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10 дней назад

Analytical Scientist (Biopharma)

54 800 - 73 067€
Формат работы
onsite
Тип работы
fulltime
Английский
b2
Страна
Ireland
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Analytical Scientist (Biopharma): Leading analytical development and Life Cycle Management projects for biologics manufacturing with an accent on critical process parameters, product quality attributes, and analytical control strategies. Focus on designing and transferring analytical methods, qualifying and validating processes, troubleshooting manufacturing and GMP activities, and driving continuous improvement.

Location: Waterford, Ireland; on-site

Salary: €54,800–€73,067 per year

Company

hirify.global is an R&D-driven, AI-powered biopharmaceutical company developing medicines and vaccines.

What you will do

  • Act as a specialist in critical process parameters and product quality attributes.
  • Lead analytical development and analytical/product Life Cycle Management projects.
  • Support analytical Life Cycle Management execution with Autonomous Production Units on a daily and weekly basis.
  • Report on analytical project progress and identify opportunities to improve site performance.
  • Collaborate with MSAT, Quality, Operations, Validation, Regulatory, program leads, and sister sites.
  • Support continuous improvement initiatives in MSAT Analytical and Quality Control.

Requirements

  • Degree in Biologics, Chemistry at NFQ Level 7 or 8, or a related scientific discipline.
  • Knowledge of lyophilisation and the monoclonal antibody sterile fill/finish context.
  • Experience leading analytical development projects covering research, design, implementation, transfer, qualification, and validation, applying design-for-manufacture principles.
  • Experience developing and implementing analytical control strategies.
  • Experience leading analytical qualification and validation activities.
  • Experience providing technical support, troubleshooting, and investigations for manufacturing and GMP activities.
  • Subject Matter Expert knowledge of analytical quality attributes and critical process parameters.
  • Experience leading analytical transfer projects.
  • Experience supporting experimental programmes, including pilot plant operations and studies.
  • Experience designing, executing, and implementing analytical development programmes and supporting MSAT Analytical teams on analytical development and product Life Cycle Management projects.

Culture & Benefits

  • Work on medicines and vaccines intended to improve lives worldwide.
  • Contribute to cutting-edge technology, resilient global supply, and more than 30 planned product launches by 2030.
  • Work in an inclusive environment with equal-opportunity principles.
  • Employees may be eligible for company benefit programmes.

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