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Process Scientist

Job Overview

Process Scientist

Contract Type:

Full Time

Salary:

Location:

Sligo - Sligo

Contact Name:

Felicity Farrell

Industry:

Pharmaceutical & Medical Device

Date Published:

11-Jul-2025

Process Scientist

A leading biopharmaceutical client based in the Sligo region are looking for an experienced Process Scientist to join their small team.

Ideally you will have a minimum of 3 + years’ experience working within biopharmaceutical/pharma environment. You will have a broad knowledge of Biopharmaceutical /pharmaceutical manufacturing processes and experience in process validation.

Within this position you will play a crucial role in new product transfers, engineering runs, and process validations and contribute to the development of existing products. This is a non -laboratory based role.

The Position…

  • Permanent position
  • Highly attractive salary and benefits package on offer
  • Fantastic opportunity to join a growing and innovative organisation at an exciting stage of the business.
  • Friendly, inclusive and collaborative working environment. Teamwork and new ideas are very much encouraged.
  • Excellent opportunities for career progression and advancement.
  • Days only role – with WFH opportunities.

Responsibilities ( A snapshot…)

  • Execute new-product transfers, engineering runs, and process validations.
  • Provide technical support .
  • Lead new-process and cleaning validations, ensuring documentation compliance.
  • Monitor and optimize manufacturing processes, conducting root cause investigations for improvement.
  • Handle non-conformances, deviations, and change control requests.
  • Perform sample analysis in the laboratory.
  • Collaborate with cross-functional teams.

Requirements

  • Degree in a technical discipline (e.g., biochemistry, chemistry, biotechnology); master’s degree desirable.
  • Minimum 3-5 years in biotech/pharmaceuticals, GMP environment experience essential .
  • Knowledge of pharmaceutical manufacturing processes; experience in process validation.
  • Strong understanding of GMP, ICH, and compendia regulations.
  • Demonstrated ability in root cause analysis and effective investigation practices.
  • Excellent problem-solving, risk management, and decision-making skills.
  • Technical writing skills.
  • Proficient in English.

Next Steps:

APPLY!

Click Apply now to review the full details for this amazing opportunity or contact Felicity on 0867821714 for an informal chat.

APPLY NOW

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