Downstream Bio-Process Associate

QCS Staffing; Dublin; On-site; EUR 42,000 - 60,000; Full time

Job summary

QCS Staffing seeks a Downstream Bio-Process Associate for a 12-month contract in Dublin, Ireland. The role involves hands-on work in a major biopharma facility, coordinating with operations, CQV, and automation teams on design validation and documentation.

You will contribute to large-scale manufacturing processes, create SOPs, and navigate cGMP-style environments, with a 24/24 shift pattern offering exposure to continuous operations.

Qualifications

• Minimum Level 6 qualification in Engineering/Science, or equivalent regulated industry experience.
• Strong experience in a large-scale biopharmaceutical manufacturing facility.
• Experience with DeltaV and MES is advantageous.

Responsibilities

• Support project design and validation of the MPCC manufacturing facility with operations, CQV, and automation teams.
• Create SOPs and operating documentation for large-scale manufacturing.
• Execute commercial manufacturing processes per approved work instructions.
• This will be a 24/24 shift role.

Education

Level 6 qualification in Engineering/Science

Tools

DeltaV

MES

Job description

Downstream Bio-Process Associate - Ireland, Dublin - 12 Month Contract

Are you a Downstream Bio-Process Associate looking for your next challenge in Dublin? A leading multinational in Ireland’s thriving biopharma industry is expanding their team for a major facility development.

Downstream Bio-Process Associate - Ireland, Dublin - 12 Month Contract

Are you a Downstream Bio-Process Associate looking for your next challenge in Dublin? A leading multinational in Ireland’s thriving biopharma industry is expanding their team for a major facility development. This project provides hands‑on experience with innovative equipment, large‑scale operations, and modern pharmaceutical technologies. It’s an ideal opportunity to build your skills within one of Europe’s fastest‑growing life‑science regions.

What You’ll Do

• Working with the manufacturing operations group, project design team, the CQV team, & the Automation/CSV reps to facilitate the implementation of the project design and validation of the MPCC manufacturing facility.
• Creation of operating procedures & other relevant documentation for large scale manufacturing
• Execution of commercial manufacturing processes according to established work instructions.
• This will be a 24/24 shift role.

What you’ll need:

• The successful candidate will ideally possess a minimum of Level 6 qualification in an Engineering/Science related discipline; however, relevant experience in a similar regulated industry will also be considered (e.g. cGMP, ISO or similar cleanroom industry experience strongly preferred)
• Strong working experience in a large-scale biopharmaceutical manufacturing facility
• Experience with Delta V and MES would be considered an advantage.