Bioprocess Associate

PE Global (UK)

Dunboyne

On-site

EUR 42,000 - 54,000

Full time

14 days+

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Job summary

A leading Biotech company in Meath is seeking a Manufacturing Bioprocess Associate for an 11-month contract position. This role involves operating equipment, working within a diverse team, and supporting manufacturing processes. The ideal candidate will have a science/engineering qualification and experience in GMP manufacturing. Interested candidates should submit a CV to apply.

Qualifications

  • 2+ years of experience in a GMP manufacturing environment required.
  • Experience with various single-use technologies in manufacturing.
  • Ability to work independently and in cross-functional teams.
  • Familiarity with contamination control and batch release requirements.

Responsibilities

  • Operate equipment according to electronic batch records and procedures.
  • Support weekend work to support manufacturing activities.
  • Author electronic batch records and sampling plans.
  • Maintain safety and compliance culture on site.
  • Assist authoring of electronic batch records, sampling plans, work instructions and SOPs.

Skills

Ability to work independently
Team collaboration
Familiarity with contamination control
Understanding of mAb manufacturing

Education

Level 6 qualification in a science or engineering discipline

Tools

Emerson DeltaV
Pas X

Job description

PE Global is currently recruiting for a Manufacturing Bioprocess Associate for a leading multi-national Biotech client based in Meath.

This is an initial 11-month contract position working on a 4-cycle shift pattern.

ROLE
  • Operate equipment according to electronic batch records, sampling plans and standard operating procedures.
  • Work as part of a multi-disciplined, diverse and dedicated process team where flexibility and teamwork are an essential requirement.
  • Support weekend or out of hours work on select time frames to support manufacturing activities.
  • Conduct all work activities with a strict adherence to the safety and compliance culture on site.
  • Support the authoring of electronic batch records, sampling plans, work instructions and standard operating procedures.
REQUIREMENTS
  • Level 6 qualification in a science or engineering discipline desired.
  • 2+ years’ experience in a GMP Manufacturing requirement shall be deemed equivalent.
  • Ability to work independently and within a cross‑functional team.
  • Familiarity with contamination control and batch release requirements.
  • Familiarity with Emerson DeltaV, Pas X, and the use of automation in a manufacturing process.
  • Experience with various single use technologies in a manufacturing environment.
  • Understanding of upstream and downstream unit operations for mAb manufacturing.

Interested candidates should submit an updated CV.

Please click the link below to apply, call Seán on +353 86 3514962 or alternatively send an up-to-date CV to sean.molloy@peglobal.net.

Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland.

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