Biotech Production Supervisor — Shift Lead (cGMP)

Regeneron Pharmaceuticals, Inc

Munster

On-site

EUR 54,200 - 88,400

Full time

14 days+

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Benefits offered by this job

Job summary

Regeneron Pharmaceuticals, Inc. is seeking a Supervisor Biotech Production to join our Manufacturing team in Raheen, Limerick. The role offers an opportunity to lead a team responsible for commercial scale production of recombinant proteins in a cGMP environment.

You will supervise batch records, coordinate maintenance, schedule tasks, and mentor staff while upholding safety and quality standards. The position requires a BS/BA in Life Sciences and 5+ years of cGMP manufacturing experience with

Qualifications

  • Requires BS/BA in Life Sciences or related field with 5+ years of relevant cGMP manufacturing experience.
  • Experience in supervision/leadership roles.
  • Strong analytical and communication skills.

Responsibilities

  • Supervising commercial scale manufacturing of recombinant proteins in a cGMP environment.
  • Leading a team responsible for bulk drug substance production and ensuring schedules are met.
  • Reviewing and editing batch records in line with cGMP standards.
  • Ensuring availability of production batch records for upcoming lots and coordinating scheduling.
  • Overseeing equipment readiness, maintenance, and calibration; troubleshooting as needed.
  • Conducting cGMP audits of production areas and enforcing safety standards.
  • Managing people, including time sheets, vacations, training, and performance evaluations.
  • Interfacing with Facilities, Process Development, Regulatory, QA and QC.

Skills

Team leadership
cGMP manufacturing
Quality coordination
Batch records review
Problem solving
Communication skills

Education

BS/BA in Life Sciences or related field

Job description

Regeneron Pharmaceuticals, Inc. is seeking a Supervisor Biotech Production to join our Manufacturing team in Raheen, Limerick. The role offers an opportunity to lead a team responsible for commercial scale production of recombinant proteins in a cGMP environment.

You will supervise batch records, coordinate maintenance, schedule tasks, and mentor staff while upholding safety and quality standards. The position requires a BS/BA in Life Sciences and 5+ years of cGMP manufacturing experience with

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