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DOVA Jobs Job Details - Process Scientist

Process Scientist

Thursday, may 07, 2020

Our client discovers, develops, manufactures and commercialises medicines, vaccines and diagnostic products, which are complemented by bio-devices, genetic tests and a range of services. They serve veterinarians, livestock producers and people who raise and care for farm and companion animals in more than 100 countries.

Randstad are recruiting for a 12 month contract for a Downstream Process Scientist to join their busy team based in Tullamore.


  • Competitive salary
  • Pension
  • Continuous learning and development
  • Holiday package

Education and Qualifications:

  • BSc, MSc or PhD in Chemical/Biochemical Engineering or related Biological Sciences with ³ 2 years of industrial experience.
  • Relevant experience in bioprocess development and/or purification processing.
  • Working in a controlled regulated environment e.g. GMP/GLP.
  • Knowledge of analytical methods required for protein characterisation.
  • Knowledge of key suppliers of process materials and equipment including disposable systems.
  • Excellent project management capability.
  • Excellent verbal and written communication skills. Ability to maintain very clear records of work completed.

Preferred Qualifications:

  • Knowledge and understanding of the workings of protein purification techniques using Unicorn software or similar automated control system.


  • Manufacture products using purification techniques: chromatography, ultrafiltration/ diafiltration and virus filtration.
  • Provide hands-on support for all manufacturing activities including purification processes, integrity testing, buffer / media preparation and cell culture.
  • Support the development, optimisation, scale-up, validation and commercial manufacture of a monoclonal antibody production processes.
  • Work with external partners to provide the necessary technical support for successful completion of projects including the transfer of processes into the facility.
  • Strict adherence to GMP, working in a cleanroom environment and executing batch records.
  • Support the writing and updating of Batch Manufacturing Records, SOPs, and other quality documents required for GMP manufacture.
  • Provide technical input and support writing of technical reports required for regulatory purposes.
  • Participate in Quality and Safety regulatory audits and completion of deviations and investigations into non-conformances.
  • Identify continuous improvement initiatives and action plans to implement operational excellence and lean practices.

Randstad Business Support acts as an employment business when supplying temporary staff and as an employment agency when introducing candidates for permanent employment with a client. Randstad Business Support is an equal opportunities employer and decisions are made on merits alone.

Job Reference:TM0520
Position Type:Contract
Sector:Biotechnology & Pharmaceutical, pharmaceutical
Working Hours:Full-Time
Location:Offaly, Offaly, Ireland
Contact:Samantha Reilly, Randstad Business Support, Belfast, United Kingdom
Phone:02890 912 840
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