Downstream Process Development Scientist

4 weeks ago


Liverpool, Liverpool, United Kingdom Pharmaron Full time

Pharmaron is seeking a Downstream Process Development Scientist to contribute to the design, development, and scale-up of cGMP clinical manufacturing processes for bulk drug substances.

In this role, you will play a key part in ensuring the successful production of high-quality pharmaceutical products. You will work closely with a team of scientists and engineers to develop and optimize downstream processes, including purification, formulation, and characterization.

Key Responsibilities:

  • Lead the development and validation of cGMP manufacturing processes for bulk drug substances.
  • Plan, execute, and analyze experiments to optimize process parameters and improve product quality.
  • Prepare comprehensive documentation, including protocols, reports, and regulatory submissions.
  • Collaborate with cross-functional teams, including research scientists, engineers, and quality assurance personnel.
  • Stay abreast of industry best practices and emerging technologies in downstream processing.

Qualifications:

  • Bachelor's or Master's degree in a relevant life sciences or process engineering field.
  • PhD or equivalent industrial experience in bioprocess development, cGMP manufacturing, or process validation.
  • Proven experience in mammalian, microbial, or viral-based processes.
  • Strong analytical and problem-solving skills.
  • Excellent communication and interpersonal skills.


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