Downstream Process Development Scientist

5 days ago

Liverpool, Liverpool, United Kingdom Pharmaron Full time

We are seeking a highly skilled Downstream Development Scientist to join our team at Pharmaron.

About the Role:

  • Deliver and lead a wide range of activities associated with the design, development, scale-up, technical transfer, and validation of cGMP clinical manufacture of bulk drug substances.
  • Support project leads on delivery of both internal and client-based work packages.
  • Plan, design, deliver, and report activities within the laboratory, pilot plant, and/or production facility to meet project timelines.
  • Prepare and execute a range of documentation, including operating procedures, manufacturing records, and validation protocols.
  • Drive 5S and operational excellence initiatives to ensure a high-performing team.
  • Lead on the delivery of new capital equipment items and train others in procedures, techniques, equipment, and technologies.
  • Analyze investigation data to a high standard and ensure protocols and procedures are delivered with a high attention to detail.
  • Complete laboratory or batch-related documentation in a timely and compliant manner.
  • Be a subject matter expert in areas relating to GMP manufacture, upstream process development, downstream process development, or cell line development.
  • Provide periodic cover outside of normal working hours for essential operations.

About Us:

Pharmaron is a dynamic, fast-growing company with an enviable reputation for leading-edge science. We offer contract research services to some of the world's leading pharmaceutical companies, solving complex scientific challenges.

We believe in our ability to push forward the boundaries of scientific excellence, delivering solutions for our clients, always operating ethically and with integrity.

We take pride in our professionalism and commitment to delivering our very best work.

Our Liverpool site has a remarkable 20-year track record in biologics development, offering a fully integrated Gene Therapy Drug Substance Solution in our state-of-the-art cGMP facility.

We offer a competitive salary, a progressive and comprehensive suite of employee benefits, and the opportunity for growth and development.

Why Should You Apply?

  • This is an opportunity to make a real impact in a highly scientific and regulated environment, demonstrating leadership, ambition, and the desire to grow with the department.
  • Build and shape your career in an environment that sets and commits to the highest standards.
  • Be part of a team that supports each other, embraces and solves technical challenges, and puts excellence at the heart of all that we do.

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