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Scientist

Proclinical Speke 18.10.2026 Déposer ma candidature
Empresa
Proclinical
Lugar
Speke
Fecha
18.10.2026
Referencia
370055

Bridge Laboratory Innovation with Pilot-Scale Manufacturing

Join a dedicated team focused on the development and optimization of downstream processes for biopharmaceutical and vaccine products. This role offers a key opportunity to connect laboratory-scale experimentation with pilot plant operations, directly contributing to clinical programs and business milestones. It is an ideal position for individuals with hands-on experience in downstream purification who are eager to take technical ownership of processes while collaborating with senior scientists.

Key Responsibilities

  • Plan and execute laboratory and pilot-scale studies, focusing on downstream purification processes such as chromatography, filtration, and centrifugation.
  • Utilize statistical tools, such as Design of Experiments, to design, analyze, and interpret complex data sets, making informed decisions to guide project direction.
  • Author high-quality technical reports and documentation to ensure process knowledge is captured and transferable.
  • Maintain compliance with GxP standards during experimental execution and documentation, adhering to safety protocols and established systems of work.
  • Support laboratory housekeeping and monitor equipment readiness, including maintenance schedules and liaising with service providers.
  • Provide regular updates on project progress to stakeholders and contribute to knowledge-sharing initiatives within the team.
  • Collaborate with team members to meet project timelines and technical standards.

Essential Skills and Requirements

  • Degree in Biology, Biochemistry, or a related life sciences discipline.
  • Hands-on experience in downstream process development or manufacturing within the biopharmaceutical industry.
  • Proficiency in downstream techniques such as chromatography (e.g., FPLC, AKTA systems), tangential flow filtration (TFF), and depth filtration.
  • Familiarity with process scale-up and statistical analysis tools (e.g., JMP software).
  • Understanding of GxP standards and compliance requirements.
  • Strong technical reporting and communication skills.
  • Ability to work collaboratively in a team-oriented environment.

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