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QC Scientist (Product Testing & Stability)

Формат работы
onsite
Тип работы
fulltime
Английский
b2
Страна
UK
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Мэтч & Сопровод

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Описание вакансии

Текст:
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TL;DR
QC Scientist (Product Testing & Stability) (GMP/therapeutic proteins): Performing analytical testing and stability studies for therapeutic protein products in a regulated GMP laboratory with an accent on HPLC, capillary electrophoresis, spectrophotometry, and data interpretation. Focus on preparing stability documentation, leading quality investigations, and supporting CAPAs, change controls, and continuous laboratory improvement.

Location: Slough, United Kingdom; fully site-based

Company

hirify.global is a global life sciences company manufacturing medicines and therapeutic products across more than 30 sites.

What you will do

  • Perform GMP-compliant analytical testing of therapeutic protein samples using HPLC, capillary electrophoresis, spectrophotometry, and other physicochemical methods.
  • Review analytical data, assess results against specifications, identify trends, and communicate findings to Study Directors, Quality Assurance, and Manufacturing.
  • Prepare stability study protocols, testing summaries, and technical reports for product quality and stability programs.
  • Support deviations, investigations, CAPAs, and change controls, including leading routine quality investigations where appropriate.
  • Mentor colleagues, provide technical training, and promote best laboratory practices.
  • Support equipment monitoring, reagent and consumable management, housekeeping, and continuous improvement initiatives.

Requirements

  • Degree in Chemistry, Biochemistry, or another relevant scientific discipline, or equivalent laboratory experience.
  • Experience in a GMP-regulated pharmaceutical or biological laboratory.
  • Practical knowledge of HPLC, capillary electrophoresis, spectrophotometry, or other protein characterization methods.
  • Understanding of cGMP principles in a quality-controlled laboratory.
  • Strong analytical, problem-solving, organizational, and communication skills.
  • Commitment to quality, safety, continuous learning, and process improvement.

Culture & Benefits

  • Technical and professional development opportunities.
  • Collaborative, inclusive, and ethical working environment.
  • Competitive compensation and performance recognition.
  • Benefits relevant to the role and location.
  • Opportunities to contribute to continuous improvement and develop mentoring experience.

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