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MSD Bioprocess Associate 
Ireland, Dublin 
432145708

01.09.2024

Job Description

A fantastic opportunity has arisen for ain Upstream Operations.You will be responsible for all procedures and processes associated with the Manufacture of Commercial Large-Scale Drug Substance at the manufacturing facility.

The Bioprocess Associate will be responsible for the preparation, operation and monitoring of equipment, use of business systems and carrying out tasks including but not limited to the cleaning, validation, in-process testing and basic maintenance of equipment in accordance with current Good Manufacturing Practices (cGMPs).

Bring energy, knowledge, innovation to carry out the following:

  • Work with the manufacturing operations group, project design team, the CQV team, the Automation/CSV reps to facilitate the development and validation of the manufacturing facility.
  • Support Equipment Design/ HAZOP and Room programming reviews.
  • Support Operations team to consistently deliver on specific area Key Performance Indicators (KPIs), e.g. EHS metrics, Production Plan, OEE, compliance and team training.
  • Execute commercial manufacturing processes according to established work instructions and Standard Operating Procedures.
  • Generate SOPS/Electronic Batch Records.
  • Adhere to Right First-Time principals
  • Provide assistance and/or support maintenance, engineering, quality or other colleagues as requested.
  • Escalate issues as appropriate to Process Lead
  • Liaise with other groups and individuals to ensure planning of tasks is effective and linked into the manufacturing process plan.

What skills you will need:

In order to excel in this role, you will more than likely have:

  • Minimum of a Level 7 qualification in a science or engineering discipline.
  • A level 6 with a minimum of 3 years’ experience in a GMP Manufacturing requirement shall be deemed equivalent.
  • Team worker.
  • Ability to work cross functionally and with multiple stakeholders.
  • Trouble shooting capabilities.
  • Understanding of Drug Substance Manufacturing Operations.
  • Understanding of GMP requirements in a Bio-pharmaceutical Facility.
  • Excellent communication skills.
  • Ability to multi task

Please feel free to speak to us about what flexibility means to you during your application or click on the link to find out more about our

So, if you are ready to:

Invent solutions to meet unmet healthcare needs,please apply today.

Current Contingent Workers apply


Not Applicable


*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.



A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.