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Looking for an opportunity to bridge laboratory innovation with pilot-scale manufacturing and make a real impact on clinical programs?

̽»¨ºÏ¼¯ is seeking a dedicated Scientist to focus on the development and optimization of downstream processes for biopharmaceutical and vaccine products. You will play a key role in bridging laboratory-scale experimentation with pilot plant operations, contributing to clinical programs and business milestones. This is an excellent opportunity for individuals with hands-on experience in downstream purification who are eager to take technical ownership of processes while collaborating with senior scientists.

Responsibilities:

• Plan and execute laboratory and pilot-scale studies, focusing on downstream purification processes such as chromatography, filtration, and centrifugation.
• Utilize statistical tools (e.g., 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.

Key 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.

If you are having difficulty in applying or if you have any questions, please contact Numhom Sudsok at n.sudsok@proclinical.com.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

̽»¨ºÏ¼¯ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. ̽»¨ºÏ¼¯ is acting as an Employment Agency in relation to this vacancy.

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