaceutical Sciences Quality – Combination Products & Devices

Alvotech is looking for a new member to join Pharmaceutical Sciences Quality department. The department provides Quality and Compliance related support for multiple R&D activities across Alvotech sites. Potential candidate for this role understands the need for, and application of phase appropriate control across the development lifecycle within R&D, Quality Management System (QMS) and cGMP, with a specific focus on Combination Products and Devices (CPD).
Pharmaceutical Sciences (PharmSci) Quality (PSQ) is a function within R&D focused with quality oversight on development and validation activities at Alvotech across the development lifecycle.

Key Responsibilities:

  • Routinely leads cross functional projects and performs variety of tasks of variable complexity.
  • Collaborate with R&D partners in daily compliance activities and coach in executing quality related procedures.
  • Execute QA review and approval of various quality related documents generated by the CPD team (DHF, risk management files, and other associated documentation).
  • Review and approve procedures, and other supporting documents related to CPD processes.
  • Contribute as required in internal and health authority inspections and any other interactions with regulatory agencies.
  • Contribute as required in design of phase appropriate Quality Management System (QMS).


Qualifications:

  • Bachelor‘s/Master‘s degree in chemistry, biochemistry, biotechnology or equivalent.
  • Knowledge of Physiochemical/Bioanalytical methods, and Quality system processes such as CAPA, Change controls, Investigations, and document management, etc.
  • Minimum 5 years’ experience in Analytical quality assurance/quality management function in biopharmaceutical industry is desired.
  • Thorough understanding of regulatory GxP requirements and experience in supporting regulatory audits including FDA, and EMA.
  • Experience in using eDMS is an advantage.

    We offer a fun and challenging job in an international environment with diverse opportunities for professional development. If this exciting opportunity interests you, we invite you to explore further details on our website.

    We encourage you to visit our Career page (link: Join us - Alvotech - Better Access Better Lives) It offers valuable insights into our culture, values, and the innovative work we do.

Auglýsing birt15. maí 2025
Umsóknarfrestur31. maí 2025
Tungumálahæfni
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Staðsetning
Sæmundargata 15-19 15R, 101 Reykjavík
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